{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,1]],"date-time":"2022-04-01T08:24:30Z","timestamp":1648801470093},"reference-count":21,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2008,12,1]],"date-time":"2008-12-01T00:00:00Z","timestamp":1228089600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Seminars in Pediatric Neurology"],"published-print":{"date-parts":[[2008,12]]},"DOI":"10.1016\/j.spen.2008.10.005","type":"journal-article","created":{"date-parts":[[2008,12,14]],"date-time":"2008-12-14T09:45:40Z","timestamp":1229247940000},"page":"186-189","source":"Crossref","is-referenced-by-count":0,"title":["Proximal Muscle Weakness in a 15-Year-Old Boy"],"prefix":"10.1016","volume":"15","author":[{"given":"Marcia V.","family":"Felker","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bhuwan P.","family":"Garg","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.spen.2008.10.005_bib1","series-title":"Pediatric Neurology","first-page":"2023","article-title":"Metabolic myopathies","author":"Tein","year":"2006"},{"key":"10.1016\/j.spen.2008.10.005_bib2","series-title":"Pediatric Neurology","first-page":"2015","article-title":"Congenital myopathies","author":"Strober","year":"2006"},{"key":"10.1016\/j.spen.2008.10.005_bib3","first-page":"33","article-title":"Muscular dystrophies","volume":"12","author":"Darras","year":"2006","journal-title":"Continuum"},{"key":"10.1016\/j.spen.2008.10.005_bib4","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1097\/01.cnd.0000249557.59140.3a","article-title":"A boy with proximal weakness and cardiomyopathy","volume":"8","author":"Mitchell","year":"2006","journal-title":"J Clin Neuromuscul Dis"},{"key":"10.1016\/j.spen.2008.10.005_bib5","doi-asserted-by":"crossref","first-page":"767","DOI":"10.1016\/S0272-2712(18)30604-8","article-title":"Serum enzymes in disease of skeletal muscle","volume":"9","author":"Rosalki","year":"1989","journal-title":"Clin Lab Med"},{"key":"10.1016\/j.spen.2008.10.005_bib6","article-title":"Disability and survival in Duchenne muscular dystrophy","author":"Kohler","year":"2008","journal-title":"J Neurol Neurosurg Psychiatr"},{"key":"10.1016\/j.spen.2008.10.005_bib7","article-title":"Limb-girdle muscular dystrophy overview","author":"Gordon","year":"2007","journal-title":"Gene Review"},{"key":"10.1016\/j.spen.2008.10.005_bib8","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1097\/00131402-200309000-00003","article-title":"The limb girdle muscular dystrophies","volume":"5","author":"Wicklund","year":"2003","journal-title":"J Clinical Neuromuscul Dis"},{"key":"10.1016\/j.spen.2008.10.005_bib9","doi-asserted-by":"crossref","first-page":"500","DOI":"10.1001\/archneurpsyc.1956.02330230050005","article-title":"Heredofamilial juvenile muscular atrophy simulating muscular dystrophy","volume":"75","author":"Kugelberg","year":"1956","journal-title":"AMA Arch Neurol Psychiatr"},{"key":"10.1016\/j.spen.2008.10.005_bib10","doi-asserted-by":"crossref","first-page":"409","DOI":"10.1136\/jmg.15.6.409","article-title":"Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy","volume":"15","author":"Pearn","year":"1978","journal-title":"J Med Genet"},{"key":"10.1016\/j.spen.2008.10.005_bib11","doi-asserted-by":"crossref","first-page":"952","DOI":"10.1177\/0883073807305668","article-title":"Spinal muscular atrophy diagnostics","volume":"22","author":"Prior","year":"2007","journal-title":"J Child Neurol"},{"key":"10.1016\/j.spen.2008.10.005_bib12","doi-asserted-by":"crossref","first-page":"1301","DOI":"10.1177\/0883073807307105","article-title":"A newborn with spinal muscular atrophy type 0 presenting with a clincopathological picture suggestive of myotubular myopathy","volume":"22","author":"Nadeau","year":"2007","journal-title":"J Child Neurol"},{"key":"10.1016\/j.spen.2008.10.005_bib13","doi-asserted-by":"crossref","first-page":"518","DOI":"10.1001\/archneur.1995.00540290108025","article-title":"Natural history in proximal spinal muscular atrophy\u2014clinical analysis of 445 patients and suggestions for a modification of existing classifications","volume":"52","author":"Zerres","year":"1995","journal-title":"Arch Neurol"},{"key":"10.1016\/j.spen.2008.10.005_bib14","doi-asserted-by":"crossref","first-page":"548","DOI":"10.1542\/peds.2004-0668","article-title":"Spinal muscular atrophy: Survival pattern and functional status","volume":"114","author":"Chung","year":"2004","journal-title":"Pediatrics"},{"key":"10.1016\/j.spen.2008.10.005_bib15","doi-asserted-by":"crossref","first-page":"946","DOI":"10.1177\/0883073807305673","article-title":"Spinal muscular atrophy: Clinical classification and disease heterogeneity","volume":"22","author":"Russman","year":"2007","journal-title":"J Child Neurol"},{"key":"10.1016\/j.spen.2008.10.005_bib16","doi-asserted-by":"crossref","first-page":"51","DOI":"10.1016\/j.yexcr.2004.03.022","article-title":"The SMN complex","volume":"296","author":"Gubitz","year":"2004","journal-title":"Exp Cell Res"},{"key":"10.1016\/j.spen.2008.10.005_bib17","doi-asserted-by":"crossref","first-page":"228","DOI":"10.1002\/(SICI)1098-1004(200003)15:3<228::AID-HUMU3>3.0.CO;2-9","article-title":"An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA)","volume":"15","author":"Wirth","year":"2000","journal-title":"Hum Mutat"},{"key":"10.1016\/j.spen.2008.10.005_bib18","doi-asserted-by":"crossref","first-page":"957","DOI":"10.1177\/0883073807305665","article-title":"Perspectives on clinical trials in spinal muscular atrophy","volume":"22","author":"Swoboda","year":"2007","journal-title":"J Child Neurol"},{"key":"10.1016\/j.spen.2008.10.005_bib19","doi-asserted-by":"crossref","first-page":"358","DOI":"10.1086\/338627","article-title":"Quantitative analyses of SMN1 and SMN2 based on real-time lightcycler PCR: Fast and highly reliable carrier testing and prediction of severity of spinal muscular atrophy","volume":"70","author":"Feldkotter","year":"2002","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.spen.2008.10.005_bib20","first-page":"1837","article-title":"Motor neuron diseases in children","author":"Gomez","year":"1994"},{"key":"10.1016\/j.spen.2008.10.005_bib21","doi-asserted-by":"crossref","first-page":"154","DOI":"10.1159\/000007926","article-title":"Analysis of creatine kinase activity in 504 patients with proximal spinal muscular atrophy types I-III from the point of view of progression and severity","volume":"39","author":"Rudnik-Sch\u00f6neborn","year":"1998","journal-title":"Eur Neurol"}],"container-title":["Seminars in Pediatric Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1071909108000806?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1071909108000806?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2020,3,13]],"date-time":"2020-03-13T21:31:40Z","timestamp":1584135100000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1071909108000806"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,12]]},"references-count":21,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2008,12]]}},"alternative-id":["S1071909108000806"],"URL":"https:\/\/doi.org\/10.1016\/j.spen.2008.10.005","relation":{},"ISSN":["1071-9091"],"issn-type":[{"value":"1071-9091","type":"print"}],"subject":[],"published":{"date-parts":[[2008,12]]}}}