{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,1]],"date-time":"2026-04-01T22:50:17Z","timestamp":1775083817506,"version":"3.50.1"},"reference-count":23,"publisher":"Elsevier BV","issue":"10","license":[{"start":{"date-parts":[[2009,10,1]],"date-time":"2009-10-01T00:00:00Z","timestamp":1254355200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2009,10,1]],"date-time":"2009-10-01T00:00:00Z","timestamp":1254355200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Clinical Neurophysiology"],"published-print":{"date-parts":[[2009,10]]},"DOI":"10.1016\/j.clinph.2009.07.042","type":"journal-article","created":{"date-parts":[[2009,8,24]],"date-time":"2009-08-24T04:08:35Z","timestamp":1251086915000},"page":"1782-1786","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":11,"title":["Electroencephalography in autosomal dominant adult neuronal ceroid lipofuscinosis"],"prefix":"10.1016","volume":"120","author":[{"given":"P.C.G.","family":"Nijssen","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G.J.F.","family":"Brekelmans","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.A.C.","family":"Roos","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"6","key":"10.1016\/j.clinph.2009.07.042_bib1","first-page":"222","article-title":"Our experience with Kufs disease: familial form and sporadic case","volume":"6","author":"Arpa","year":"1991","journal-title":"Neurologia"},{"issue":"Pt. 1","key":"10.1016\/j.clinph.2009.07.042_bib2","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1093\/brain\/111.1.27","article-title":"Kufs\u2019 disease: a critical reappraisal","volume":"111","author":"Berkovic","year":"1988","journal-title":"Brain"},{"issue":"3 Suppl.","key":"10.1016\/j.clinph.2009.07.042_bib3","doi-asserted-by":"crossref","first-page":"S83","DOI":"10.1007\/s100720070045","article-title":"Electroencephalographic features in a series of patients with neuronal ceroid lipofuscinoses","volume":"21","author":"Binelli","year":"2000","journal-title":"Neurol Sci"},{"issue":"4","key":"10.1016\/j.clinph.2009.07.042_bib4","doi-asserted-by":"crossref","first-page":"745","DOI":"10.1093\/brain\/94.4.745","article-title":"A dominant form of neuronal ceroid-lipofuscinosis","volume":"94","author":"Boehme","year":"1971","journal-title":"Brain"},{"key":"10.1016\/j.clinph.2009.07.042_bib5","first-page":"305","article-title":"On the neurochemistry of an adult form of ceroid lipofuscinosis (Kuf\u2019s disease)","volume":"39","author":"Boehme","year":"1980","journal-title":"Prog Clin Biol Res"},{"issue":"3","key":"10.1016\/j.clinph.2009.07.042_bib7","doi-asserted-by":"crossref","first-page":"231","DOI":"10.1136\/jnnp.39.3.231","article-title":"A dominant form of adult neuronal ceroidlipofuscinosis (Kufs\u2019 disease) with an associated occipital astrocytoma: early diagnosis by cortical biopsy","volume":"39","author":"Brodner","year":"1976","journal-title":"J Neurol Neurosurg Psychiatry"},{"issue":"3","key":"10.1016\/j.clinph.2009.07.042_bib8","doi-asserted-by":"crossref","first-page":"183","DOI":"10.1007\/BF00313117","article-title":"A Golgi and ultrastructural study of a dominant form of Kufs\u2019 disease","volume":"222","author":"Ferrer","year":"1980","journal-title":"J Neurol"},{"key":"10.1016\/j.clinph.2009.07.042_bib10","doi-asserted-by":"crossref","first-page":"128","DOI":"10.1097\/01.WNP.0000158701.89576.4C","article-title":"The ACNS subcommittee on research terminology for continuous EEG monitoring: proposed standardized terminology for rhythmic and periodic EEG patterns encountered in critically ill patients","volume":"22","author":"Hirsch","year":"2005","journal-title":"J Clin Neurophysiol"},{"issue":"1\u20132","key":"10.1016\/j.clinph.2009.07.042_bib11","doi-asserted-by":"crossref","first-page":"51","DOI":"10.1016\/S0022-510X(01)00546-9","article-title":"Autosomal dominant Kufs\u2019 disease: a cause of early onset dementia","volume":"188","author":"Josephson","year":"2001","journal-title":"J Neurol Sci"},{"issue":"2","key":"10.1016\/j.clinph.2009.07.042_bib12","doi-asserted-by":"crossref","first-page":"100","DOI":"10.1055\/s-2008-1046591","article-title":"EEG in diagnosis of other disease pictures than epilepsy","volume":"206","author":"Kurlemann","year":"1994","journal-title":"Klin Padiatr"},{"issue":"5","key":"10.1016\/j.clinph.2009.07.042_bib13","first-page":"507","article-title":"Myoclonic-astatic seizures (Lennox syndrome) in the course of juvenile neuronal ceroid-lipofuscinosis [Batten-Spielmeyer-Vogt M, Trans.]","volume":"190","author":"Lagenstein","year":"1978","journal-title":"Klin Padiatr"},{"issue":"10","key":"10.1016\/j.clinph.2009.07.042_bib14","doi-asserted-by":"crossref","first-page":"975","DOI":"10.1212\/WNL.21.10.975","article-title":"Pseudoperiodic lateralized paroxysmal discharges in electroencephalogram","volume":"21","author":"Markand","year":"1971","journal-title":"Neurology"},{"issue":"9177","key":"10.1016\/j.clinph.2009.07.042_bib15","doi-asserted-by":"crossref","first-page":"443","DOI":"10.1016\/S0140-6736(99)00173-7","article-title":"Batten\u2019s disease: eight genes and still counting?","volume":"354","author":"Mole","year":"1999","journal-title":"Lancet"},{"issue":"1","key":"10.1016\/j.clinph.2009.07.042_bib16","doi-asserted-by":"crossref","first-page":"70","DOI":"10.1111\/j.1750-3639.2004.tb00500.x","article-title":"The genetic spectrum of human neuronal ceroid-lipofuscinoses","volume":"14","author":"Mole","year":"2004","journal-title":"Brain Pathol"},{"issue":"3","key":"10.1016\/j.clinph.2009.07.042_bib17","doi-asserted-by":"crossref","first-page":"482","DOI":"10.1002\/mds.10104","article-title":"Autosomal dominant adult neuronal ceroid lipofuscinosis: Parkinsonism due to both striatal and nigral dysfunction","volume":"17","author":"Nijssen","year":"2002","journal-title":"Mov Disord"},{"issue":"4","key":"10.1016\/j.clinph.2009.07.042_bib18","doi-asserted-by":"crossref","first-page":"574","DOI":"10.1111\/j.1750-3639.2003.tb00486.x","article-title":"Autosomal dominant adult neuronal ceroid lipofuscinosis: a novel form of NCL with granular osmiophilic deposits without palmitoyl protein thioesterase 1 deficiency","volume":"13","author":"Nijssen","year":"2003","journal-title":"Brain Pathol"},{"issue":"1","key":"10.1016\/j.clinph.2009.07.042_bib19","doi-asserted-by":"crossref","first-page":"70","DOI":"10.1055\/s-2007-973673","article-title":"Neurophysiological findings in neuronal ceroid lipofuscinoses","volume":"28","author":"Sainio","year":"1997","journal-title":"Neuropediatrics"},{"issue":"1","key":"10.1016\/j.clinph.2009.07.042_bib20","doi-asserted-by":"crossref","first-page":"61","DOI":"10.1111\/j.1469-8749.1992.tb08564.x","article-title":"MRI of the brain, EEG sleep spindles and SPECT in the early diagnosis of infantile neuronal ceroid lipofuscinosis","volume":"34","author":"Santavuori","year":"1992","journal-title":"Dev Med Child Neurol"},{"issue":"9","key":"10.1016\/j.clinph.2009.07.042_bib21","doi-asserted-by":"crossref","first-page":"1738","DOI":"10.1016\/S1388-2457(03)00111-1","article-title":"Electroencephalographic findings in Kufs disease","volume":"114","author":"Vadlamudi","year":"2003","journal-title":"Clin Neurophysiol"},{"issue":"7","key":"10.1016\/j.clinph.2009.07.042_bib22","doi-asserted-by":"crossref","first-page":"456","DOI":"10.1111\/j.1469-8749.1997.tb07465.x","article-title":"EEG and evoked potentials in infantile neuronal ceroid-lipofuscinosis","volume":"39","author":"Vanhanen","year":"1997","journal-title":"Dev Med Child Neurol"},{"issue":"5","key":"10.1016\/j.clinph.2009.07.042_bib23","doi-asserted-by":"crossref","first-page":"306","DOI":"10.1016\/S0387-7604(01)00231-5","article-title":"Clinical and EEG findings in 18 cases of late infantile neuronal ceroid lipofuscinosis","volume":"23","author":"Veneselli","year":"2001","journal-title":"Brain Dev"},{"issue":"4","key":"10.1016\/j.clinph.2009.07.042_bib24","doi-asserted-by":"crossref","first-page":"398","DOI":"10.1006\/mgme.1999.2807","article-title":"Ultrastructural and electrophysiological correlation of the genotypes of NCL","volume":"66","author":"Williams","year":"1999","journal-title":"Mol Genet Metab"},{"issue":"3","key":"10.1016\/j.clinph.2009.07.042_bib25","doi-asserted-by":"crossref","first-page":"155","DOI":"10.1055\/s-2008-1071534","article-title":"New subform of the late infantile form of neuronal ceroid lipofuscinosis","volume":"24","author":"Wisniewski","year":"1993","journal-title":"Neuropediatrics"}],"container-title":["Clinical Neurophysiology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1388245709004817?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1388245709004817?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,25]],"date-time":"2025-10-25T10:52:30Z","timestamp":1761389550000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1388245709004817"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,10]]},"references-count":23,"journal-issue":{"issue":"10","published-print":{"date-parts":[[2009,10]]}},"alternative-id":["S1388245709004817"],"URL":"https:\/\/doi.org\/10.1016\/j.clinph.2009.07.042","relation":{},"ISSN":["1388-2457"],"issn-type":[{"value":"1388-2457","type":"print"}],"subject":[],"published":{"date-parts":[[2009,10]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Electroencephalography in autosomal dominant adult neuronal ceroid lipofuscinosis","name":"articletitle","label":"Article Title"},{"value":"Clinical Neurophysiology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.clinph.2009.07.042","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2009 International Federation of Clinical Neurophysiology. Published by Elsevier Ireland Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}