{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,31]],"date-time":"2025-12-31T20:05:07Z","timestamp":1767211507891,"version":"3.40.5"},"reference-count":23,"publisher":"Elsevier BV","issue":"1-2","license":[{"start":{"date-parts":[[2019,1,1]],"date-time":"2019-01-01T00:00:00Z","timestamp":1546300800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Revue Neurologique"],"published-print":{"date-parts":[[2019,1]]},"DOI":"10.1016\/j.neurol.2018.04.009","type":"journal-article","created":{"date-parts":[[2018,11,5]],"date-time":"2018-11-05T09:06:31Z","timestamp":1541408791000},"page":"81-86","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":9,"title":["O'Sullivan\u2013McLeod syndrome: Unmasking a rare atypical motor neuron disease"],"prefix":"10.1016","volume":"175","author":[{"given":"W.B.V.R.","family":"Pinto","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P.P.","family":"Nunes","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I.","family":"Lima e Teixeira","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.C.D.","family":"Assis","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1824-9993","authenticated-orcid":false,"given":"F.G.M.","family":"Naylor","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.A.T.","family":"Chieia","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7416-7108","authenticated-orcid":false,"given":"P.V.S.","family":"Souza","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6986-4937","authenticated-orcid":false,"family":"A.S.B. Oliveira","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.neurol.2018.04.009_bib0120","article-title":"Differential diagnosis and atypical subsets of amyotrophic lateral sclerosis","volume":"162","author":"Pradat","year":"2006","journal-title":"Rev Neurol"},{"key":"10.1016\/j.neurol.2018.04.009_bib0125","doi-asserted-by":"crossref","first-page":"474","DOI":"10.1136\/jnnp-2016-313526","article-title":"Differentiating lower motor neuron syndromes","volume":"88","author":"Garg","year":"2017","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"10.1016\/j.neurol.2018.04.009_bib0130","doi-asserted-by":"crossref","first-page":"654","DOI":"10.1007\/PL00007808","article-title":"Slowly progressive spinal muscular atrophy of the hands (O'Sullivan-McLeod syndrome): clinical and magnetic resonance imaging presentation","volume":"247","author":"Petiot","year":"2000","journal-title":"J Neurol"},{"key":"10.1016\/j.neurol.2018.04.009_bib0135","doi-asserted-by":"crossref","first-page":"653","DOI":"10.1136\/jnnp.41.7.653","article-title":"Distal chronic spinal muscular atrophy involving the hands","volume":"41","author":"O'Sullivan","year":"1978","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"10.1016\/j.neurol.2018.04.009_bib0140","first-page":"368","volume":"140","author":"Serratrice","year":"1984","journal-title":"Chronic distal spinal amyotrophy localized to the both upper limbs (O'Sullivan and McLeod type). Rev Neurol (Paris)"},{"key":"10.1016\/j.neurol.2018.04.009_bib0145","first-page":"43","article-title":"Bilateral distal muscular atrophy of upper limbs (O'Sullivan-McLeod syndrome). Case report","volume":"46","author":"Orsini","year":"2010","journal-title":"Rev Bras Neurol"},{"key":"10.1016\/j.neurol.2018.04.009_bib0150","first-page":"320","volume":"173","author":"Verschueren","year":"2017","journal-title":"Motor neuropathies and lower motor neuron syndromes. Rev Neurol (Paris)"},{"key":"10.1016\/j.neurol.2018.04.009_bib0155","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1136\/practneurol-2013-000557","article-title":"Mimics and chameleons in motor neurone disease","volume":"13","author":"Turner","year":"2013","journal-title":"Pract Neurol"},{"key":"10.1016\/j.neurol.2018.04.009_bib0160","doi-asserted-by":"crossref","first-page":"373","DOI":"10.1212\/WNL.13.5.373","article-title":"Juvenile muscular atrophy of unilateral upper extremity: a new clinical entity","volume":"13","author":"Hirayama","year":"1959","journal-title":"Neurology"},{"key":"10.1016\/j.neurol.2018.04.009_bib0165","doi-asserted-by":"crossref","first-page":"338","DOI":"10.1016\/j.neurol.2017.03.016","volume":"173","author":"Cintas","year":"2017","journal-title":"Benign focal amyotrophy. Rev Neurol (Paris)"},{"key":"10.1016\/j.neurol.2018.04.009_bib0170","doi-asserted-by":"crossref","first-page":"327","DOI":"10.3109\/17453676808989466","article-title":"Unilateral juvenile muscular atrophy of upper limbs","volume":"39","author":"Pilgaard","year":"1968","journal-title":"Acta Orthop Scand"},{"key":"10.1016\/j.neurol.2018.04.009_bib0175","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1002\/mus.20811","article-title":"Late-onset monomelic amyotrophy in a Caucasian woman","volume":"37","author":"Patel","year":"2008","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.neurol.2018.04.009_bib0180","doi-asserted-by":"crossref","first-page":"337","DOI":"10.1016\/0022-510X(80)90177-X","article-title":"Hereditary distal spinal muscular atrophy. A report on 34 cases and a review of the literature","volume":"45","author":"Harding","year":"1980","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.neurol.2018.04.009_bib0185","first-page":"163","article-title":"Chronic spinal amyotrophy involving the upper limbs in young adults (O'Sullivan and McLeod syndrome). MRI study of the cervical spinal cord","volume":"145","author":"Gaio","year":"1989","journal-title":"Rev Neurol (Paris)"},{"key":"10.1016\/j.neurol.2018.04.009_bib0190","first-page":"254","volume":"173","author":"Corcia","year":"2017","journal-title":"Genetics of Amyotrophic Lateral Sclerosis. Rev Neurol (Paris)"},{"key":"10.1016\/j.neurol.2018.04.009_bib0195","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1038\/nn.3584","article-title":"State of play in amyotrophic lateral sclerosis genetics","volume":"17","author":"Renton","year":"2014","journal-title":"Nat Neurosci"},{"key":"10.1016\/j.neurol.2018.04.009_bib0200","doi-asserted-by":"crossref","first-page":"1026","DOI":"10.1590\/0004-282X20150161","article-title":"Clinical and genetic basis of familial amyotrophic lateral sclerosis","volume":"73","author":"Souza","year":"2015","journal-title":"Arq Neuropsiquiatr"},{"key":"10.1016\/j.neurol.2018.04.009_bib0205","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1055\/s-2001-15263","article-title":"Atypical motor neuron disease and related motor syndromes","volume":"21","author":"Verma","year":"2001","journal-title":"Semin Neurol"},{"key":"10.1016\/j.neurol.2018.04.009_bib0210","doi-asserted-by":"crossref","first-page":"14","DOI":"10.1016\/j.jns.2014.10.013","article-title":"Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an update","volume":"347","author":"Tazir","year":"2014","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.neurol.2018.04.009_bib0215","doi-asserted-by":"crossref","first-page":"6","DOI":"10.1136\/jnnp-2011-300952","article-title":"The distal hereditary motor neuropathies","volume":"83","author":"Rossor","year":"2012","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"10.1016\/j.neurol.2018.04.009_bib0220","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.neurol.2018.04.009_bib0225","doi-asserted-by":"crossref","first-page":"712","DOI":"10.12968\/hmed.2014.75.12.712","article-title":"O'Sullivan\u2013McLeod syndrome: clinical features, neuroradiology and nosology","volume":"75","author":"Ghadiri-Sani","year":"2014","journal-title":"Br J Hosp Med (Lond)"},{"key":"10.1016\/j.neurol.2018.04.009_bib0230","doi-asserted-by":"crossref","first-page":"515","DOI":"10.2169\/internalmedicine.46.6221","article-title":"Slowly progressive distal muscular atrophy of the bilateral upper limbs (O'Sullivan-McLeod syndrome) partially alleviated by intravenous immunoglobulin therapy","volume":"46","author":"Kawano","year":"2007","journal-title":"Intern Med"}],"container-title":["Revue Neurologique"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0035378718300092?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0035378718300092?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,3,2]],"date-time":"2019-03-02T08:08:36Z","timestamp":1551514116000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0035378718300092"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,1]]},"references-count":23,"journal-issue":{"issue":"1-2","published-print":{"date-parts":[[2019,1]]}},"alternative-id":["S0035378718300092"],"URL":"https:\/\/doi.org\/10.1016\/j.neurol.2018.04.009","relation":{},"ISSN":["0035-3787"],"issn-type":[{"type":"print","value":"0035-3787"}],"subject":[],"published":{"date-parts":[[2019,1]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"O'Sullivan\u2013McLeod syndrome: Unmasking a rare atypical motor neuron disease","name":"articletitle","label":"Article Title"},{"value":"Revue Neurologique","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.neurol.2018.04.009","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}