{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,1]],"date-time":"2022-04-01T09:19:41Z","timestamp":1648804781042},"reference-count":13,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2012,4,1]],"date-time":"2012-04-01T00:00:00Z","timestamp":1333238400000},"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":["Revue Neurologique"],"published-print":{"date-parts":[[2012,4]]},"DOI":"10.1016\/j.neurol.2011.09.010","type":"journal-article","created":{"date-parts":[[2012,3,5]],"date-time":"2012-03-05T23:13:42Z","timestamp":1330989222000},"page":"367-370","source":"Crossref","is-referenced-by-count":0,"title":["Association non fortuite d\u2019une neutrop\u00e9nie chronique et d\u2019une maladie de Charcot-Marie-Tooth en rapport avec une mutation de la dynamine 2"],"prefix":"10.1016","volume":"168","author":[{"given":"A.","family":"Saint-L\u00e9zer","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G.","family":"Sol\u00e9","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Ribeiro","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P.","family":"Latour","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P.","family":"Merci\u00e9","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Longy-Boursier","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"2","key":"10.1016\/j.neurol.2011.09.010_bib0005","doi-asserted-by":"crossref","first-page":"200","DOI":"10.1016\/j.lpm.2008.07.013","article-title":"Charcot-Marie-Tooth disease","volume":"38","author":"Birouk","year":"2009","journal-title":"Presse Med"},{"issue":"11","key":"10.1016\/j.neurol.2011.09.010_bib0010","doi-asserted-by":"crossref","first-page":"1207","DOI":"10.1038\/ng1657","article-title":"Mutations in dynamin 2\u00a0cause dominant centronuclear myopathy","volume":"37","author":"Bitoun","year":"2005","journal-title":"Nat Genet"},{"issue":"4","key":"10.1016\/j.neurol.2011.09.010_bib0015","doi-asserted-by":"crossref","first-page":"334","DOI":"10.1016\/j.nmd.2008.01.005","article-title":"A novel mutation in the dynamin 2\u00a0gene in a Charcot-Marie-Tooth type 2\u00a0patient: clinical and pathological findings","volume":"18","author":"Bitoun","year":"2008","journal-title":"Neuromuscul Disord"},{"key":"10.1016\/j.neurol.2011.09.010_bib0020","first-page":"389","article-title":"Castaigne. Peroneal muscular atrophy. Part 1. Clinical and electrophysiological study","volume":"61","author":"Bouch\u00e9","year":"1983","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.neurol.2011.09.010_bib0025","doi-asserted-by":"crossref","first-page":"123","DOI":"10.1016\/0022-510X(77)90043-0","article-title":"The peroneal muscular atrophy syndrome. Clinical genetic, electrophysiological and nerve biopsy studies. Part 3. Clinical, electrophysiological and pathological correlations","volume":"32","author":"Bradley","year":"1977","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.neurol.2011.09.010_bib0030","doi-asserted-by":"crossref","first-page":"1741","DOI":"10.1093\/brain\/awp115","article-title":"Phenotypic spectrum of dynamin 2\u00a0mutations in Charcot-Marie-Tooth neuropathy","volume":"132","author":"Claeys","year":"2009","journal-title":"Brain"},{"issue":"4","key":"10.1016\/j.neurol.2011.09.010_bib0035","doi-asserted-by":"crossref","first-page":"339","DOI":"10.1007\/s00109-009-0587-4","article-title":"Dynamin 2\u00a0and human diseases","volume":"88","author":"Durieux","year":"2010","journal-title":"J Mol Med"},{"key":"10.1016\/j.neurol.2011.09.010_bib0040","doi-asserted-by":"crossref","first-page":"291","DOI":"10.1212\/01.wnl.0000265820.51075.61","article-title":"Two novel mutations in dynamin-2\u00a0cause axonal Charcot-Marie-Tooth disease","volume":"69","author":"Fabrizi","year":"2007","journal-title":"Neurology"},{"key":"10.1016\/j.neurol.2011.09.010_bib0045","doi-asserted-by":"crossref","first-page":"3427","DOI":"10.1242\/jcs.051714","article-title":"Dynamins at a glance","volume":"122","author":"Heymann","year":"2009","journal-title":"J Cell Sci"},{"issue":"12","key":"10.1016\/j.neurol.2011.09.010_bib0050","doi-asserted-by":"crossref","first-page":"801","DOI":"10.1016\/j.nmd.2010.07.273","article-title":"Sporadic centronuclear myopathy with muscle pseudohypertrophy, neutropenia, and necklace fibers due to a DNM2\u00a0mutation","volume":"20","author":"Liewluck","year":"2010","journal-title":"Neuromuscul Disord"},{"issue":"2","key":"10.1016\/j.neurol.2011.09.010_bib0055","doi-asserted-by":"crossref","first-page":"148","DOI":"10.1016\/j.nmd.2010.11.009","article-title":"Sporadic centronuclear myopathy with muscle pseudohypertrophy, neutropenia, and necklace fibres due to a DNM2\u00a0mutation","volume":"21","author":"Romero","year":"2011","journal-title":"Neuromuscul Disord"},{"key":"10.1016\/j.neurol.2011.09.010_bib0060","doi-asserted-by":"crossref","first-page":"98","DOI":"10.1111\/j.1399-0004.1974.tb00638.x","article-title":"Genetic and clinical aspects of Charcot-Marie-Tooth'sdisease","volume":"6","author":"Skre","year":"1974","journal-title":"Clin Genet"},{"issue":"3","key":"10.1016\/j.neurol.2011.09.010_bib0065","doi-asserted-by":"crossref","first-page":"289","DOI":"10.1038\/ng1514","article-title":"Mutations in the pleckstrin homology domain of dynamin 2\u00a0cause dominant intermediate Charcot-Marie-Tooth disease","volume":"37","author":"Z\u00fcchner","year":"2005","journal-title":"Nat Genet"}],"container-title":["Revue Neurologique"],"original-title":[],"language":"fr","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0035378712003967?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0035378712003967?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,11,25]],"date-time":"2018-11-25T09:24:41Z","timestamp":1543137881000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0035378712003967"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,4]]},"references-count":13,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2012,4]]}},"alternative-id":["S0035378712003967"],"URL":"https:\/\/doi.org\/10.1016\/j.neurol.2011.09.010","relation":{},"ISSN":["0035-3787"],"issn-type":[{"value":"0035-3787","type":"print"}],"subject":[],"published":{"date-parts":[[2012,4]]}}}