{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,4]],"date-time":"2026-08-04T17:21:49Z","timestamp":1785864109048,"version":"3.56.0"},"reference-count":272,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2022,6,1]],"date-time":"2022-06-01T00:00:00Z","timestamp":1654041600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2022,6,1]],"date-time":"2022-06-01T00:00:00Z","timestamp":1654041600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2022,3,31]],"date-time":"2022-03-31T00:00:00Z","timestamp":1648684800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Neurobiology of Disease"],"published-print":{"date-parts":[[2022,6]]},"DOI":"10.1016\/j.nbd.2022.105718","type":"journal-article","created":{"date-parts":[[2022,4,4]],"date-time":"2022-04-04T20:45:48Z","timestamp":1649105148000},"page":"105718","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":30,"special_numbering":"C","title":["Synaptic alterations as a neurodevelopmental trait of Duchenne muscular dystrophy"],"prefix":"10.1016","volume":"168","author":[{"given":"Maria Egle","family":"De Stefano","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Valentina","family":"Ferretti","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chiara","family":"Mozzetta","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.nbd.2022.105718_bb0005","first-page":"1061","article-title":"A case of Becker muscular dystrophy with schizophrenia symptoms","volume":"42","author":"Abe","year":"1990","journal-title":"Brain Nerve"},{"key":"10.1016\/j.nbd.2022.105718_bb0010","first-page":"1","article-title":"Overview of gene therapy in spinal muscular atrophy and Duchenne muscular dystrophy","volume":"2020","author":"Abreu","year":"2020","journal-title":"Pediatr. Pulmonol."},{"key":"10.1016\/j.nbd.2022.105718_bb0015","first-page":"208","article-title":"Mental retardation in association with progressive muscular dystrophy","volume":"100","author":"Allen","year":"1960","journal-title":"Am. J. Dis. Child"},{"key":"10.1016\/j.nbd.2022.105718_bb0020","doi-asserted-by":"crossref","first-page":"4","DOI":"10.1093\/brain\/awf012","article-title":"Brain function in Duchenne muscular dystrophy","volume":"125","author":"Anderson","year":"2002","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2022.105718_bb0025","doi-asserted-by":"crossref","first-page":"280","DOI":"10.1016\/S0006-8993(03)03018-X","article-title":"Altered inhibitory input to Purkinje cells of dystrophin-deficient mice","volume":"982","author":"Anderson","year":"2003","journal-title":"Brain Res."},{"key":"10.1016\/j.nbd.2022.105718_bb0030","series-title":"Muscular Dystrophy","first-page":"91","article-title":"Duchenne muscular dystrophy and brain function","author":"Anderson","year":"2012"},{"key":"10.1016\/j.nbd.2022.105718_bb0035","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1177\/1756286419845567","article-title":"Advances in imaging of brain abnormalities in neuromuscular disease","volume":"12","author":"Angelini","year":"2019","journal-title":"Ther. Adv. Neurol. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0040","doi-asserted-by":"crossref","first-page":"492","DOI":"10.1006\/bbrc.1997.7328","article-title":"Targeted disruption of exon 52 in the mouse dystrophin gene induced muscle degeneration similar to that observed in Duchenne muscular dystrophy","volume":"238","author":"Araki","year":"1997","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"10.1016\/j.nbd.2022.105718_bb0045","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1186\/s12868-017-0381-0","article-title":"Myelination is delayed during postnatal brain development in the mdx mouse model of Duchenne muscular dystrophy","volume":"18","author":"Aranmolate","year":"2017","journal-title":"BMC Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0050","doi-asserted-by":"crossref","first-page":"168","DOI":"10.1016\/j.ridd.2015.07.025","article-title":"Reading impairment in Duchenne muscular dystrophy: A pilot study to investigate similarities and differences with developmental dyslexia","volume":"45-46","author":"Astrea","year":"2015","journal-title":"Res. Dev. Disabil."},{"key":"10.1016\/j.nbd.2022.105718_bb0055","doi-asserted-by":"crossref","first-page":"187","DOI":"10.1016\/S0960-8966(99)00105-4","article-title":"Expression and synthesis of alternatively spliced variants of Dp71 in adult human brain","volume":"10","author":"Austin","year":"2000","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0060","doi-asserted-by":"crossref","first-page":"433","DOI":"10.1016\/j.mcn.2008.12.011","article-title":"Truncated dystrophins can influence neuromuscular synapse structure","volume":"40","author":"Banks","year":"2009","journal-title":"Mol. Cell. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0065","doi-asserted-by":"crossref","first-page":"3195","DOI":"10.1167\/iovs.13-11700","article-title":"ON and OFF electroretinography and contrast sensitivity in Duchenne muscular dystrophy","volume":"54","author":"Barboni","year":"2013","journal-title":"Invest. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.nbd.2022.105718_bb0070","doi-asserted-by":"crossref","first-page":"3581","DOI":"10.1167\/iovs.16-19287","article-title":"Dystrophin Is required for proper functioning of luminance and red\u2013green cone opponent mechanisms in the human retina","volume":"57","author":"Barboni","year":"2016","journal-title":"Invest. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.nbd.2022.105718_bb0075","doi-asserted-by":"crossref","first-page":"897","DOI":"10.1016\/S0140-6736(98)05801-2","article-title":"Absence of brain Dp140 isoform and cognitive impairment in Becker muscular dystrophy","volume":"353","author":"Bardoni","year":"1999","journal-title":"Lancet"},{"key":"10.1016\/j.nbd.2022.105718_bb0080","doi-asserted-by":"crossref","first-page":"194","DOI":"10.1016\/S0960-8966(99)00108-X","article-title":"Loss of Dp140 regulatory sequences is associated with cognitive impairment in dystrophinopathies","volume":"10","author":"Bardoni","year":"2000","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0085","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1016\/j.nmd.2021.01.011","article-title":"Longitudinal data of neuropsychological profile in a cohort of Duchenne muscular dystrophy boys without cognitive impairment","volume":"31","author":"Battini","year":"2021","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0090","first-page":"54","article-title":"Exploring the molecular basis for variability among patients with Becker Muscular Dystrophy: dystrophin gene and protein studies","volume":"49","author":"Beggs","year":"1991","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.nbd.2022.105718_bib1382","doi-asserted-by":"crossref","first-page":"954","DOI":"10.1002\/glia.23941","article-title":"Dp71 contribution to the molecular scaffold anchoring aquaporine-4 channels in brain macroglial cells","volume":"69","author":"Belmaati Cherkaoui","year":"2021","journal-title":"Glia"},{"key":"10.1016\/j.nbd.2022.105718_bb0095","doi-asserted-by":"crossref","DOI":"10.1016\/j.mcn.2020.103482","article-title":"Hippocampal synaptic and membrane function in the DBA\/2J-mdx mouse model of Duchenne muscular dystrophy","volume":"104","author":"Bianchi","year":"2020","journal-title":"Mol. Cell. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0100","doi-asserted-by":"crossref","first-page":"371","DOI":"10.1016\/S0960-8966(06)80008-8","article-title":"Cognitive functions in Duchenne muscular dystrophy: a reappraisal and comparison with spinal muscular atrophy","volume":"2","author":"Billard","year":"1992","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0105","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1111\/j.1469-8749.1998.tb15351.x","article-title":"Reading ability and processing in Duchenne muscular dystrophy and spinal muscular atrophy","volume":"40","author":"Billard","year":"1998","journal-title":"Dev. Med. Child Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0110","doi-asserted-by":"crossref","first-page":"1203","DOI":"10.1002\/glia.22317","article-title":"Aquaporin-4 and epilepsy","volume":"60","author":"Binder","year":"2012","journal-title":"Glia"},{"key":"10.1016\/j.nbd.2022.105718_bb0115","doi-asserted-by":"crossref","first-page":"92","DOI":"10.1016\/S0166-2236(99)01510-6","article-title":"The neurobiology of Duchenne muscular dystrophy: learning lessons from muscle?","volume":"23","author":"Blake","year":"2000","journal-title":"Trens Neurosci"},{"key":"10.1016\/j.nbd.2022.105718_bb0120","doi-asserted-by":"crossref","first-page":"241","DOI":"10.1073\/pnas.95.1.241","article-title":"Beta-dystrobrevin, a member of the dystrophin-related protein family","volume":"95","author":"Blake","year":"1998","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.nbd.2022.105718_bb0125","doi-asserted-by":"crossref","first-page":"645","DOI":"10.1083\/jcb.147.3.645","article-title":"Different dystrophin-like complexes are expressed in neurons and glia","volume":"147","author":"Blake","year":"1999","journal-title":"J. Cell Biol."},{"key":"10.1016\/j.nbd.2022.105718_bb0130","doi-asserted-by":"crossref","first-page":"291","DOI":"10.1152\/physrev.00028.2001","article-title":"Function and genetics of dystrophin and dystrophin-Related proteins in muscle","volume":"82","author":"Blake","year":"2002","journal-title":"Physiol. Rev."},{"key":"10.1016\/j.nbd.2022.105718_bb0140","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0002084","article-title":"Muscle dystroglycan organizes the postsynapse and regulates presynaptic neurotransmitter release at the Drosophila neuromuscular junction","volume":"3","author":"Bogdanik","year":"2008","journal-title":"PLoS One"},{"key":"10.1016\/j.nbd.2022.105718_bb0145","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1016\/0960-8966(94)90072-8","article-title":"Cognitive impairment in Duchenne muscular dystrophy","volume":"4","author":"Bresolin","year":"1994","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0150","doi-asserted-by":"crossref","first-page":"164","DOI":"10.3389\/fnmol.2020.00164","article-title":"Dystroglycan mediates clustering of essential GABAergic components in cerebellar Purkinje cells","volume":"13","author":"Briatore","year":"2020","journal-title":"Front. Mol. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0155","doi-asserted-by":"crossref","first-page":"4805","DOI":"10.1523\/JNEUROSCI.22-12-04805.2002","article-title":"GABAergic terminals are required for postsynaptic clustering of dystrophin but not of GABA(A) receptors and gephyrin","volume":"22","author":"Brunig","year":"2002","journal-title":"J. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0160","doi-asserted-by":"crossref","first-page":"551","DOI":"10.1007\/BF01799614","article-title":"Genetic and clinical correlation of Xp21 muscular dystrophy","volume":"15","author":"Bushby","year":"1992","journal-title":"J. Inherit. Metab. Dis."},{"key":"10.1016\/j.nbd.2022.105718_bb0165","doi-asserted-by":"crossref","first-page":"257","DOI":"10.1016\/j.expneurol.2007.02.015","article-title":"The sarcoglycan complex in Schwann cells and its role in myelin stability","volume":"205","author":"Cai","year":"2007","journal-title":"Exp. Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0170","doi-asserted-by":"crossref","first-page":"911","DOI":"10.1016\/j.nmd.2017.07.008","article-title":"DMD and West syndrome","volume":"27","author":"Cardas","year":"2017","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0175","doi-asserted-by":"crossref","first-page":"213","DOI":"10.1016\/S0006-8993(01)02108-4","article-title":"The organisation of spinal projecting brainstem neurons in an animal model of muscular dystrophy. A retrograde tracing study on mdx mutant mice","volume":"895","author":"Carretta","year":"2001","journal-title":"Brain Res."},{"key":"10.1016\/j.nbd.2022.105718_bb0180","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0230083","article-title":"Characterization of brain dystrophins absence and impact in dystrophin-deficient Dmdmdx rat model","volume":"15","author":"Caudal","year":"2020","journal-title":"PLoS One"},{"key":"10.1016\/j.nbd.2022.105718_bb0190","doi-asserted-by":"crossref","first-page":"21","DOI":"10.2478\/bjmg-2013-0014","article-title":"Association between loss of dp140 and cognitive impairment in Duchenne and Becker dystrophies","volume":"16","author":"Chamova","year":"2013","journal-title":"Balkan J Med Genet"},{"key":"10.1016\/j.nbd.2022.105718_bb0195","doi-asserted-by":"crossref","first-page":"111","DOI":"10.1016\/j.nlm.2015.07.006","article-title":"Cognitive dysfunction in the dystrophin-deficient mouse model of Duchenne muscular dystrophy: a reappraisal from sensory to executive processes","volume":"124","author":"Chaussenot","year":"2015","journal-title":"Neurobiol. Learn. Mem."},{"key":"10.1016\/j.nbd.2022.105718_bb0200","doi-asserted-by":"crossref","first-page":"2670","DOI":"10.1007\/s12035-018-1259-6","article-title":"Dp71-dystrophin deficiency alters prefrontal cortex excitation-inhibition balance and executive functions","volume":"56","author":"Chaussenot","year":"2019","journal-title":"Mol. Neurobiol."},{"key":"10.1016\/j.nbd.2022.105718_bb0205","doi-asserted-by":"crossref","first-page":"1219","DOI":"10.1097\/00001756-200207020-00030","article-title":"Genetically dystrophic mdx\/mdx mice exhibit decreased response to nicotine in passive avoidance","volume":"13","author":"Coccurello","year":"2002","journal-title":"Neuroreport"},{"key":"10.1016\/j.nbd.2022.105718_bb0215","doi-asserted-by":"crossref","first-page":"802","DOI":"10.1016\/j.neuint.2009.08.003","article-title":"Oxidative variables and antioxidant enzymes activities in the mdx mouse brain","volume":"55","author":"Comim","year":"2009","journal-title":"Neurochem. Int."},{"key":"10.1016\/j.nbd.2022.105718_bb0220","doi-asserted-by":"crossref","first-page":"66","DOI":"10.1016\/j.neulet.2009.04.065","article-title":"Striatum brain-derived neurotrophic factor levels are decreased in dystrophin-deficient mice","volume":"459","author":"Comim","year":"2009","journal-title":"Neurosci. Lett."},{"key":"10.1016\/j.nbd.2022.105718_bb0225","doi-asserted-by":"crossref","first-page":"359","DOI":"10.1016\/j.nmd.2011.02.017","article-title":"Reduction of acethylcolinesterase activity in the brain of mdx mice","volume":"21","author":"Comim","year":"2011","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0230","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1002\/mus.24704","article-title":"Activity of Krebs cycle enzymes in mdx mice","volume":"53","author":"Comim","year":"2016","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.nbd.2022.105718_bb0235","doi-asserted-by":"crossref","first-page":"n7608","DOI":"10.1007\/s12035-019-1573-7","article-title":"Neurocognitive impairment in mdx mice","volume":"56","author":"Comim","year":"2019","journal-title":"Mol. Neurobiol."},{"key":"10.1016\/j.nbd.2022.105718_bb0240","doi-asserted-by":"crossref","first-page":"28387","DOI":"10.1074\/jbc.M402604200","article-title":"The potassium channel Kir4.1 associates with the dystrophin-glycoprotein complex via \u03b1-Syntrophin in glia","volume":"279","author":"Connors","year":"2004","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.nbd.2022.105718_bb0245","doi-asserted-by":"crossref","first-page":"94","DOI":"10.1111\/j.1528-1157.1989.tb05289.x","article-title":"Prevalence of epilepsies in children and adolescents","volume":"30","author":"Cowan","year":"1989","journal-title":"Epilepsia"},{"key":"10.1016\/j.nbd.2022.105718_bb0250","doi-asserted-by":"crossref","first-page":"141","DOI":"10.1186\/s13023-020-01430-8","article-title":"Global epidemiology of Duchenne muscular dystrophy: an updated systematic review and meta-analysis","volume":"15","author":"Crisafulli","year":"2020","journal-title":"Orphanet J. Rare Dis."},{"key":"10.1016\/j.nbd.2022.105718_bb0255","doi-asserted-by":"crossref","first-page":"486","DOI":"10.1016\/j.neubiorev.2007.09.001","article-title":"Duchenne muscular dystrophy: a cerebellar disorder?","volume":"32","author":"Cyrulnik","year":"2008","journal-title":"Neurosci. Biobehav. Rev."},{"key":"10.1016\/j.nbd.2022.105718_bb0260","doi-asserted-by":"crossref","first-page":"474","DOI":"10.1016\/j.jpeds.2006.12.045","article-title":"Delayed developmental language milestones in children with Duchenne\u2019s muscular dystrophy","volume":"150","author":"Cyrulnik","year":"2007","journal-title":"J. Pediatr."},{"key":"10.1016\/j.nbd.2022.105718_bb0265","doi-asserted-by":"crossref","first-page":"853","DOI":"10.1017\/S135561770808106X","article-title":"Cognitive and adaptive deficits in young children with Duchenne muscular dystrophy (DMD)","volume":"14","author":"Cyrulnik","year":"2008","journal-title":"J. Int. Neuropsychol. Soc."},{"key":"10.1016\/j.nbd.2022.105718_bb0270","doi-asserted-by":"crossref","first-page":"635","DOI":"10.1016\/j.nbd.2011.05.012","article-title":"Rescue of a dystrophin-like protein by exon skipping normalizes synaptic plasticity in the hippocampus of the mdx mouse","volume":"43","author":"Dall\u00e9rac","year":"2011","journal-title":"Neurobiol. Dis."},{"key":"10.1016\/j.nbd.2022.105718_bb0275","doi-asserted-by":"crossref","first-page":"3779","DOI":"10.1093\/hmg\/ddp320","article-title":"Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression","volume":"18","author":"Daoud","year":"2009","journal-title":"Hum. Mol. Genet."},{"issue":"8","key":"10.1016\/j.nbd.2022.105718_bb0280","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0006574","article-title":"Role of mental retardation-associated dystrophin-gene product Dp71 in excitatory synapse organization, synaptic plasticity and behavioral functions","volume":"4","author":"Daoud","year":"2009","journal-title":"PLoS One"},{"key":"10.1016\/j.nbd.2022.105718_bb0285","doi-asserted-by":"crossref","first-page":"466","DOI":"10.1002\/mus.26803","article-title":"Neurodevelopmental, behavioral, and emotional symptoms common in Duchenne muscular dystrophy","volume":"61","author":"Darmahkasih","year":"2020","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.nbd.2022.105718_bb0290","doi-asserted-by":"crossref","first-page":"762","DOI":"10.1038\/nrm2024","article-title":"Molecular mechanisms of muscular dystrophies: old and new players","volume":"7","author":"Davies","year":"2006","journal-title":"Nat. Rev. Mol. Cell Biol."},{"key":"10.1016\/j.nbd.2022.105718_bb0295","doi-asserted-by":"crossref","first-page":"480","DOI":"10.1038\/ejhg.2013.169","article-title":"A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy","volume":"22","author":"de Brouwer","year":"2014","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.nbd.2022.105718_bb0300","doi-asserted-by":"crossref","first-page":"613","DOI":"10.1016\/S0306-4522(97)00003-1","article-title":"Dystrophin and its isoforms in a sympathetic ganglion of normal and dystrophic mdx mice: immunolocalization by electron microscopy and biochemical characterization","volume":"80","author":"De Stefano","year":"1997","journal-title":"Neuroscience"},{"key":"10.1016\/j.nbd.2022.105718_bb0305","doi-asserted-by":"crossref","first-page":"929","DOI":"10.1016\/j.nbd.2005.06.006","article-title":"Lack of dystrophin leads to the selective loss of superior cervical ganglion neurons projecting to muscular targets in genetically dystrophic mdx mice","volume":"20","author":"De Stefano","year":"2005","journal-title":"Neurobiol. Dis."},{"key":"10.1016\/j.nbd.2022.105718_bb0310","doi-asserted-by":"crossref","first-page":"54","DOI":"10.1006\/nbdi.2002.0495","article-title":"Dystrophin stabilizes alpha 3- but not alpha 7-containing nicotinic acetylcholine receptor subtypes at the postsynaptic apparatus in the mouse superior cervical ganglion","volume":"10","author":"Del Signore","year":"2002","journal-title":"Neurobiol. Dis."},{"key":"10.1016\/j.nbd.2022.105718_bb0315","doi-asserted-by":"crossref","first-page":"1769","DOI":"10.1113\/jphysiol.2008.166256","article-title":"Nitric oxide generated by muscle corrects defects in hippocampal neurogenesis and neural differentiation caused by muscular dystrophy","volume":"587","author":"Deng","year":"2009","journal-title":"J. Physiol."},{"key":"10.1016\/j.nbd.2022.105718_bb0320","doi-asserted-by":"crossref","first-page":"528","DOI":"10.1016\/j.nbd.2010.10.024","article-title":"Lack of dystrophin functionally affects \u03b13\u03b22\/\u03b24-nicotinic acethylcholine receptors in sympathetic neurons of dystrophic mdx mice","volume":"41","author":"Di Angelantonio","year":"2011","journal-title":"Neurobiol. Dis."},{"key":"10.1016\/j.nbd.2022.105718_bb0325","doi-asserted-by":"crossref","first-page":"437","DOI":"10.1016\/j.nmd.2020.05.001","article-title":"Combining genetics, neuropsychology and neuroimaging to improve understanding of brain involvement in Duchenne muscular dystrophy - a narrative review","volume":"30","author":"Doorenweerd","year":"2020","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0330","doi-asserted-by":"crossref","first-page":"403","DOI":"10.1002\/ana.24222","article-title":"Reduced cerebral gray matter and altered white matter in boys with Duchenne Muscular Dystrophy","volume":"76","author":"Doorenweerd","year":"2014","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0335","doi-asserted-by":"crossref","first-page":"12575","DOI":"10.1038\/s41598-017-12981-5","article-title":"Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy","volume":"7","author":"Doorenweerd","year":"2017","journal-title":"Sci. Rep."},{"key":"10.1016\/j.nbd.2022.105718_bb0340","doi-asserted-by":"crossref","first-page":"316","DOI":"10.1111\/j.1469-8749.1988.tb14556.x","article-title":"Language and learning disorders of older boys with Duchenne muscular dystrophy","volume":"30","author":"Dorman","year":"1988","journal-title":"Dev. Med. Child Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0345","doi-asserted-by":"crossref","first-page":"605","DOI":"10.1016\/0306-4522(96)00069-3","article-title":"Dystrophin and the dystrophin-associated glycoprotein, beta-dystroglycan, colocalize in photoreceptor synaptic complexes of the human retina","volume":"73","author":"Drenckhahn","year":"1996","journal-title":"Neuroscience"},{"key":"10.1016\/j.nbd.2022.105718_bb0350","article-title":"Duchenne muscular dystrophy","volume":"7","author":"Duan","year":"2021","journal-title":"Nat. Rev. Dis. Prim."},{"key":"10.1016\/j.nbd.2022.105718_bb0355","doi-asserted-by":"crossref","first-page":"296","DOI":"10.1136\/adc.40.211.296","article-title":"lntellectual impairment in muscular dystrophy","volume":"40","author":"Dubowitz","year":"1965","journal-title":"Arch. Dis. Child."},{"key":"10.1016\/j.nbd.2022.105718_bb0360","first-page":"1","article-title":"Muscle disorders in childhood","volume":"16","author":"Dubowitz","year":"1978","journal-title":"Major Probl. Clin. Pediatr."},{"key":"10.1016\/j.nbd.2022.105718_bb0365","doi-asserted-by":"crossref","first-page":"431","DOI":"10.1111\/j.1749-6632.1979.tb37373.x","article-title":"Involvement of the nervous system in muscular dystrophies in man","volume":"317","author":"Dubowitz","year":"1979","journal-title":"Ann. N. Y. Acad. Sci."},{"key":"10.1016\/j.nbd.2022.105718_bb0370","doi-asserted-by":"crossref","first-page":"805","DOI":"10.1093\/brain\/92.4.805","article-title":"The central nervous system in Duchenne muscular dystrophy","volume":"92","author":"Dubowitz","year":"1969","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2022.105718_bb0375","doi-asserted-by":"crossref","first-page":"1193","DOI":"10.1073\/pnas.0409308102","article-title":"Loss of perivascular aquaporin 4 may underlie deficient water and K+ homeostasis in the human epileptogenic hippocampus","volume":"102","author":"Eid","year":"2005","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.nbd.2022.105718_bb0380","series-title":"Oxford Monographs on Medical Genetics","first-page":"392","article-title":"Duchenne Muscular Dystrophy","volume":"xv","author":"Emery","year":"1993"},{"key":"10.1016\/j.nbd.2022.105718_bb0385","doi-asserted-by":"crossref","first-page":"687","DOI":"10.1016\/S0140-6736(02)07815-7","article-title":"The muscular dystrophies","volume":"359","author":"Emery","year":"2002","journal-title":"Lancet"},{"key":"10.1016\/j.nbd.2022.105718_bb0390","doi-asserted-by":"crossref","first-page":"189","DOI":"10.1111\/j.1399-0004.1976.tb00033.x","article-title":"Clinical studies in benign (Becker type) X-linked muscular dystrophy","volume":"10","author":"Emery","year":"1976","journal-title":"Clin. Genet."},{"key":"10.1016\/j.nbd.2022.105718_bb0395","doi-asserted-by":"crossref","first-page":"315","DOI":"10.1038\/345315a0","article-title":"Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle","volume":"345","author":"Ervasti","year":"1990","journal-title":"Nature"},{"key":"10.1016\/j.nbd.2022.105718_bb0400","first-page":"116","article-title":"Epilepsy in boys with Duchenne Muscular Dystrophy","volume":"3","author":"Etemadifar","year":"2004","journal-title":"J. Res. Med. Sci."},{"key":"10.1016\/j.nbd.2022.105718_bb0405","doi-asserted-by":"crossref","first-page":"559","DOI":"10.1212\/WNL.55.4.559","article-title":"Loss of Dp140 dystrophin. Isoform and intellectual impairment in Duchenne dystrophy","volume":"55","author":"Felisari","year":"2000","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2022.105718_bb0410","doi-asserted-by":"crossref","first-page":"2425","DOI":"10.1172\/JCI117250","article-title":"Retinal signal transmission in Duchenne muscular dystrophy: evidence for dysfunction in the photoreceptor\/depolarizing bipolar cell pathway","volume":"93","author":"Fitzgerald","year":"1994","journal-title":"J. Clin. Invest."},{"key":"10.1016\/j.nbd.2022.105718_bb0415","doi-asserted-by":"crossref","first-page":"597","DOI":"10.1002\/glia.20633","article-title":"Kir4.1 and AQP4 associate with Dp71- and Utrophin-DAPs complexes in specific and defined microdomains of M\u00fcller retinal glial cell membrane","volume":"56","author":"Fort","year":"2008","journal-title":"Glia"},{"key":"10.1016\/j.nbd.2022.105718_bb0420","doi-asserted-by":"crossref","first-page":"5105","DOI":"10.1523\/JNEUROSCI.4950-07.2008","article-title":"The dystrophin Dp186 isoform regulates neurotransmitter release at a central synapse in Drosophila","volume":"28","author":"Fradkin","year":"2008","journal-title":"J. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0425","doi-asserted-by":"crossref","DOI":"10.1016\/j.yexcr.2019.111715","article-title":"Cultured hippocampal neurons of dystrophic mdx mice respond differently from those of wild typw mice to an acute treatment with corticosterone","volume":"386","author":"Fragapane","year":"2020","journal-title":"Exp. Cell Res."},{"key":"10.1016\/j.nbd.2022.105718_bb0430","doi-asserted-by":"crossref","first-page":"e1762","DOI":"10.1371\/journal.pone.0001762","article-title":"L-Type Ca2+ Channel Function Is Linked to Dystrophin Expression in Mammalian Muscle","volume":"3","author":"Friedrich","year":"2008","journal-title":"PlosOne"},{"key":"10.1016\/j.nbd.2022.105718_bb0435","doi-asserted-by":"crossref","first-page":"90","DOI":"10.1096\/fj.00-0260com","article-title":"Aquaporin-4 deficiency in skeletal muscle and brain of dystrophic mdx mice","volume":"15","author":"Frigeri","year":"2001","journal-title":"FASEB J."},{"key":"10.1016\/j.nbd.2022.105718_bb0440","first-page":"1","article-title":"Epilepsy, E\/I balance and GABA(A) receptor plasticity","volume":"28","author":"Fritschy","year":"2008","journal-title":"Front. Mol. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0445","doi-asserted-by":"crossref","first-page":"10296","DOI":"10.1523\/JNEUROSCI.1823-16.2016","article-title":"Neuronal Dystroglycan Is Necessary for Formation and Maintenance of Functional CCK-Positive Basket Cell Terminals on Pyramidal Cells","volume":"36","author":"Fr\u00fch","year":"2016","journal-title":"J. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0450","doi-asserted-by":"crossref","first-page":"109","DOI":"10.1016\/j.nbd.2015.11.018","article-title":"Wnt signaling pathway improves central inhibitory synaptic transmission in a mouse model of Duchenne muscular dystrophy","volume":"86","author":"Fuenzalida","year":"2016","journal-title":"Neurobiol. Dis."},{"key":"10.1016\/j.nbd.2022.105718_bb0455","doi-asserted-by":"crossref","first-page":"79","DOI":"10.1016\/j.bbrc.2014.08.064","article-title":"Somatodendritic and excitatory postsynaptic distribution of neuron-type dystrophin isoform, Dp40, in hippocampal neurons","volume":"452","author":"Fujimoto","year":"2014","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"10.1016\/j.nbd.2022.105718_bb0460","doi-asserted-by":"crossref","first-page":"186","DOI":"10.1038\/nn1837","article-title":"Retrograde modulation of presynaptic release probability through signaling mediated by PSD-95-neuroligin","volume":"10","author":"Futai","year":"2007","journal-title":"Nat. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0465","doi-asserted-by":"crossref","first-page":"16456","DOI":"10.1073\/pnas.1910456117","article-title":"Premature termination codons in the DMD gene cause reduced local mRNA synthesis","volume":"117","author":"Garc\u00eda-Rodr\u00edguez","year":"2020","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.nbd.2022.105718_bb0470","doi-asserted-by":"crossref","first-page":"96","DOI":"10.1016\/j.brainres.2012.09.021","article-title":"Quantitative changes of nicotinic receptors in the hippocampus of dystrophin deficient mice","volume":"1483","author":"Ghedini","year":"2012","journal-title":"Brain Res."},{"key":"10.1016\/j.nbd.2022.105718_bb0475","doi-asserted-by":"crossref","first-page":"278","DOI":"10.1016\/j.gde.2011.02.001","article-title":"Dystroglycanopathies: Coming into focus","volume":"21","author":"Godfrey","year":"2011","journal-title":"Curr. Opin. Genet. Dev."},{"key":"10.1016\/j.nbd.2022.105718_bb0480","doi-asserted-by":"crossref","first-page":"287","DOI":"10.1007\/s11940-014-0287-4","article-title":"Current treatment and management of dystrophinopathies","volume":"16","author":"Goemans","year":"2014","journal-title":"Curr. Treat. Options Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0485","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1016\/S1090-3798(97)80042-6","article-title":"Epilepsy in Duchenne and Becker muscular dystrophies","volume":"4","author":"Goodwin","year":"1997","journal-title":"Eur. J. Paediatr. Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0490","doi-asserted-by":"crossref","first-page":"P134","DOI":"10.1016\/j.ejpn.2020.10.008","article-title":"Adaptive skills and mental health in children and adolescents with neuromuscular diseases","volume":"30","author":"Gosar","year":"2021","journal-title":"Eur. J. Paedr. Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0495","series-title":"Pseudo-hypertrophic muscular paralysis","author":"Gowers","year":"1879"},{"key":"10.1016\/j.nbd.2022.105718_bb0505","doi-asserted-by":"crossref","first-page":"270","DOI":"10.1038\/nm.3765","article-title":"Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomers","volume":"21","author":"Goyenvalle","year":"2015","journal-title":"Nat. Med."},{"key":"10.1016\/j.nbd.2022.105718_bb0515","doi-asserted-by":"crossref","first-page":"186","DOI":"10.1016\/S0960-8966(00)00185-1","article-title":"Cardiac abnormalities and skeletal muscle weakness in carriers of Duchenne and Becker muscular dystrophies and controls","volume":"1","author":"Grain","year":"2001","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0520","doi-asserted-by":"crossref","first-page":"281","DOI":"10.1146\/annurev-genom-090314-025003","article-title":"The pathogenesis and therapy of muscular dystrophies","volume":"16","author":"Guiraud","year":"2015","journal-title":"Annu. Rev. Genomics Hum. Genet."},{"key":"10.1016\/j.nbd.2022.105718_bb0525","doi-asserted-by":"crossref","first-page":"233","DOI":"10.1016\/0022-510X(76)90106-4","article-title":"A comparison of the fine structure of motor end-plate in Duchenne dystrophy and in human neurogenic diseases","volume":"28","author":"Harriman","year":"1976","journal-title":"J. Neurol. Sci."},{"key":"10.1016\/j.nbd.2022.105718_bb0530","doi-asserted-by":"crossref","first-page":"511","DOI":"10.1146\/annurev.neuro.22.1.511","article-title":"Central nervous system neuronal migration","volume":"22","author":"Hatten","year":"1999","journal-title":"Annu. Rev. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0535","first-page":"11","article-title":"Cerebellar synapse properties and cerebellum-dependent motor and non-motor performance in Dp71-null mice","author":"Helleringer","year":"2018","journal-title":"Dis. Model. Mech."},{"key":"10.1016\/j.nbd.2022.105718_bb0540","doi-asserted-by":"crossref","first-page":"255","DOI":"10.1016\/j.neubiorev.2015.01.023","article-title":"A possible role of dystrophin in neuronal excitability: a review of the current literature","volume":"51","author":"Hendriksen","year":"2015","journal-title":"Neurosci. Biobehav. Rev."},{"key":"10.1016\/j.nbd.2022.105718_bb0545","doi-asserted-by":"crossref","first-page":"488","DOI":"10.1016\/j.ejpn.2017.12.004","article-title":"Brain-related comorbidities in boys and men with Duchenne Muscular Dystrophy: A descriptive study","volume":"22","author":"Hendriksen","year":"2018","journal-title":"Eur. J. Peadr. Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0550","doi-asserted-by":"crossref","first-page":"470","DOI":"10.1097\/00004703-200612000-00003","article-title":"Social behavior problems in boys with Duchenne muscular dystrophy","volume":"27","author":"Hinton","year":"2006","journal-title":"J. Dev. Behav. Pediatr."},{"key":"10.1016\/j.nbd.2022.105718_bb0555","doi-asserted-by":"crossref","first-page":"339","DOI":"10.1016\/j.pediatrneurol.2009.05.011","article-title":"Association of autistic spectrum disorders with dystrophinopathies","volume":"41","author":"Hinton","year":"2009","journal-title":"Pediatr. Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0560","doi-asserted-by":"crossref","first-page":"607","DOI":"10.1016\/j.neuroscience.2006.04.043","article-title":"Effect of \u03b2-dystroglycan processing on utrophin\/Dp116 anchorage in normal and mdx mouse Schwann cell membrane","volume":"141","author":"Hnia","year":"2006","journal-title":"Neuroscience"},{"key":"10.1016\/j.nbd.2022.105718_bb0565","doi-asserted-by":"crossref","first-page":"919","DOI":"10.1016\/0092-8674(87)90579-4","article-title":"Dystrophin: the protein product of the Duchenne muscular dystrophy locus","volume":"51","author":"Hoffman","year":"1987","journal-title":"Cell"},{"key":"10.1016\/j.nbd.2022.105718_bb0570","doi-asserted-by":"crossref","first-page":"105","DOI":"10.1016\/0304-3940(92)90309-U","article-title":"Localization of dystrophin in the Purkinje cells of normal mice","volume":"137","author":"Huard","year":"1992","journal-title":"Neurosci. Lett."},{"key":"10.1016\/j.nbd.2022.105718_bb0575","doi-asserted-by":"crossref","DOI":"10.1016\/j.pharmthera.2020.107719","article-title":"Current and emerging therapies for Duchenne muscular dystrophy and spinal muscular atrophy","volume":"220","author":"Iftikhar","year":"2021","journal-title":"Pharmacol. Therap."},{"key":"10.1016\/j.nbd.2022.105718_bb0580","doi-asserted-by":"crossref","first-page":"1149","DOI":"10.1093\/hmg\/5.8.1149","article-title":"Differential expression of dystrophin isoforms in strains of i mice with different mutations","volume":"5","author":"Im","year":"1996","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.nbd.2022.105718_bb0585","doi-asserted-by":"crossref","first-page":"3091","DOI":"10.1093\/hmg\/9.20.3091","article-title":"A sarcoglycan-dystroglycam complex anchors Dp116 and utrophin in the peripheral nervous system","volume":"9","author":"Imamura","year":"2000","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.nbd.2022.105718_bb0590","doi-asserted-by":"crossref","first-page":"572","DOI":"10.1016\/j.nmd.2018.04.005","article-title":"Female dystrophinopathy: review of current literature","volume":"28","author":"Ishizaki","year":"2018","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0595","doi-asserted-by":"crossref","first-page":"87","DOI":"10.1016\/0887-8994(88)90047-1","article-title":"Brain morphology in Duchenne muscular dystrophy: a Golgi study","volume":"4","author":"Jagadha","year":"1988","journal-title":"Pediatr. Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0600","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1167\/iovs.05-0597","article-title":"Identification of a beta-dystroglycan immunoreactive subcompartment in photoreceptor terminals","volume":"47","author":"Jastrow","year":"2006","journal-title":"Invest. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.nbd.2022.105718_bb0605","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1016\/0960-8966(91)90001-9","article-title":"Diagnostic criteria for Duchenne and Becker muscular dystrophy and myotonic dystrophy","volume":"1","author":"Jennekens","year":"1991","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0610","doi-asserted-by":"crossref","first-page":"123","DOI":"10.1093\/brain\/97.1.123","article-title":"Duchenne dystrophy: II. Morphometric study of motor end-plate fine structure","volume":"97","author":"Jerusalem","year":"1974","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2022.105718_bb0615","doi-asserted-by":"crossref","first-page":"515","DOI":"10.1016\/0960-8966(93)90107-U","article-title":"Characterization and subcellular localization of the dystrophin-protein 71 (Dp71) from brain","volume":"3","author":"Jung","year":"1993","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0620","doi-asserted-by":"crossref","first-page":"435","DOI":"10.1111\/j.1469-8749.1978.tb15244.x","article-title":"Early verbal disability in children with Duchenne muscular dystrophy","volume":"29","author":"Karagan","year":"1978","journal-title":"Dev. Med. Child Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0625","doi-asserted-by":"crossref","first-page":"419","DOI":"10.1097\/00005053-198007000-00005","article-title":"Analysis of verbal disability in Duchenne muscular dystrophy","volume":"168","author":"Karagan","year":"1980","journal-title":"J. Nerv. Ment. Dis."},{"key":"10.1016\/j.nbd.2022.105718_bb0635","doi-asserted-by":"crossref","first-page":"1435","DOI":"10.1097\/00001756-199704140-00022","article-title":"Increased cerebral choline-compounds in Duchenne muscular dystrophy","volume":"8","author":"Kato","year":"1997","journal-title":"Neuroreport"},{"key":"10.1016\/j.nbd.2022.105718_bb0640","doi-asserted-by":"crossref","first-page":"147","DOI":"10.1002\/humu.10310","article-title":"Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation","volume":"23","author":"Kato","year":"2004","journal-title":"Hum. Mutat."},{"issue":"ra56","key":"10.1016\/j.nbd.2022.105718_bb0645","article-title":"Microtubules underlie Dys function in Duchenne muscular dystrophy","volume":"5","author":"Khairallah","year":"2012","journal-title":"Sci. Signal."},{"key":"10.1016\/j.nbd.2022.105718_bb0650","doi-asserted-by":"crossref","first-page":"443","DOI":"10.1016\/j.rehab.2013.06.002","article-title":"Evolution of life expectancy of patients with Duchenne muscular dystrophy at AFM Yolaine de Kepper centre between 1981 and 2011","volume":"56","author":"Kieny","year":"2013","journal-title":"Ann. Phys. Rehabil. Med."},{"key":"10.1016\/j.nbd.2022.105718_bb0655","doi-asserted-by":"crossref","first-page":"11642","DOI":"10.1073\/pnas.89.23.11642","article-title":"Detection of dystrophin in the postsynaptic density of rat brain and deficiency in a mouse model of Duchenne muscular dystrophy","volume":"89","author":"Kim","year":"1992","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.nbd.2022.105718_bb0660","doi-asserted-by":"crossref","first-page":"446","DOI":"10.1002\/ana.410380315","article-title":"Deficiency of brain synaptic dystrophin in human Duchenne muscular dystrophy","volume":"38","author":"Kim","year":"1995","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0665","doi-asserted-by":"crossref","first-page":"4457","DOI":"10.1046\/j.1460-9568.1999.00887.x","article-title":"Altered synaptic clustering of GABAA receptors in mice lacking dystrophin (i mice)","volume":"11","author":"Knuesel","year":"1999","journal-title":"Eur. J. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0670","doi-asserted-by":"crossref","first-page":"1113","DOI":"10.1046\/j.0953-816x.2001.01476.x","article-title":"Alterations in dystrophin and utrophin expression parallel the reorganization of GABAergic synapses in a mouse model of temporal lobe epilepsy","volume":"13","author":"Knuesel","year":"2001","journal-title":"Eur. J. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0675","doi-asserted-by":"crossref","first-page":"509","DOI":"10.1016\/0092-8674(87)90504-6","article-title":"Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals","volume":"50","author":"Koenig","year":"1987","journal-title":"Cell"},{"key":"10.1016\/j.nbd.2022.105718_bb0680","doi-asserted-by":"crossref","first-page":"219","DOI":"10.1016\/0092-8674(88)90383-2","article-title":"The complete sequence of dystrophin predicts a rodshaped cytoskeletal protein","volume":"53","author":"Koenig","year":"1988","journal-title":"Cell"},{"key":"10.1016\/j.nbd.2022.105718_bb0685","doi-asserted-by":"crossref","first-page":"298","DOI":"10.1016\/S0006-8993(99)01737-0","article-title":"Dystrophin is required for organizing large acetylcholine receptor aggregates","volume":"839","author":"Kong","year":"1999","journal-title":"Brain Res."},{"key":"10.1016\/j.nbd.2022.105718_bb0690","doi-asserted-by":"crossref","first-page":"735","DOI":"10.1002\/(SICI)1097-4547(19980315)51:6<735::AID-JNR7>3.0.CO;2-C","article-title":"Differential distribution of beta dystroglycan in rabbit and rat retina","volume":"51","author":"Koulen","year":"1998","journal-title":"J. Neurosci. Res."},{"key":"10.1016\/j.nbd.2022.105718_bb0695","doi-asserted-by":"crossref","first-page":"209","DOI":"10.1016\/0022-510X(71)90090-6","article-title":"Mental retardation in patients with Duchenne progressive muscular dystrophy","volume":"14","author":"Kozicka","year":"1971","journal-title":"J. Neurol. Sci."},{"key":"10.1016\/j.nbd.2022.105718_bb0700","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0108364","article-title":"Aberrant location of inhibitory synaptic marker proteins in the hippocampus of dystrophin-deficient mice: implications for cognitive impairment in Duchenne Muscular Dystrophy","volume":"9","author":"Krasowska","year":"2014","journal-title":"PLoS One"},{"key":"10.1016\/j.nbd.2022.105718_bb0705","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1111\/j.1440-1681.2007.04816.x","article-title":"GABAA receptor expression and inhibitory post-synaptic inhibitory currents in cerebellar Purkinje cells in dystrophin deficient mdx mice","volume":"35","author":"Kueh","year":"2008","journal-title":"Clin. Exp. Pharmacol. Physiol."},{"key":"10.1016\/j.nbd.2022.105718_bb0710","doi-asserted-by":"crossref","first-page":"558","DOI":"10.1016\/j.nbd.2011.05.002","article-title":"Reduced postsynaptic GABAA receptor number and enhanced gaboxadol induced change in holding currents in Purkinje cells of the dystrophin-deficient mdx mouse","volume":"43","author":"Kueh","year":"2011","journal-title":"Neurobiol. Dis."},{"key":"10.1016\/j.nbd.2022.105718_bb0715","doi-asserted-by":"crossref","first-page":"5346","DOI":"10.1073\/pnas.89.12.5346","article-title":"A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues","volume":"89","author":"Lederfein","year":"1992","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.nbd.2022.105718_bb0720","doi-asserted-by":"crossref","first-page":"577","DOI":"10.1111\/j.1469-8749.1981.tb02039.x","article-title":"Intellect and behaviour in Duchenne muscular dystrophy","volume":"23","author":"Leibowitz","year":"1981","journal-title":"Dev. Med. Child Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0725","doi-asserted-by":"crossref","first-page":"1877","DOI":"10.1093\/hmg\/2.11.1877","article-title":"A point mutation at the carboxy terminus of the human dystrophin gene: implication for an association with mental retardation in DMD patients","volume":"2","author":"Lenk","year":"1993","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.nbd.2022.105718_bb0730","doi-asserted-by":"crossref","first-page":"535","DOI":"10.1007\/s00232-018-0036-9","article-title":"Biochemical and functional interplay between ion channels and the components of the dystrophin-associated glycoprotein complex","volume":"251","author":"Leyva-Leyva","year":"2018","journal-title":"J. Membr. Biol."},{"key":"10.1016\/j.nbd.2022.105718_bb0735","doi-asserted-by":"crossref","first-page":"691","DOI":"10.1111\/j.1460-9568.2011.07984.x","article-title":"Lack of dystrophin in mdx mice modulates the expression of genes involved in neuron survival and differentiation","volume":"35","author":"Licursi","year":"2012","journal-title":"Eur. J. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0740","first-page":"1543","article-title":"Dystrophin and Dp140 in the adult rodent kidney","volume":"78","author":"Lidov","year":"1998","journal-title":"Lab. Investig."},{"key":"10.1016\/j.nbd.2022.105718_bb0745","doi-asserted-by":"crossref","first-page":"725","DOI":"10.1038\/348725a0","article-title":"Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons","volume":"348","author":"Lidov","year":"1990","journal-title":"Nature"},{"key":"10.1016\/j.nbd.2022.105718_bb0750","doi-asserted-by":"crossref","first-page":"167","DOI":"10.1016\/0306-4522(93)90392-S","article-title":"The distribution of dystrophin in the murine central nervous system: an immunocytochemical study","volume":"54","author":"Lidov","year":"1993","journal-title":"Neuroscience"},{"key":"10.1016\/j.nbd.2022.105718_bb0755","doi-asserted-by":"crossref","first-page":"329","DOI":"10.1093\/hmg\/4.3.329","article-title":"Dp140: a novel 140 kDa CNS transcript from the dystrophin locus","volume":"4","author":"Lidov","year":"1995","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.nbd.2022.105718_bb0760","doi-asserted-by":"crossref","first-page":"765","DOI":"10.3390\/genes11070765","article-title":"Cardiac involvement in dystrophin-deficient females: current understanding and implications for the treatment of dystrophinopathies","volume":"11","author":"Lim","year":"2020","journal-title":"Genes"},{"key":"10.1016\/j.nbd.2022.105718_bb0765","doi-asserted-by":"crossref","first-page":"402","DOI":"10.1016\/j.nbd.2008.07.021","article-title":"Components of the NGF signaling complex are altered in mdx mouse superior cervical ganglion and its target organs","volume":"32","author":"Lombardi","year":"2008","journal-title":"Neurobiol. Dis."},{"key":"10.1016\/j.nbd.2022.105718_bb0770","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.mcn.2017.01.006","article-title":"NGF-dependent axon growth and regeneration are altered in sympathetic neurons of dystrophic mdx mice","volume":"80","author":"Lombardi","year":"2017","journal-title":"Mol. Cell. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0775","doi-asserted-by":"crossref","first-page":"603","DOI":"10.1007\/s12035-016-0311-7","article-title":"Dysregulation of intracellular Ca2+ in dystrophic cortical and hippocampal neurons","volume":"55","author":"Lopez","year":"2018","journal-title":"Mol. Neurobiol."},{"key":"10.1016\/j.nbd.2022.105718_bb0780","doi-asserted-by":"crossref","first-page":"969","DOI":"10.1007\/BF01187915","article-title":"Structure and function of the neuromuscular junction in young adult mdx mice","volume":"20","author":"Lyons","year":"1991","journal-title":"J. Neurocytol."},{"key":"10.1016\/j.nbd.2022.105718_bb0785","article-title":"Schwann cell-specific Dp116 is expressed in glioblastoma cells, revealing two novel DMD gene splicing patterns","volume":"20","author":"Mahyoob Rani","year":"2019","journal-title":"Byochem. Byophis. Rep."},{"key":"10.1016\/j.nbd.2022.105718_bb0790","doi-asserted-by":"crossref","first-page":"118","DOI":"10.1136\/adc.49.2.118","article-title":"Evidence for early impairment of verbal intelligence in Duchenne muscular dystrophy","volume":"49","author":"Marsh","year":"1974","journal-title":"Arch. Dis. Child."},{"key":"10.1016\/j.nbd.2022.105718_bb0795","doi-asserted-by":"crossref","first-page":"251","DOI":"10.3390\/genes8100251","article-title":"Dystrophin Dp116: a yet to be investigated product of the Duchenne muscular dystrophy gene","volume":"8","author":"Matsuo","year":"2017","journal-title":"Genes"},{"key":"10.1016\/j.nbd.2022.105718_bb0800","doi-asserted-by":"crossref","first-page":"918","DOI":"10.1124\/mol.108.052274","article-title":"Acetylcholine-stimulated [3H]GABA release from mouse brain synaptosomes is modulated by alpha4beta2 and alpha4alpha5beta2 nicotinic receptor subtypes","volume":"75","author":"McClure-Begley","year":"2009","journal-title":"Mol. Pharmacol."},{"key":"10.1016\/j.nbd.2022.105718_bb0805","doi-asserted-by":"crossref","first-page":"277","DOI":"10.1016\/S0165-0173(99)00090-9","article-title":"Brain dystrophin, neurogenetics and mental retardation","volume":"32","author":"Mehler","year":"2000","journal-title":"Brain Res. Rev."},{"key":"10.1016\/j.nbd.2022.105718_bib1381","doi-asserted-by":"crossref","first-page":"2461","DOI":"10.1073\/pnas.89.6.2461","article-title":"Enhanced sensitivity of hippocampal pyramidal neurons from mdx mice to hypoxia-induced loss of synaptic transmission","volume":"89","author":"Mehler","year":"1992","journal-title":"Proc. Nati. Acad. Sci. USA"},{"key":"10.1016\/j.nbd.2022.105718_bb0810","first-page":"143","article-title":"Neural progenitor cells and developmental disorders. Mental retardation and developmental disabilities","volume":"4","author":"Mehler","year":"1998","journal-title":"Res. Rev."},{"key":"10.1016\/j.nbd.2022.105718_bb0815","doi-asserted-by":"crossref","first-page":"711","DOI":"10.1192\/bjp.162.5.711b","article-title":"Association of schizophrenia and Duchenne muscular dystrophy","volume":"162","author":"Melo","year":"1993","journal-title":"Br. J. Psychiatry"},{"key":"10.1016\/j.nbd.2022.105718_bb0820","doi-asserted-by":"crossref","first-page":"304","DOI":"10.1002\/ana.23528","article-title":"Evidence-based path to newborn screening for Duchenne muscular dystrophy","volume":"71","author":"Mendell","year":"2012","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0825","doi-asserted-by":"crossref","first-page":"2025","DOI":"10.1016\/S0140-6736(19)32910-1","article-title":"Muscular dystrophies","volume":"394","author":"Mercuri","year":"2019","journal-title":"Lancet"},{"key":"10.1016\/j.nbd.2022.105718_bb0830","doi-asserted-by":"crossref","first-page":"442","DOI":"10.1038\/nm1736","article-title":"Genetic and pharmacologic inhibition of mitochondrial-dependent necrosis attenuates muscular dystrophy","volume":"14","author":"Millay","year":"2008","journal-title":"Nat. Med."},{"key":"10.1016\/j.nbd.2022.105718_bb0835","doi-asserted-by":"crossref","first-page":"561","DOI":"10.1002\/mus.10416","article-title":"Acetylcholine receptor distribution and synapse elimination at the developing neuromuscular junction of mdx mice","volume":"28","author":"Minatel","year":"2003","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.nbd.2022.105718_bb0840","series-title":"Reorganization of inhibitory synapses and increased PSD length of perforated excitatory synapses in hippocampal area CA1 of dystrophin-deficient mdx mice cerebral cortex","first-page":"876","volume":"19","author":"Miranda","year":"2009"},{"key":"10.1016\/j.nbd.2022.105718_bb0845","doi-asserted-by":"crossref","first-page":"134","DOI":"10.1016\/j.nbd.2011.02.017","article-title":"Altered presynaptic ultrastructure in excitatory hippocampal synapses of mice lacking dystrophins Dp427 or Dp71","volume":"43","author":"Miranda","year":"2011","journal-title":"Neurobiol. Dis."},{"key":"10.1016\/j.nbd.2022.105718_bb0850","doi-asserted-by":"crossref","first-page":"60","DOI":"10.1186\/s13229-015-0053-9","article-title":"Altered social behavior and ultrasonic communication in the dystrophin deficient mdx mouse model of Duchenne muscular dystrophy","volume":"6","author":"Miranda","year":"2015","journal-title":"Mol. Autism"},{"key":"10.1016\/j.nbd.2022.105718_bb0855","doi-asserted-by":"crossref","first-page":"775","DOI":"10.1016\/j.nmd.2016.08.006","article-title":"Reduced neuronal density in the CA1 anterodorsal hippocampus of the mdx mouse","volume":"26","author":"Miranda","year":"2016","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0860","doi-asserted-by":"crossref","first-page":"361","DOI":"10.1006\/bbrc.1995.2474","article-title":"Apodystrophins (Dp140 and Dp71)and dystrophin splicing isoforms in developing brain","volume":"215","author":"Morris","year":"1995","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"10.1016\/j.nbd.2022.105718_bb0865","first-page":"70","article-title":"The psychosocial factors in muscular dystrophy","volume":"3","author":"Morrow","year":"1954","journal-title":"J. Child Psychol. Psychiatry"},{"key":"10.1016\/j.nbd.2022.105718_bb0870","doi-asserted-by":"crossref","first-page":"731","DOI":"10.1016\/S1474-4422(03)00585-4","article-title":"Dystrophin and mutations: one gene, several proteins, multiple phenotypes","volume":"2","author":"Muntoni","year":"2003","journal-title":"Lancet Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb0875","series-title":"Muscle. Proceedings of symposium at faculty of Medicine","first-page":"529","article-title":"Varying manifestations of Duchenne muscular dystrophy in a family with affected females","author":"Murphy","year":"1964"},{"key":"10.1016\/j.nbd.2022.105718_bb0880","doi-asserted-by":"crossref","first-page":"742","DOI":"10.1002\/mus.880130813","article-title":"Neuromuscular transmission in the mdx mouse","volume":"13","author":"Nagel","year":"1990","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.nbd.2022.105718_bb0885","doi-asserted-by":"crossref","first-page":"47","DOI":"10.1002\/(SICI)1098-1136(199903)26:1<47::AID-GLIA5>3.0.CO;2-5","article-title":"Immunogold evidence suggests that coupling of K1 siphoning and water transport in rat retinal Muller cells is mediated by a coenrichment of Kir4.1 and AQP4 in specific membrane domains","volume":"26","author":"Nagelhus","year":"1999","journal-title":"Glia"},{"key":"10.1016\/j.nbd.2022.105718_bb0890","doi-asserted-by":"crossref","first-page":"1748","DOI":"10.1007\/s12035-019-01845-w","article-title":"Dystrophin Dp71 and the neuropathophysiology of Duchenne muscular dystrophy","volume":"57","author":"Naidoo","year":"2020","journal-title":"Mol. Neurobiol."},{"key":"10.1016\/j.nbd.2022.105718_bb0895","doi-asserted-by":"crossref","first-page":"303","DOI":"10.3390\/ph8020303","article-title":"X-Linked Dilated Cardiomyopathy: A Cardiospecific Phenotype of Dystrophinopathy","volume":"8","author":"Nakamura","year":"2015","journal-title":"Pharmaceuticals"},{"key":"10.1016\/j.nbd.2022.105718_bb0900","doi-asserted-by":"crossref","first-page":"6","DOI":"10.2223\/JPED.2148","article-title":"Mental retardation in Duchenne muscular dystrophy","volume":"88","author":"Nardes","year":"2012","journal-title":"J. Pediatr."},{"key":"10.1016\/j.nbd.2022.105718_bb0905","doi-asserted-by":"crossref","DOI":"10.1016\/j.ebiom.2020.103032","article-title":"Recent insights into neuromuscular junction biology in Duchenne muscular dystrophy: Impacts, challenges, and opportunities","volume":"61","author":"Ng","year":"2020","journal-title":"EBioMedicine"},{"key":"10.1016\/j.nbd.2022.105718_bb0910","doi-asserted-by":"crossref","first-page":"935","DOI":"10.1016\/j.neuroscience.2004.07.055","article-title":"The role of aquaporin-4 in the blood\u2013brain barrier development and integrity: studies in animal and cell culture models","volume":"129","author":"Nicchia","year":"2004","journal-title":"Neuroscience"},{"key":"10.1016\/j.nbd.2022.105718_bb0915","doi-asserted-by":"crossref","DOI":"10.1007\/s00424-021-02623-1","article-title":"Complexity of skeletal muscle degeneration: multi-systemspatho physiology and organ crosstalk in dystrophinopathy","author":"Ohlendieck","year":"2021","journal-title":"Pflugers Arch."},{"key":"10.1016\/j.nbd.2022.105718_bb0920","doi-asserted-by":"crossref","first-page":"6126","DOI":"10.1523\/JNEUROSCI.0322-12.2012","article-title":"Presynaptic dystroglycan-pikachurin complex regulates the proper synaptic connection between retinal photoreceptor and bipolar cells","volume":"32","author":"Omori","year":"2012","journal-title":"J. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0925","doi-asserted-by":"crossref","first-page":"6126","DOI":"10.1523\/JNEUROSCI.0322-12.2012","article-title":"Presynaptic dystroglycan-pikachurin complex regulates the proper synaptic connection between retinal photoreceptor and bipolar cells","volume":"32","author":"Omori","year":"2012","journal-title":"J. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0930","doi-asserted-by":"crossref","first-page":"705","DOI":"10.1016\/j.jpeds.2012.03.020","article-title":"Attention deficit hyperactivity disorder and cognitive function in Duchenne muscular dystrophy: phenotype-genotype correlation","volume":"161","author":"Pane","year":"2012","journal-title":"J. Pediatr."},{"key":"10.1016\/j.nbd.2022.105718_bb0935","doi-asserted-by":"crossref","first-page":"451","DOI":"10.1016\/j.nmd.2013.02.012","article-title":"Early neurodevelopmental assessment in Duchenne muscular dystrophy","volume":"23","author":"Pane","year":"2013","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0940","doi-asserted-by":"crossref","first-page":"233","DOI":"10.23736\/S0026-4946.16.04380-2","article-title":"Autism spectrum disorders in children affected by Duchenne muscular dystrophy","volume":"70","author":"Parisi","year":"2018","journal-title":"Minerva Pediatr."},{"key":"10.1016\/j.nbd.2022.105718_bb0945","doi-asserted-by":"crossref","first-page":"462","DOI":"10.1016\/j.nmd.2021.02.004","article-title":"Third case of Duchenne muscular dystrophy and West syndrome: Expanding the spectrum of the DMD neuropsychiatric phenotype","volume":"31","author":"Pe\u00f1a-Padilla","year":"2021","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb0950","doi-asserted-by":"crossref","first-page":"105","DOI":"10.1016\/j.neuint.2018.06.001","article-title":"Altered release and uptake of gamma-aminobutyric acid in the cerebellum of dystrophin-deficient mice","volume":"118","author":"Pereira da Silva","year":"2018","journal-title":"Neurochem. Int."},{"key":"10.1016\/j.nbd.2022.105718_bb0955","first-page":"849426","article-title":"Dystrophins, utrophins, and associated scaffolding complexes: role in mammalian brain and implications for therapeutic strategies","volume":"2010","author":"Perronnet","year":"2010","journal-title":"J. Biomed. Biotechnol."},{"key":"10.1016\/j.nbd.2022.105718_bb0960","doi-asserted-by":"crossref","first-page":"760","DOI":"10.3389\/fnins.2020.00760","article-title":"Dystrophin is required for the proper timing in retinal histogenesis: a thorough investigation on the mdx mouse model of Duchenne muscular dystrophy","volume":"14","author":"Persiconi","year":"2020","journal-title":"Front. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb0965","first-page":"55","article-title":"Developmental lag of visuospatial attention in Duchenne muscular dystrophy","volume":"14","author":"Piccini","year":"2014","journal-title":"Res. Dev. Disabil."},{"key":"10.1016\/j.nbd.2022.105718_bb0970","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/s12035-009-8089-5","article-title":"The Roles of the Dystrophin-associated glycoprotein complex at the synapse","volume":"41","author":"Pilgram","year":"2010","journal-title":"Mol. Neurobiol."},{"key":"10.1016\/j.nbd.2022.105718_bb0975","doi-asserted-by":"crossref","first-page":"252","DOI":"10.3389\/fphys.2015.00252","article-title":"Pre- and postsynaptic changes in the neuromuscualr junction in dystrophic mice","volume":"6","author":"Pratt","year":"2015","journal-title":"Front. Physiol."},{"key":"10.1016\/j.nbd.2022.105718_bb0980","doi-asserted-by":"crossref","first-page":"1271","DOI":"10.3174\/ajnr.A6604","article-title":"In vivo evaluation of white matter abnormalities in children with Duchenne muscular dystrophy using DTI","volume":"41","author":"Preethish-Kumar","year":"2020","journal-title":"AJNR Am. J. Neuroradiol."},{"key":"10.1016\/j.nbd.2022.105718_bb0985","doi-asserted-by":"crossref","first-page":"6810","DOI":"10.1073\/pnas.1321774111","article-title":"Dystroglycan mediates homeostatic synaptic plasticity at GABAergic synapses","volume":"111","author":"Pribiag","year":"2014","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.nbd.2022.105718_bb0990","doi-asserted-by":"crossref","first-page":"363","DOI":"10.1083\/jcb.200905048","article-title":"Dystrophin is a microtubule-associated protein","volume":"186","author":"Prins","year":"2009","journal-title":"J. Cell Biol."},{"key":"10.1016\/j.nbd.2022.105718_bb0995","doi-asserted-by":"crossref","first-page":"221","DOI":"10.1136\/adc.44.234.221","article-title":"Intelligence and the gene for Duchenne muscular dystrophy","volume":"44","author":"Prosser","year":"1969","journal-title":"Arch. Dis. Child."},{"key":"10.1016\/j.nbd.2022.105718_bb1000","doi-asserted-by":"crossref","first-page":"1440","DOI":"10.1126\/science.1202768","article-title":"X-ROS signaling: rapid mechano-chemo transduction in heart","volume":"333","author":"Prosser","year":"2011","journal-title":"Science"},{"key":"10.1016\/j.nbd.2022.105718_bb1005","doi-asserted-by":"crossref","first-page":"1304","DOI":"10.1152\/jn.00248.2016","article-title":"Cognitive dysfunction in Duchenne muscular dystrophy: a possible role for neuromodulatory immune molecules","volume":"116","author":"Rae","year":"2016","journal-title":"J. Neurophysiol."},{"key":"10.1016\/j.nbd.2022.105718_bb1010","doi-asserted-by":"crossref","first-page":"148","DOI":"10.1016\/S0022-510X(98)00190-7","article-title":"Brain biochemistry in Duchenne muscular dystrophy; a 1H magnetic resonance and neuropsychological study","volume":"160","author":"Rae","year":"1998","journal-title":"J. Neurol. Sci."},{"key":"10.1016\/j.nbd.2022.105718_bb1015","doi-asserted-by":"crossref","first-page":"121","DOI":"10.1016\/S0960-8966(01)00253-X","article-title":"Abnormalities in brain biochemistry associated with lack of dystrophin: studies of the mdx mouse","volume":"12","author":"Rae","year":"2002","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb1020","doi-asserted-by":"crossref","first-page":"102700","DOI":"10.1016\/j.ebiom.2020.102700","article-title":"Social stress is lethal in the mdx model of Duchenne muscular dystrophy","volume":"55","author":"Razzoli","year":"2020","journal-title":"EBioMedicine"},{"key":"10.1016\/j.nbd.2022.105718_bb1025","doi-asserted-by":"crossref","first-page":"492","DOI":"10.1002\/phar.1909","article-title":"Advances in the Treatment of Duchenne Muscular Dystrophy: New and Emerging Pharmacotherapies","volume":"37","author":"Reinig","year":"2017","journal-title":"Pharmacotherapy"},{"key":"10.1016\/j.nbd.2022.105718_bb1030","doi-asserted-by":"crossref","first-page":"932","DOI":"10.1016\/j.nmd.2015.10.007","article-title":"Challenges of clinical trial design for DMD","volume":"12","author":"Ricotti","year":"2015","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb1035","doi-asserted-by":"crossref","first-page":"77","DOI":"10.1111\/dmcn.12922","article-title":"Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations","volume":"58","author":"Ricotti","year":"2016","journal-title":"Dev. Med. Child Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb1040","doi-asserted-by":"crossref","first-page":"896","DOI":"10.1016\/S0022-3476(76)81143-2","article-title":"Mental retardation in Duchenne Muscular dystrophy: its relation to the maternal carrier state","volume":"188","author":"Robinow","year":"1976","journal-title":"J. Pediatr."},{"key":"10.1016\/j.nbd.2022.105718_bb1045","doi-asserted-by":"crossref","DOI":"10.1016\/j.neulet.2020.135247","article-title":"Characterization of the expression of dystrophins and dystrophin associated proteins during embryonic neural stem\/progenitor cell differentiation","volume":"736","author":"Romo-Y\u00e1\u00f1ez","year":"2020","journal-title":"Neurosci. Lett."},{"key":"10.1016\/j.nbd.2022.105718_bb1050","doi-asserted-by":"crossref","first-page":"769","DOI":"10.1093\/brain\/89.4.769","article-title":"Mental deficiency associated with muscular dystrophy: A neuropathological study","volume":"89","author":"Rosman","year":"1966","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2022.105718_bb1055","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1080\/19336950.2016.1228498","article-title":"Decreased inward rectifier potassium current IK1 in dystrophin-deficient ventricular cardiomyocytes","volume":"11","author":"Rubi","year":"2017","journal-title":"Channels (Austin, Tex.)"},{"key":"10.1016\/j.nbd.2022.105718_bb1060","doi-asserted-by":"crossref","first-page":"79","DOI":"10.1186\/s13023-017-0631-3","article-title":"The burden, epidemiology, costs and treatment for Duchenne muscular dystrophy: an evidence review","volume":"12","author":"Ryder","year":"2017","journal-title":"Orphanet J. Rare Dis."},{"key":"10.1016\/j.nbd.2022.105718_bb1065","doi-asserted-by":"crossref","first-page":"36248","DOI":"10.1074\/jbc.M109.012872","article-title":"Regulation of TRPC1 and TRPC4 cation channels requires an alpha1-syntrophin-dependent complex in skeletal mouse myotubes","volume":"284","author":"Sabourin","year":"2009","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.nbd.2022.105718_bb1070","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1111\/j.1750-3639.1996.tb00780.x","article-title":"Dystrophin and its isoforms","volume":"6","author":"Sadoulet-Puccio","year":"1996","journal-title":"Brain Pathol."},{"key":"10.1016\/j.nbd.2022.105718_bb1075","doi-asserted-by":"crossref","first-page":"741","DOI":"10.1212\/WNL.27.8.741","article-title":"Duchenne dystrophy: ultrastructural localization of the acetylcholine receptor and intracellular microelectrode studies of neuromuscular transmission","volume":"27","author":"Sakakibara","year":"1977","journal-title":"Neurology"},{"key":"10.1016\/j.nbd.2022.105718_bb1080","doi-asserted-by":"crossref","first-page":"382","DOI":"10.1016\/j.nmd.2008.02.004","article-title":"Regions downstream from the WW domain of dystrophin are important for binding to postsynaptic densities in the brain","volume":"18","author":"Sakamoto","year":"2008","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb1085","doi-asserted-by":"crossref","first-page":"13818","DOI":"10.1073\/pnas.250379497","article-title":"Functional muscle ischemia in neuronal nitric oxide synthase-deficient skeletal muscle of children with Duchenne muscular dystrophy","volume":"97","author":"Sander","year":"2000","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.nbd.2022.105718_bb1090","doi-asserted-by":"crossref","first-page":"dmm049028","DOI":"10.1242\/dmm.049028","article-title":"Emotional behavior and brain anatomy of the mdx52 mouse model of Duchenne muscular dystrophy","volume":"14","author":"Saoudi","year":"2021","journal-title":"Dis. Model. Mech."},{"key":"10.1016\/j.nbd.2022.105718_bb1095","doi-asserted-by":"crossref","first-page":"923","DOI":"10.1038\/nn.2160","article-title":"Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation","volume":"11","author":"Sato","year":"2008","journal-title":"Nat. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb1100","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1016\/0304-3940(95)12079-J","article-title":"Architectural changes of the cortico-spinal system in the dystrophin defective mdx mouse","volume":"200","author":"Sbriccoli","year":"1995","journal-title":"Neurosci. Lett."},{"key":"10.1016\/j.nbd.2022.105718_bb1105","doi-asserted-by":"crossref","first-page":"249","DOI":"10.1007\/s004180050165","article-title":"Localization of dystrophin and beta dystroglycan in bovine retinal photoreceptor processes extending into the postsynaptic dendritic complex","volume":"108","author":"Schmitz","year":"1997","journal-title":"Histochem. Cell Biol."},{"key":"10.1016\/j.nbd.2022.105718_bb1110","first-page":"119","article-title":"Emotional reactions in muscular dystrophy","volume":"34","author":"Schoelly","year":"1955","journal-title":"Am. J. Phys. Med."},{"key":"10.1016\/j.nbd.2022.105718_bb1115","doi-asserted-by":"crossref","first-page":"124","DOI":"10.1093\/brain\/awn253","article-title":"A deficit of brain dystrophin impairs specific amygdala GABAergic transmission and enhances defensive behaviour in mice","volume":"132","author":"Sekiguchi","year":"2009","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2022.105718_bb1120","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1016\/0304-3940(96)12747-6","article-title":"Spatial learning and hippocampal long-term potentiation are not impaired in mdx mice","volume":"211","author":"Sesay","year":"1996","journal-title":"Neurosci. Lett."},{"key":"10.1016\/j.nbd.2022.105718_bb1125","doi-asserted-by":"crossref","first-page":"2083","DOI":"10.1016\/j.yexcr.2006.03.011","article-title":"Zeta-sarcoglycan is a functional homologue of gamma-sarcoglycan in the formation of the sarcoglycan complex","volume":"312","author":"Shiga","year":"2006","journal-title":"Exp. Cell Res."},{"key":"10.1016\/j.nbd.2022.105718_bb1130","doi-asserted-by":"crossref","first-page":"743","DOI":"10.1016\/j.neubiorev.2013.03.016","article-title":"Neuropsychological and neurobehavioral functioning in Duchenne muscular dystrophy: a review","volume":"37","author":"Snow","year":"2013","journal-title":"Neurosci. Biobehav. Rev."},{"key":"10.1016\/j.nbd.2022.105718_bb1135","doi-asserted-by":"crossref","first-page":"486","DOI":"10.1080\/01688638508401280","article-title":"Neuropsychological impairment in Duchenne muscular dystrophy","volume":"7","author":"Sollee","year":"1985","journal-title":"J. Clin. Exp. Neuropsychol."},{"key":"10.1016\/j.nbd.2022.105718_bb1140","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1085\/jgp.93.1.101","article-title":"B-wave of the electroretinogram. A reflection of ON bipolar cell activity","volume":"93","author":"Stockton","year":"1989","journal-title":"J. Gen. Physiol."},{"key":"10.1016\/j.nbd.2022.105718_bb1145","doi-asserted-by":"crossref","first-page":"1173","DOI":"10.1136\/archdischild-2014-307962","article-title":"Recent advances in the management of Duchenne muscular dystrophy","volume":"100","author":"Strehle","year":"2015","journal-title":"Arch. Dis. Child."},{"key":"10.1016\/j.nbd.2022.105718_bb1150","doi-asserted-by":"crossref","first-page":"435","DOI":"10.1083\/jcb.200105003","article-title":"A stoichiometric complex of neurexins and dystroglycan in brain","volume":"154","author":"Sugita","year":"2001","journal-title":"J. Cell Biol."},{"key":"10.1016\/j.nbd.2022.105718_bb1155","doi-asserted-by":"crossref","first-page":"43","DOI":"10.1007\/s12035-011-8218-9","article-title":"Dystrophin Dp71: the smallest but multifunctional product of the Duchenne muscular dystrophy gene","volume":"45","author":"Tadayoni","year":"2012","journal-title":"Mol. Neurobiol."},{"key":"10.1016\/j.nbd.2022.105718_bb1160","doi-asserted-by":"crossref","first-page":"2940","DOI":"10.3390\/jcm9092940","article-title":"Longitudinal evaluation of working memory in Duchenne muscular dystrophy","volume":"9","author":"Thangarajh","year":"2020","journal-title":"J. Clin. Med."},{"key":"10.1016\/j.nbd.2022.105718_bb1165","doi-asserted-by":"crossref","first-page":"521.524","DOI":"10.1093\/hmg\/2.5.521","article-title":"Apo-dystrophin-3: a 2.2 kb transcript from the DMD locus encoding the dystrophin glycoprotein binding site","volume":"2","author":"Tinsley","year":"1993","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.nbd.2022.105718_bb1170","doi-asserted-by":"crossref","first-page":"287","DOI":"10.1007\/s12035-012-8233-5","article-title":"The shortest isoform of dystrophin (Dp40) interacts with a group of presynaptic proteins to form a presumptive novel complex in the mouse brain","volume":"45","author":"Tozawa","year":"2012","journal-title":"Mol. Neurobiol."},{"key":"10.1016\/j.nbd.2022.105718_bb1175","doi-asserted-by":"crossref","first-page":"1260","DOI":"10.1016\/S0140-6736(95)90923-0","article-title":"Brain abnormalities in Duchenne muscular dystrophy: phosphorus-31 magnetic resonance spectroscopy and neuropsychological study","volume":"345","author":"Tracey","year":"1995","journal-title":"Lancet"},{"key":"10.1016\/j.nbd.2022.105718_bb1180","first-page":"124","article-title":"Personal and social adjustment of children with muscular dystrophy","volume":"34","author":"Truitt","year":"1955","journal-title":"Am. J. Phys. Med."},{"key":"10.1016\/j.nbd.2022.105718_bb1185","doi-asserted-by":"crossref","first-page":"257","DOI":"10.1002\/mus.21559","article-title":"Mitochondrial respiratory chain and creatine kinase activities in mdx mouse brain","volume":"41","author":"Tuon","year":"2010","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.nbd.2022.105718_bb1190","doi-asserted-by":"crossref","first-page":"735","DOI":"10.1038\/335735a0","article-title":"Increased protein degradation results from elevated free calcium levels found in muscle from mdx mice","volume":"335","author":"Turner","year":"1988","journal-title":"Nature"},{"key":"10.1016\/j.nbd.2022.105718_bb1195","doi-asserted-by":"crossref","DOI":"10.1101\/cshperspect.a005736","article-title":"Homeostatic synaptic plasticity: Local and global mechanisms for stabilizing neuronal function","volume":"4","author":"Turrigiano","year":"2012","journal-title":"Cold Spring Harb. Perspect. Biol."},{"key":"10.1016\/j.nbd.2022.105718_bb1200","doi-asserted-by":"crossref","first-page":"11989","DOI":"10.1038\/s41598-020-68381-9","article-title":"Computational cognitive modeling and validation of Dp140 induced alteration of working memory in Duchenne Muscular Dystrophy","volume":"10","author":"Tyagi","year":"2020","journal-title":"Sci. Rep."},{"key":"10.1016\/j.nbd.2022.105718_bb1205","doi-asserted-by":"crossref","first-page":"129","DOI":"10.1007\/BF00296181","article-title":"Dystrophin and dystrophin-related protein in the central nervous system of normal controls and Duchenne muscular dystrophy","volume":"87","author":"Uchino","year":"1994","journal-title":"Acta Neuropathol."},{"key":"10.1016\/j.nbd.2022.105718_bb1210","doi-asserted-by":"crossref","first-page":"426","DOI":"10.1136\/jnnp.57.4.426","article-title":"Localisation and characterisation of dystrophin in the central nervous system of controls and patients with Duchenne muscular dystrophy","volume":"57","author":"Uchino","year":"1994","journal-title":"J. Neurol. Neurosurg. Psychiatry"},{"key":"10.1016\/j.nbd.2022.105718_bb1215","doi-asserted-by":"crossref","first-page":"243","DOI":"10.1007\/s004180050164","article-title":"Dystrophin in rod spherules; submembranous dense regions facing bipolar cell processes","volume":"108","author":"Ueda","year":"1997","journal-title":"Histochem. Cell Biol."},{"key":"10.1016\/j.nbd.2022.105718_bb1220","first-page":"1627","article-title":"Immunocytochemical study of dystrophin localization in cone cells of mouse retinas","volume":"38","author":"Ueda","year":"1997","journal-title":"Invest. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.nbd.2022.105718_bb1225","first-page":"753","article-title":"Current knowledge of dystrophin and dystrophin-associated proteins in the retina","volume":"15","author":"Ueda","year":"2000","journal-title":"Histol. Histopathol."},{"key":"10.1016\/j.nbd.2022.105718_bb1230","doi-asserted-by":"crossref","DOI":"10.7554\/eLife.50712","article-title":"Essential role for InSyn1 in dystroglycan complex integrity and cognitive behaviors in mice","volume":"8","author":"Uezu","year":"2019","journal-title":"eLife"},{"key":"10.1016\/j.nbd.2022.105718_bb1235","doi-asserted-by":"crossref","first-page":"713","DOI":"10.1002\/hipo.10068","article-title":"Facilitated CA1 hippocampal synaptic plasticity in dystrophin-deficient mice: Role for GABAA Receptors?","volume":"12","author":"Vaillend","year":"2002","journal-title":"Hippocampus"},{"key":"10.1016\/j.nbd.2022.105718_bb1240","first-page":"1041","article-title":"Relationships linking emotional, motor, cognitive and GABAergic dysfunctions in dystrophin-deficient mdx mice","volume":"26","author":"Vaillend","year":"2017","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.nbd.2022.105718_bb1245","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1016\/S0306-4522(98)00023-2","article-title":"Spatial discrimination learning and CA1 hippocampal synaptic plasticity in mdx and mdx3cv mice lacking dystrophin-brain isoforms","volume":"86","author":"Vaillend","year":"1998","journal-title":"Neuroscience"},{"key":"10.1016\/j.nbd.2022.105718_bb1250","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1016\/S0306-4522(98)00023-2","article-title":"Spatial discrimination learning and CA1 hippocampal synaptic plasticity in mdx and mdx3cv mice lacking dystrophin gene products","volume":"86","author":"Vaillend","year":"1999","journal-title":"Neuroscience"},{"key":"10.1016\/j.nbd.2022.105718_bb1255","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1002\/(SICI)1098-2396(199907)33:1<59::AID-SYN6>3.0.CO;2-K","article-title":"Facilitated NMDA receptor mediated synaptic plasticity in the hippocampal CA1 area of dystrophin-deficient mice","volume":"33","author":"Vaillend","year":"1999","journal-title":"Synapse"},{"key":"10.1016\/j.nbd.2022.105718_bb1260","doi-asserted-by":"crossref","first-page":"613","DOI":"10.2174\/1566524023361952","article-title":"Gene control of synaptic plasticity and memory formation: implications for diseases and therapeutic strategies","volume":"2","author":"Vaillend","year":"2002","journal-title":"Curr. Mol. Med."},{"key":"10.1016\/j.nbd.2022.105718_bb1265","doi-asserted-by":"crossref","first-page":"10","DOI":"10.1016\/j.nbd.2004.05.004","article-title":"Impaired long-term spatial and recognition memory and enhanced CA1 hippocampal LTP in the dystrophin deficient Dmdmdx mouse","volume":"17","author":"Vaillend","year":"2004","journal-title":"Neurobiol. Dis."},{"key":"10.1016\/j.nbd.2022.105718_bb1270","doi-asserted-by":"crossref","first-page":"1683","DOI":"10.1038\/mt.2010.134","article-title":"Rescue of a dystrophin-like protein by exon skipping in vivo restores GABAA-receptor clustering in the hippocampus of the mdx mouse","volume":"18","author":"Vaillend","year":"2010","journal-title":"Mol. Ther."},{"key":"10.1016\/j.nbd.2022.105718_bb1275","doi-asserted-by":"crossref","first-page":"1623","DOI":"10.1111\/ejn.13249","article-title":"Characterization of neuromuscular synapse function abnormalities in multiple Duchenne muscular dystrophy mouse models","volume":"43","author":"van der Pijl","year":"2016","journal-title":"Eur. J. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb1280","doi-asserted-by":"crossref","first-page":"427","DOI":"10.1016\/j.nmd.2018.02.013","article-title":"Low dystrophin levels and insufficient to normalize the neuromuscular synaptic abnormalities of mdx mice","volume":"28","author":"van der Pijl","year":"2018","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb1285","doi-asserted-by":"crossref","first-page":"333","DOI":"10.1523\/JNEUROSCI.4069-05.2006","article-title":"Dystrophin is required for appropriate retrograde control of neurotransmitter release at the Drosophila neuromuscular junction","volume":"26","author":"van der Plas","year":"2006","journal-title":"J. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb1290","doi-asserted-by":"crossref","first-page":"449","DOI":"10.1078\/0171-9335-00410","article-title":"Neuroligin 2 is exclusively localized to inhibitory synapses","volume":"83","author":"Varoqueaux","year":"2004","journal-title":"Eur. J. Cell Biol."},{"key":"10.1016\/j.nbd.2022.105718_bb1295","first-page":"215","article-title":"Intellectual function and educational achievements in Duchenne muscular dystrophy","volume":"13","author":"Vignos","year":"1977","journal-title":"Isr. J. Med. Sci."},{"key":"10.1016\/j.nbd.2022.105718_bb1300","doi-asserted-by":"crossref","first-page":"3781","DOI":"10.1523\/JNEUROSCI.0478-08.2008","article-title":"Synaptic defects in a Drosophila model of congenital muscular dystrophy","volume":"28","author":"Wairkar","year":"2008","journal-title":"J. Neurosci."},{"key":"10.1016\/j.nbd.2022.105718_bb1305","doi-asserted-by":"crossref","first-page":"344","DOI":"10.1080\/07853890802668522","article-title":"The neurobiology of the dystrophin-associated glycoprotein complex","volume":"41","author":"Waite","year":"2009","journal-title":"Ann. Med."},{"key":"10.1016\/j.nbd.2022.105718_bb1310","doi-asserted-by":"crossref","first-page":"74","DOI":"10.2741\/1209","article-title":"For want of a nail. ramifications of a single gene deletion, dystrophin, in the brain of the mouse","volume":"9","author":"Wallis","year":"2004","journal-title":"Front. Biosci."},{"key":"10.1016\/j.nbd.2022.105718_bb1315","doi-asserted-by":"crossref","first-page":"169","DOI":"10.1093\/brain\/77.2.169","article-title":"On the classification, natural history and treatment of myopathies","volume":"77","author":"Walton","year":"1954","journal-title":"Brain"},{"key":"10.1016\/j.nbd.2022.105718_bb1320","doi-asserted-by":"crossref","first-page":"7901","DOI":"10.1167\/iovs.11-7519","article-title":"Reevaluation of dystrophin localization in the mouse retina","volume":"52","author":"Wersinger","year":"2011","journal-title":"Invest. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.nbd.2022.105718_bb1325","doi-asserted-by":"crossref","first-page":"H1463","DOI":"10.1152\/ajpheart.00176.2015","article-title":"Protein assemblies of sodium and inward rectifier potassium channels control cardiac excitability and arrhythmogenesis","volume":"308","author":"Willis","year":"2015","journal-title":"Am. J. Physiol. Heart Circ. Physiol."},{"key":"10.1016\/j.nbd.2022.105718_bb1330","doi-asserted-by":"crossref","first-page":"241","DOI":"10.1016\/j.nmd.2008.11.015","article-title":"Mammalian animal models for Duchenne muscular dystrophy","volume":"19","author":"Willmann","year":"2009","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.nbd.2022.105718_bb1335","doi-asserted-by":"crossref","first-page":"675","DOI":"10.1083\/jcb.140.3.675","article-title":"Beta-spectrin is colocalized with both voltage-gated sodium channels and ankyrinG at the adult rat neuromuscular junction","volume":"140","author":"Wood","year":"1998","journal-title":"J. Cell Biol."},{"key":"10.1016\/j.nbd.2022.105718_bb1340","doi-asserted-by":"crossref","first-page":"968","DOI":"10.1542\/peds.29.6.968","article-title":"Intellectual function in childhood progressive muscular dystrophy","volume":"29","author":"Worden","year":"1962","journal-title":"Pediatrics"},{"key":"10.1016\/j.nbd.2022.105718_bb1345","doi-asserted-by":"crossref","first-page":"11711","DOI":"10.1074\/jbc.270.20.11711","article-title":"SH3 domain-mediated interaction of dystroglycan and Grb2","volume":"270","author":"Yang","year":"1995","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.nbd.2022.105718_bb1350","doi-asserted-by":"crossref","first-page":"768","DOI":"10.1097\/00005072-199808000-00006","article-title":"Disassembly of the cholinergic postsynaptic apparatus induced by axotomy in mouse sympathetic neurons: loss of dystrophin and \u03b2-dystroglycan immunoreactivity precedes that of the acetylcholine receptor","volume":"57","author":"Zaccaria","year":"1998","journal-title":"J. Neuropathol. Exp. Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb1355","doi-asserted-by":"crossref","first-page":"103","DOI":"10.1093\/jnen\/59.2.103","article-title":"Selective reduction in the nicotinic acetylcholine receptor and dystroglycan at the postsynaptic apparatus of mdx mouse superior cervical ganglion","volume":"59","author":"Zaccaria","year":"2000","journal-title":"J. Neuropathol. Exp. Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb1360","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0016911","article-title":"Presynaptic nicotinic alpha7 and non-alpha7 receptors stimulate endogenous GABA release from rat hippocampal synaptosomes through two mechanisms of action","volume":"6","author":"Zappettini","year":"2011","journal-title":"PLoS One"},{"key":"10.1016\/j.nbd.2022.105718_bb1365","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1136\/jmg.30.2.131","article-title":"Cosegregation of schizophrenia with Becker muscular dystrophy: susceptibility locus for schizophrenia at Xp21 or an effect of the dystrophin gene in the brain?","volume":"30","author":"Zatz","year":"1993","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.nbd.2022.105718_bb1370","doi-asserted-by":"crossref","first-page":"576","DOI":"10.1111\/j.1469-8749.1967.tb02327.x","article-title":"Psychometric studies in muscular dystrophy type Illa (Duchenne)","volume":"9","author":"Zellweger","year":"1967","journal-title":"Dev. Med. Child Neurol."},{"key":"10.1016\/j.nbd.2022.105718_bb1375","first-page":"25","article-title":"Central nervous system manifestation s in childhood muscular dystrophy (CMD), 1. Psychometric and electroencephalographic findings","volume":"205","author":"Zellweger","year":"1965","journal-title":"Ann. Pediatr."},{"key":"10.1016\/j.nbd.2022.105718_bb1380","doi-asserted-by":"crossref","first-page":"66","DOI":"10.1038\/ng709","article-title":"Mutations in the gene encoding epsilon sarcoglycan cause myoclonus-dystonia syndrome","volume":"29","author":"Zimprich","year":"2001","journal-title":"Nat. Genet."}],"container-title":["Neurobiology of Disease"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0969996122001103?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0969996122001103?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T05:34:55Z","timestamp":1760852095000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0969996122001103"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,6]]},"references-count":272,"alternative-id":["S0969996122001103"],"URL":"https:\/\/doi.org\/10.1016\/j.nbd.2022.105718","relation":{},"ISSN":["0969-9961"],"issn-type":[{"value":"0969-9961","type":"print"}],"subject":[],"published":{"date-parts":[[2022,6]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Synaptic alterations as a neurodevelopmental trait of Duchenne muscular dystrophy","name":"articletitle","label":"Article Title"},{"value":"Neurobiology of Disease","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.nbd.2022.105718","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2022 The Authors. Published by Elsevier Inc.","name":"copyright","label":"Copyright"}],"article-number":"105718"}}