{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,21]],"date-time":"2026-10-21T12:41:00Z","timestamp":1792586460720,"version":"4.5.0"},"reference-count":22,"publisher":"Elsevier BV","issue":"11","license":[{"start":{"date-parts":[[2012,11,1]],"date-time":"2012-11-01T00:00:00Z","timestamp":1351728000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2012,11,1]],"date-time":"2012-11-01T00:00:00Z","timestamp":1351728000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"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":[[2012,11]]},"DOI":"10.1016\/j.nmd.2012.05.017","type":"journal-article","created":{"date-parts":[[2012,8,1]],"date-time":"2012-08-01T12:03:36Z","timestamp":1343822616000},"page":"974-979","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":65,"title":["Epidemiological surveillance of myotonic dystrophy type 1: A 25-year population-based study"],"prefix":"10.1016","volume":"22","author":[{"given":"Jean","family":"Mathieu","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Claude","family":"Pr\u00e9vost","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.nmd.2012.05.017_b0005","doi-asserted-by":"crossref","first-page":"545","DOI":"10.1038\/355545a0","article-title":"Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy","volume":"355","author":"Harley","year":"1992","journal-title":"Nature"},{"key":"10.1016\/j.nmd.2012.05.017_b0010","series-title":"Myotonic dystrophy","author":"Harper","year":"2001"},{"key":"10.1016\/j.nmd.2012.05.017_b0015","doi-asserted-by":"crossref","first-page":"839","DOI":"10.1212\/WNL.40.5.839","article-title":"Genealogical reconstruction of myotonic dystrophy in the Saguenay-Lac-Saint-Jean area (Quebec, Canada)","volume":"40","author":"Mathieu","year":"1990","journal-title":"Neurology"},{"key":"10.1016\/j.nmd.2012.05.017_b0020","doi-asserted-by":"crossref","first-page":"800","DOI":"10.1136\/jnnp.2006.107185","article-title":"Towards an integrative approach to the management of myotonic dystrophy type 1","volume":"78","author":"Gagnon","year":"2007","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"10.1016\/j.nmd.2012.05.017_b0025","doi-asserted-by":"crossref","first-page":"68","DOI":"10.1002\/ajmg.a.20560","article-title":"Psychosocial impact of predictive testing for myotonic dystrophy type 1","volume":"126A","author":"Pr\u00e9vost","year":"2004","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.nmd.2012.05.017_b0030","doi-asserted-by":"crossref","first-page":"420","DOI":"10.1212\/WNL.39.3.420","article-title":"Criteria for establishing the validity of genetic recombination in myotonic dystrophy","volume":"39","author":"Griggs","year":"1989","journal-title":"Neurology"},{"key":"10.1016\/j.nmd.2012.05.017_b0035","first-page":"1084","article-title":"Genetic risk for children of women with myotonic dystrophy","volume":"48","author":"Koch","year":"1991","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.nmd.2012.05.017_b0040","doi-asserted-by":"crossref","first-page":"336","DOI":"10.1212\/WNL.56.3.336","article-title":"Assessment of a disease-specific impairment rating scale in myotonic dystrophy","volume":"56","author":"Mathieu","year":"2001","journal-title":"Neurology"},{"key":"10.1016\/j.nmd.2012.05.017_b0045","doi-asserted-by":"crossref","first-page":"203","DOI":"10.1212\/WNL.42.1.203","article-title":"Myotonic dystrophy: clinical assessment of muscular disability in an isolated population with presumed homogeneous mutation","volume":"42","author":"Mathieu","year":"1992","journal-title":"Neurology"},{"key":"10.1016\/j.nmd.2012.05.017_b0050","doi-asserted-by":"crossref","first-page":"S7","DOI":"10.1212\/WNL.0b013e31820502f6","article-title":"Analysis of current multiple sclerosis registries","volume":"76","author":"Hurwitz","year":"2011","journal-title":"Neurology"},{"key":"10.1016\/j.nmd.2012.05.017_b0055","doi-asserted-by":"crossref","first-page":"234","DOI":"10.1111\/j.1399-0004.1992.tb03247.x","article-title":"Fertility in myotonic dystrophy in Saguenay-Lac-St-Jean: a historical perspective","volume":"42","author":"Dao","year":"1992","journal-title":"Clin Genet"},{"key":"10.1016\/j.nmd.2012.05.017_b0060","series-title":"Genetics, demography and health in minority populations","article-title":"Socio-cultural factors influencing the spread of myotonic dystrophy in the Saguenay-Lac-Saint-Jean region of the Province of Quebec (Canada)","author":"Veillette","year":"1991"},{"key":"10.1016\/j.nmd.2012.05.017_b0065","doi-asserted-by":"crossref","first-page":"856","DOI":"10.1136\/jmg.33.10.856","article-title":"Adverse psychological events occurring in the first year after predictive testing for Huntington\u2019s disease","volume":"33","author":"Lawson","year":"1996","journal-title":"J Med Genet"},{"key":"10.1016\/j.nmd.2012.05.017_b0070","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1002\/ajmg.1320480305","article-title":"Presymptomatic DNA testing for Huntington disease: identifying the need for psychological intervention","volume":"48","author":"Tibben","year":"1993","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.nmd.2012.05.017_b0075","doi-asserted-by":"crossref","first-page":"1006","DOI":"10.1002\/ajmg.1320430618","article-title":"Five years experience of predictive testing for myotonic dystrophy using linked DNA markers","volume":"43","author":"Reardon","year":"1992","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.nmd.2012.05.017_b0080","doi-asserted-by":"crossref","first-page":"1557","DOI":"10.1093\/brain\/121.8.1557","article-title":"Age and causes of death in adult-onset myotonic dystrophy","volume":"121","author":"De Die-Smulders","year":"1998","journal-title":"Brain"},{"key":"10.1016\/j.nmd.2012.05.017_b0085","doi-asserted-by":"crossref","first-page":"1658","DOI":"10.1212\/WNL.52.8.1658","article-title":"A ten-year study of mortality in a cohort of patients with myotonic dystrophy","volume":"52","author":"Mathieu","year":"1999","journal-title":"Neurology"},{"key":"10.1016\/j.nmd.2012.05.017_b0090","series-title":"Treasury of human inherance 4, part V","article-title":"Dystrophia myotonica and allied diseases","author":"Bell","year":"1947"},{"key":"10.1016\/j.nmd.2012.05.017_b0095","series-title":"Myotonia","author":"Thomasen","year":"1948"},{"issue":"Suppl.","key":"10.1016\/j.nmd.2012.05.017_b0100","first-page":"1","article-title":"La dystrophie myotonique (Steinert) et la myotonie cong\u00e9nitale (Thomsen) en Suisse","volume":"7","author":"Klein","year":"1958","journal-title":"J Genet Hum"},{"key":"10.1016\/j.nmd.2012.05.017_b0105","doi-asserted-by":"crossref","first-page":"648","DOI":"10.1002\/mus.21934","article-title":"Survival and CTG repeat expansion in adults with myotonic dystrophy type 1","volume":"43","author":"Groh","year":"2011","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.nmd.2012.05.017_b0110","doi-asserted-by":"crossref","first-page":"344","DOI":"10.1034\/j.1399-0004.2001.590508.x","article-title":"Epidemiology of myotonic dystrophy in Italy: re-appraisal after genetic diagnosis","volume":"59","author":"Siciliano","year":"2001","journal-title":"Clin Genet"}],"container-title":["Neuromuscular Disorders"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0960896612001824?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0960896612001824?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,18]],"date-time":"2025-10-18T08:01:01Z","timestamp":1760774461000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0960896612001824"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,11]]},"references-count":22,"journal-issue":{"issue":"11","published-print":{"date-parts":[[2012,11]]}},"alternative-id":["S0960896612001824"],"URL":"https:\/\/doi.org\/10.1016\/j.nmd.2012.05.017","relation":{},"ISSN":["0960-8966"],"issn-type":[{"value":"0960-8966","type":"print"}],"subject":[],"published":{"date-parts":[[2012,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Epidemiological surveillance of myotonic dystrophy type 1: A 25-year population-based study","name":"articletitle","label":"Article Title"},{"value":"Neuromuscular Disorders","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.nmd.2012.05.017","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2012 Published by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}