{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,20]],"date-time":"2025-10-20T17:07:42Z","timestamp":1760980062544},"reference-count":13,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2004,10,7]],"date-time":"2004-10-07T00:00:00Z","timestamp":1097107200000},"content-version":"vor","delay-in-days":8772,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Annals of Neurology"],"published-print":{"date-parts":[[1980,10]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>A country\u2010wide search for idiopathic torsion dystonia (ITD) in Israel between 1969 and 1975 revealed 42 patients (41 Jewish and 1 Druze Arab). Prevalence of ITD per million population, age\u2010adjusted to the United States population in 1970, was 10.8 in the total Jewish population (22.0 among Jews of European extraction contrasted with 1.5 among Jews with Afro\u2010Asian forebears). Among Europeans, the highest prevalence was among Jews from Eastern Europe.<\/jats:p><jats:p>The average age\u2010adjusted annual incidence rates per million population were 0.43 in the total Jewish population, 0.98 in the Europeans, and 0.11 in the Afro\u2010Asians. Among the 40 patients for whom familial data were available, the majority of cases (26) were sporadic. The other 14 belonged to four unrelated European families, all of Russian\u2010Polish origin. The pattern of inheritance in these four families fits an autosomal dominant model with incomplete penetrance.<\/jats:p>","DOI":"10.1002\/ana.410080409","type":"journal-article","created":{"date-parts":[[2005,1,1]],"date-time":"2005-01-01T13:15:30Z","timestamp":1104585330000},"page":"387-391","source":"Crossref","is-referenced-by-count":32,"title":["Torsion dystonia in israel"],"prefix":"10.1002","volume":"8","author":[{"given":"Amos D.","family":"Korczyn","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Esther","family":"Kahana","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nelly","family":"Zilber","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Max","family":"Streifler","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Raphael","family":"Carasso","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Milton","family":"Alter","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2004,10,7]]},"reference":[{"key":"e_1_2_1_2_2","first-page":"115","article-title":"Differences in torsion dystonia among Israeli ethnic groups","volume":"14","author":"Alter M","year":"1975","journal-title":"Adv Neurol"},{"key":"e_1_2_1_3_2","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.20.11_Part_2.1"},{"key":"e_1_2_1_4_2","first-page":"457","article-title":"The primary hereditary dystonias","volume":"14","author":"Eldridge R","year":"1976","journal-title":"Adv Neurol"},{"key":"e_1_2_1_5_2","first-page":"248","article-title":"The hereditary torsion dystonias (dystonia musculorum deformans): geographical distribution and IQ in dominant and recessive forms","volume":"94","author":"Eldridge R","year":"1969","journal-title":"Trans Am Neurol Assoc"},{"key":"e_1_2_1_6_2","first-page":"27","article-title":"The torsion dystonias: some genetic and psychiatric implications","volume":"3","author":"Eldridge R","year":"1971","journal-title":"Psychiatr Forum"},{"key":"e_1_2_1_7_2","volume-title":"General Population Characteristics, U.S. Summary, U.S. Department of Commerce, Bureau of the Census","year":"1970"},{"key":"e_1_2_1_8_2","first-page":"121","article-title":"Dystonia in the Black and Puerto Rican population","volume":"14","author":"Golden GS","year":"1976","journal-title":"Adv Neurol"},{"key":"e_1_2_1_9_2","first-page":"205","article-title":"Various genetic traits and diseases among the Jewish ethnic groups","volume":"10","author":"Goodman RM","year":"1974","journal-title":"Birth Defects"},{"key":"e_1_2_1_10_2","doi-asserted-by":"publisher","DOI":"10.1001\/archneurpsyc.1944.02290280003001"},{"key":"e_1_2_1_11_2","doi-asserted-by":"publisher","DOI":"10.1007\/BF01675314"},{"key":"e_1_2_1_12_2","doi-asserted-by":"publisher","DOI":"10.1016\/B978-1-4832-8363-0.50501-2"},{"key":"e_1_2_1_13_2","first-page":"290","article-title":"Serum levels of dopamine\u2010beta\u2010hydroxlase in dystonia","volume":"15","author":"Rabinowitz R","year":"1979","journal-title":"Isr J Med Sci"},{"key":"e_1_2_1_14_2","volume-title":"Central Bureau of Statistics","year":"1969"}],"container-title":["Annals of Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fana.410080409","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ana.410080409","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,7]],"date-time":"2023-10-07T20:19:02Z","timestamp":1696709942000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ana.410080409"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1980,10]]},"references-count":13,"journal-issue":{"issue":"4","published-print":{"date-parts":[[1980,10]]}},"alternative-id":["10.1002\/ana.410080409"],"URL":"https:\/\/doi.org\/10.1002\/ana.410080409","archive":["Portico"],"relation":{},"ISSN":["0364-5134","1531-8249"],"issn-type":[{"value":"0364-5134","type":"print"},{"value":"1531-8249","type":"electronic"}],"subject":[],"published":{"date-parts":[[1980,10]]}}}