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Journal Abstract Search
278 related items for PubMed ID: 11980065
1. The genetics of idiopathic torsion dystonia. Fahn S. Int J Neurol; ; 25-26():70-80. PubMed ID: 11980065 [Abstract] [Full Text] [Related]
6. Exclusion of the DYT1 locus in a non-Jewish family with early-onset dystonia. Bressman SB, Hunt AL, Heiman GA, Brin MF, Burke RE, Fahn S, Trugman JM, de Leon D, Kramer PL, Wilhelmsen KC. Mov Disord; 1994 Nov; 9(6):626-32. PubMed ID: 7845403 [Abstract] [Full Text] [Related]
10. Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritance. Bressman SB, de Leon D, Brin MF, Risch N, Burke RE, Greene PE, Shale H, Fahn S. Ann Neurol; 1989 Nov; 26(5):612-20. PubMed ID: 2817837 [Abstract] [Full Text] [Related]
11. Inheritance of idiopathic torsion dystonia among Ashkenazi Jews. Bressman SB, de Leon D, Brin MF, Risch N, Shale H, Burke RE, Greene PE, Fahn S. Adv Neurol; 1988 Nov; 50():45-56. PubMed ID: 3400502 [Abstract] [Full Text] [Related]
13. A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia. Slominsky PA, Markova ED, Shadrina MI, Illarioshkin SN, Miklina NI, Limborska SA, Ivanova-Smolenskaya IA. Hum Mutat; 1999 Sep 19; 14(3):269. PubMed ID: 10477437 [Abstract] [Full Text] [Related]
14. Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family. Leube B, Kessler KR, Goecke T, Auburger G, Benecke R. Mov Disord; 1997 Nov 19; 12(6):1000-6. PubMed ID: 9399227 [Abstract] [Full Text] [Related]
15. Haplotype analysis at the DYT1 locus in Ashkenazi Jewish patients with occupational hand dystonia. Gasser T, Bove CM, Ozelius LJ, Hallett M, Charness ME, Hochberg FH, Breakefield XO. Mov Disord; 1996 Mar 19; 11(2):163-6. PubMed ID: 8684386 [Abstract] [Full Text] [Related]
16. Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance. Risch NJ, Bressman SB, deLeon D, Brin MF, Burke RE, Greene PE, Shale H, Claus EB, Cupples LA, Fahn S. Am J Hum Genet; 1990 Mar 19; 46(3):533-8. PubMed ID: 2309703 [Abstract] [Full Text] [Related]