These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 8723633)

  • 1. [Genetic study of idiopathic torsion dystonia in Russia].
    Dadali EL; Markova ED; Petrin AN; Ivanova-Smolenskaia IA; Okuneva EG
    Genetika; 1996 Mar; 32(3):415-9. PubMed ID: 8723633
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The genetics of idiopathic torsion dystonia.
    Fahn S
    Int J Neurol; 1991-1992; 25-26():70-80. PubMed ID: 11980065
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Evidence for locus heterogeneity in autosomal dominant torsion dystonia.
    Ahmad F; Davis MB; Waddy HM; Oley CA; Marsden CD; Harding AE
    Genomics; 1993 Jan; 15(1):9-12. PubMed ID: 8432555
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Intrafamilial correlation in idiopathic torsion dystonia.
    Fletcher NA; Harding AE; Marsden CD
    Mov Disord; 1991; 6(4):310-4. PubMed ID: 1758449
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetics, geography and intelligence in the torsion dystonias.
    Eldridge R; Edgar A; Cooper IS
    Birth Defects Orig Artic Ser; 1971 Feb; 7(1):167-77. PubMed ID: 5173357
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of the clinical course of non-Jewish, autosomal dominant torsion dystonia.
    Burke RE; Brin MF; Fahn S; Bressman SB; Moskowitz C
    Mov Disord; 1986; 1(3):163-78. PubMed ID: 3504242
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Exclusion of the DYT1 locus in familial torticollis.
    Bressman SB; Warner TT; Almasy L; Uitti RJ; Greene PE; Heiman GA; Raymond D; Ford B; de Leon D; Fahn S; Kramer PL; Risch NJ; Maraganore DM; Nygaard TG; Harding AE
    Ann Neurol; 1996 Oct; 40(4):681-4. PubMed ID: 8871591
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite families.
    Almasy L; Bressman SB; Raymond D; Kramer PL; Greene PE; Heiman GA; Ford B; Yount J; de Leon D; Chouinard S; Saunders-Pullman R; Brin MF; Kapoor RP; Jones AC; Shen H; Fahn S; Risch NJ; Nygaard TG
    Ann Neurol; 1997 Oct; 42(4):670-3. PubMed ID: 9382482
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Characteristics of the clinical course, pathogenesis and treatment of torsion dystonia in childhood].
    Markova ED
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(8):32-5. PubMed ID: 2588895
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34.
    Kramer PL; de Leon D; Ozelius L; Risch N; Bressman SB; Brin MF; Schuback DE; Burke RE; Kwiatkowski DJ; Shale H
    Ann Neurol; 1990 Feb; 27(2):114-20. PubMed ID: 2317008
    [TBL] [Abstract][Full Text] [Related]  

  • 12. X-linked recessive torsion dystonia in the Philippines.
    Kupke KG; Lee LV; Viterbo GH; Arancillo J; Donlon T; Müller U
    Am J Med Genet; 1990 Jun; 36(2):237-42. PubMed ID: 2368812
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 50():45-56. PubMed ID: 3400502
    [TBL] [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; 12(6):1000-6. PubMed ID: 9399227
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene.
    Defazio G; Brancati F; Valente EM; Caputo V; Pizzuti A; Martino D; Abbruzzese G; Livrea P; Berardelli A; Dallapiccola B
    Mov Disord; 2003 Feb; 18(2):207-12. PubMed ID: 12539217
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Linkage analysis with chromosome 9 markers in hereditary essential tremor.
    Conway D; Bain PG; Warner TT; Davis MB; Findley LJ; Thompson PD; Marsden CD; Harding AE
    Mov Disord; 1993 Jul; 8(3):374-6. PubMed ID: 8341306
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Early onset periodontitis: a comparison and evaluation of two proposed modes of inheritance.
    Long JC; Nance WE; Waring P; Burmeister JA; Ranney RR
    Genet Epidemiol; 1987; 4(1):13-24. PubMed ID: 3569875
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Torsion dystonia in Israel.
    Korczyn AD; Kahana E; Zilber N; Streifler M; Carasso R; Alter M
    Ann Neurol; 1980 Oct; 8(4):387-91. PubMed ID: 7436383
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mendelian inheritance of isolated nonsyndromic cleft palate.
    Rollnick BR; Kaye CI
    Am J Med Genet; 1986 Jul; 24(3):465-73. PubMed ID: 3728565
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South Tyrol.
    Klein C; Pramstaller PP; Castellan CC; Breakefield XO; Kramer PL; Ozelius LJ
    Ann Neurol; 1998 Sep; 44(3):394-8. PubMed ID: 9749609
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.