{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T19:30:37Z","timestamp":1786995037565,"version":"build-2736575974"},"reference-count":12,"publisher":"Elsevier BV","issue":"10","license":[{"start":{"date-parts":[[2015,10,1]],"date-time":"2015-10-01T00:00:00Z","timestamp":1443657600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2015,10,1]],"date-time":"2015-10-01T00:00:00Z","timestamp":1443657600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"funder":[{"DOI":"10.13039\/501100009882","name":"Regione Lombardia","doi-asserted-by":"crossref","id":[{"id":"10.13039\/501100009882","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","nmd-journal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Neuromuscular Disorders"],"published-print":{"date-parts":[[2015,10]]},"DOI":"10.1016\/j.nmd.2015.07.015","type":"journal-article","created":{"date-parts":[[2015,7,30]],"date-time":"2015-07-30T01:06:25Z","timestamp":1438218385000},"page":"800-801","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":4,"title":["Spinal and bulbar muscular atrophy and Charcot\u2013Marie\u2013Tooth type 1A: Co-existence of two rare neuromuscular genetic diseases in the same patient"],"prefix":"10.1016","volume":"25","author":[{"given":"Anna","family":"Sagnelli","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vidmer","family":"Scaioli","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Giuseppe","family":"Piscosquito","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ettore","family":"Salsano","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Eleonora","family":"Dalla Bella","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cinzia","family":"Gellera","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Davide","family":"Pareyson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.nmd.2015.07.015_bib0010","doi-asserted-by":"crossref","first-page":"3242","DOI":"10.1093\/brain\/awp258","article-title":"Clinical features of spinal and Bulbar Muscular Atrophy","volume":"132","author":"Rhodes","year":"2009","journal-title":"Brain"},{"key":"10.1016\/j.nmd.2015.07.015_bib0015","series-title":"Spinal and Bulbar Muscular Atrophy","author":"La Spada","year":"1999"},{"key":"10.1016\/j.nmd.2015.07.015_bib0020","doi-asserted-by":"crossref","first-page":"654","DOI":"10.1016\/S1474-4422(09)70110-3","article-title":"Diagnosis, natural history, and management of Charcot-Marie-Tooth disease","volume":"8","author":"Pareyson","year":"2009","journal-title":"Lancet Neurol"},{"key":"10.1016\/j.nmd.2015.07.015_bib0025","first-page":"873872","article-title":"Assessing function and endurance in adults with spinal and bulbar muscular atrophy: validity of the adult myopathy assessment tool","author":"Harris-Love","year":"2014","journal-title":"Rehabil Res Pract"},{"key":"10.1016\/j.nmd.2015.07.015_bib0030","doi-asserted-by":"crossref","first-page":"191","DOI":"10.1111\/j.1529-8027.2011.00350.x","article-title":"Reliability of the CMT neuropathy score (second version) in Charcot-Marie-Tooth disease","volume":"16","author":"Murphy","year":"2001","journal-title":"J Peripher Nerv Syst"},{"key":"10.1016\/j.nmd.2015.07.015_bib0035","doi-asserted-by":"crossref","first-page":"252","DOI":"10.1002\/(SICI)1097-4598(200002)23:2<252::AID-MUS17>3.0.CO;2-P","article-title":"Sensory involvement in spinal-bulbar muscular atrophy (Kennedy's disease)","volume":"23","author":"Antonini","year":"2000","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.nmd.2015.07.015_bib0040","doi-asserted-by":"crossref","first-page":"2063","DOI":"10.1002\/mds.22566","article-title":"Postural tremor in X-linked spinal and bulbar muscular atrophy","volume":"24","author":"Hanajima","year":"2009","journal-title":"Mov Disord"},{"key":"10.1016\/j.nmd.2015.07.015_bib0045","doi-asserted-by":"crossref","first-page":"265","DOI":"10.5334\/tohm.211","article-title":"Head and arm tremor in X-linked spinal and bulbar muscular atrophy","volume":"4","author":"Aicua","year":"2014","journal-title":"Tremor Other Hyperkinet Mov (N Y)"},{"key":"10.1016\/j.nmd.2015.07.015_bib0050","doi-asserted-by":"crossref","first-page":"145","DOI":"10.1002\/mus.24205","article-title":"Double-trouble in pediatric neurology: myotonia congenita combined with Charcot-Marie-Tooth disease type 1A","volume":"50","author":"Ardissone","year":"2014","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.nmd.2015.07.015_bib0055","doi-asserted-by":"crossref","first-page":"197","DOI":"10.1016\/j.jns.2009.09.028","article-title":"Combination of myotonic dystrophy and hereditary motor and sensory neuropathy","volume":"288","author":"Kurt","year":"2010","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.nmd.2015.07.015_bib0060","doi-asserted-by":"crossref","first-page":"818","DOI":"10.1002\/(SICI)1097-4598(200005)23:5<818::AID-MUS23>3.0.CO;2-O","article-title":"Becker muscular dystrophy combined with X-linked Charcot-Marie-Tooth neuropathy","volume":"23","author":"Bergmann","year":"2000","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.nmd.2015.07.015_bib0065","doi-asserted-by":"crossref","first-page":"92","DOI":"10.1186\/1471-2350-14-92","article-title":"Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A \u2013 evidence for \u201cdouble trouble\u201d overlapping syndromes","volume":"14","author":"Schreiber","year":"2013","journal-title":"BMC Med Genet"}],"container-title":["Neuromuscular Disorders"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0960896615006732?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0960896615006732?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,18]],"date-time":"2025-10-18T08:03:30Z","timestamp":1760774610000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0960896615006732"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,10]]},"references-count":12,"journal-issue":{"issue":"10","published-print":{"date-parts":[[2015,10]]}},"alternative-id":["S0960896615006732"],"URL":"https:\/\/doi.org\/10.1016\/j.nmd.2015.07.015","relation":{},"ISSN":["0960-8966"],"issn-type":[{"value":"0960-8966","type":"print"}],"subject":[],"published":{"date-parts":[[2015,10]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Spinal and bulbar muscular atrophy and Charcot\u2013Marie\u2013Tooth type 1A: Co-existence of two rare neuromuscular genetic diseases in the same patient","name":"articletitle","label":"Article Title"},{"value":"Neuromuscular Disorders","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.nmd.2015.07.015","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2015 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}