{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,31]],"date-time":"2025-10-31T16:49:25Z","timestamp":1761929365488},"reference-count":17,"publisher":"Elsevier BV","issue":"1-2","license":[{"start":{"date-parts":[[2008,4,1]],"date-time":"2008-04-01T00:00:00Z","timestamp":1207008000000},"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":["Journal of the Neurological Sciences"],"published-print":{"date-parts":[[2008,4]]},"DOI":"10.1016\/j.jns.2007.10.006","type":"journal-article","created":{"date-parts":[[2007,12,5]],"date-time":"2007-12-05T18:31:01Z","timestamp":1196879461000},"page":"125-128","source":"Crossref","is-referenced-by-count":7,"title":["A comparison of the lengths of androgen receptor triplet repeats in brain and blood in motor neuron diseases"],"prefix":"10.1016","volume":"267","author":[{"given":"Rebecca B.","family":"Saunderson","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bing","family":"Yu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ronald J.A.","family":"Trent","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Roger","family":"Pamphlett","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.jns.2007.10.006_bib1","doi-asserted-by":"crossref","first-page":"301","DOI":"10.1038\/ng1292-301","article-title":"Meiotic stability and genotype\u2013phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy","volume":"2","author":"La Spada","year":"1992","journal-title":"Nat Genet"},{"key":"10.1016\/j.jns.2007.10.006_bib2","doi-asserted-by":"crossref","first-page":"1442","DOI":"10.1212\/WNL.51.5.1442","article-title":"Larger CAG expansions in skeletal muscle compared with lymphocytes in Kennedy disease but not in Huntington disease","volume":"51","author":"Ansved","year":"1998","journal-title":"Neurology"},{"key":"10.1016\/j.jns.2007.10.006_bib3","doi-asserted-by":"crossref","first-page":"568","DOI":"10.1212\/WNL.49.2.568","article-title":"Spinobulbar muscular atrophy can mimic ALS: the importance of genetic testing in male patients with atypical ALS","volume":"49","author":"Parboosingh","year":"1997","journal-title":"Neurology"},{"key":"10.1016\/j.jns.2007.10.006_bib4","doi-asserted-by":"crossref","first-page":"679","DOI":"10.1016\/j.mehy.2003.11.023","article-title":"Somatic mutation: a cause of sporadic neurodegenerative diseases?","volume":"62","author":"Pamphlett","year":"2004","journal-title":"Med Hypotheses"},{"key":"10.1016\/j.jns.2007.10.006_bib5","doi-asserted-by":"crossref","first-page":"77","DOI":"10.1038\/352077a0","article-title":"Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy","volume":"352","author":"La Spada","year":"1991","journal-title":"Nature"},{"key":"10.1016\/j.jns.2007.10.006_bib6","doi-asserted-by":"crossref","first-page":"1252","DOI":"10.1212\/01.WNL.0000058901.75728.4E","article-title":"Corticospinal tract degeneration in the progressive muscular atrophy variant of ALS","volume":"60","author":"Ince","year":"2003","journal-title":"Neurology"},{"key":"10.1016\/j.jns.2007.10.006_bib7","doi-asserted-by":"crossref","first-page":"1921","DOI":"10.1001\/archneur.59.12.1921","article-title":"X-linked bulbospinal neuronopathy: Kennedy disease","volume":"59","author":"Sperfeld","year":"2002","journal-title":"Arch Neurol"},{"key":"10.1016\/j.jns.2007.10.006_bib8","doi-asserted-by":"crossref","first-page":"262","DOI":"10.1016\/j.clinph.2006.10.006","article-title":"Upper motor neuron involvement in X-linked recessive bulbospinal muscular atrophy","volume":"118","author":"Pachatz","year":"2007","journal-title":"Clin Neurophysiol"},{"key":"10.1016\/j.jns.2007.10.006_bib9","doi-asserted-by":"crossref","first-page":"252","DOI":"10.1212\/WNL.51.1.252","article-title":"Kennedy's disease: unusual molecular pathologic and clinical features","volume":"51","author":"Shaw","year":"1998","journal-title":"Neurology"},{"key":"10.1016\/j.jns.2007.10.006_bib10","doi-asserted-by":"crossref","first-page":"4406","DOI":"10.1210\/jc.86.9.4406","article-title":"Pharmacogenetic polymorphisms of the AR and metabolism and susceptibility to hormone-induced azoospermia","volume":"86","author":"Yu","year":"2001","journal-title":"J Clin Endocrinol Metab"},{"key":"10.1016\/j.jns.2007.10.006_bib11","doi-asserted-by":"crossref","first-page":"748","DOI":"10.1038\/nrg906","article-title":"Mechanisms and consequences of somatic mosaicism in humans","volume":"3","author":"Youssoufian","year":"2002","journal-title":"Nat Rev Genet"},{"key":"10.1016\/j.jns.2007.10.006_bib12","doi-asserted-by":"crossref","first-page":"1397","DOI":"10.1093\/hmg\/2.9.1397","article-title":"Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy","volume":"2","author":"Anvret","year":"1993","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.jns.2007.10.006_bib13","doi-asserted-by":"crossref","first-page":"409","DOI":"10.1038\/ng0494-409","article-title":"Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm","volume":"6","author":"Telenius","year":"1994","journal-title":"Nat Genet"},{"key":"10.1016\/j.jns.2007.10.006_bib14","doi-asserted-by":"crossref","first-page":"856","DOI":"10.1007\/s004150170069","article-title":"Clinical features and skewed X-chromosome inactivation in female carriers of X-linked recessive spinal and bulbar muscular atrophy","volume":"248","author":"Ishihara","year":"2001","journal-title":"J Neurol"},{"key":"10.1016\/j.jns.2007.10.006_bib15","doi-asserted-by":"crossref","first-page":"452","DOI":"10.1007\/s004390000400","article-title":"Differential somatic CAG repeat instability in variable brain cell lineage in dentatorubral pallidoluysian atrophy (DRPLA): a laser-captured microdissection (LCM)-based analysis","volume":"107","author":"Watanabe","year":"2000","journal-title":"Hum Genet"},{"key":"10.1016\/j.jns.2007.10.006_bib16","doi-asserted-by":"crossref","first-page":"87","DOI":"10.1016\/S0022-510X(01)00596-2","article-title":"Single cell analysis of CAG repeat in brains of dentatorubral-pallidoluysian atrophy (DRPLA)","volume":"190","author":"Hashida","year":"2001","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.jns.2007.10.006_bib17","doi-asserted-by":"crossref","first-page":"2289","DOI":"10.1093\/brain\/123.11.2289","article-title":"Extramotor involvement in ALS: PET studies with the GABA(A) ligand [(11)C] flumazenil","volume":"123","author":"Lloyd","year":"2000","journal-title":"Brain"}],"container-title":["Journal of the Neurological Sciences"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022510X07007083?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022510X07007083?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,1,2]],"date-time":"2019-01-02T03:25:03Z","timestamp":1546399503000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0022510X07007083"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,4]]},"references-count":17,"journal-issue":{"issue":"1-2","published-print":{"date-parts":[[2008,4]]}},"alternative-id":["S0022510X07007083"],"URL":"https:\/\/doi.org\/10.1016\/j.jns.2007.10.006","relation":{},"ISSN":["0022-510X"],"issn-type":[{"value":"0022-510X","type":"print"}],"subject":[],"published":{"date-parts":[[2008,4]]}}}