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 *

299 related articles for article (PubMed ID: 16534121)

  • 1. Phenotype-genotype correlation in Dutch patients with myoclonus-dystonia.
    Gerrits MC; Foncke EM; de Haan R; Hedrich K; van de Leemput YL; Baas F; Ozelius LJ; Speelman JD; Klein C; Tijssen MA
    Neurology; 2006 Mar; 66(5):759-61. PubMed ID: 16534121
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriers.
    Hess CW; Raymond D; Aguiar Pde C; Frucht S; Shriberg J; Heiman GA; Kurlan R; Klein C; Bressman SB; Ozelius LJ; Saunders-Pullman R
    Neurology; 2007 Feb; 68(7):522-4. PubMed ID: 17296918
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes.
    Tezenas du Montcel S; Clot F; Vidailhet M; Roze E; Damier P; Jedynak CP; Camuzat A; Lagueny A; Vercueil L; Doummar D; Guyant-Maréchal L; Houeto JL; Ponsot G; Thobois S; Cournelle MA; Durr A; Durif F; Echenne B; Hannequin D; Tranchant C; Brice A;
    J Med Genet; 2006 May; 43(5):394-400. PubMed ID: 16227522
    [TBL] [Abstract][Full Text] [Related]  

  • 4. "Jerky" dystonia in children: spectrum of phenotypes and genetic testing.
    Asmus F; Langseth A; Doherty E; Nestor T; Munz M; Gasser T; Lynch T; King MD
    Mov Disord; 2009 Apr; 24(5):702-9. PubMed ID: 19117362
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystonias.
    Grundmann K; Laubis-Herrmann U; Dressler D; Vollmer-Haase J; Bauer P; Stuhrmann M; Schulte T; Schöls L; Topka H; Riess O
    Mov Disord; 2004 Nov; 19(11):1294-7. PubMed ID: 15390016
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel mutation of the epsilon-sarcoglycan gene in a Chinese family with myoclonus-dystonia syndrome.
    Chen XP; Zhang YW; Zhang SS; Chen Q; Burgunder JM; Wu SH; Yang Y; Luo ZM; Shang HF
    Mov Disord; 2008 Jul; 23(10):1472-5. PubMed ID: 18581468
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with epsilon-sarcoglycan mutations.
    Raymond D; Saunders-Pullman R; de Carvalho Aguiar P; Schule B; Kock N; Friedman J; Harris J; Ford B; Frucht S; Heiman GA; Jennings D; Doheny D; Brin MF; de Leon Brin D; Multhaupt-Buell T; Lang AE; Kurlan R; Klein C; Ozelius L; Bressman S
    Mov Disord; 2008 Mar; 23(4):588-92. PubMed ID: 18175340
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The epsilon-sarcoglycan gene in myoclonic syndromes.
    Valente EM; Edwards MJ; Mir P; DiGiorgio A; Salvi S; Davis M; Russo N; Bozi M; Kim HT; Pennisi G; Quinn N; Dallapiccola B; Bhatia KP
    Neurology; 2005 Feb; 64(4):737-9. PubMed ID: 15728306
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inherited myoclonus-dystonia and epilepsy: further evidence of an association?
    O'Riordan S; Ozelius LJ; de Carvalho Aguiar P; Hutchinson M; King M; Lynch T
    Mov Disord; 2004 Dec; 19(12):1456-9. PubMed ID: 15389977
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genomic deletion size at the epsilon-sarcoglycan locus determines the clinical phenotype.
    Asmus F; Hjermind LE; Dupont E; Wagenstaller J; Haberlandt E; Munz M; Strom TM; Gasser T
    Brain; 2007 Oct; 130(Pt 10):2736-45. PubMed ID: 17898012
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Myoclonus-dystonia syndrome: clinical presentation, disease course, and genetic features in 11 families.
    Nardocci N; Zorzi G; Barzaghi C; Zibordi F; Ciano C; Ghezzi D; Garavaglia B
    Mov Disord; 2008 Jan; 23(1):28-34. PubMed ID: 17853490
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype.
    Asmus F; Zimprich A; Tezenas Du Montcel S; Kabus C; Deuschl G; Kupsch A; Ziemann U; Castro M; Kühn AA; Strom TM; Vidailhet M; Bhatia KP; Dürr A; Wood NW; Brice A; Gasser T
    Ann Neurol; 2002 Oct; 52(4):489-92. PubMed ID: 12325078
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Large deletions account for an increasing number of mutations in SGCE.
    Han F; Racacho L; Yang H; Read T; Suchowersky O; Lang AE; Grimes DA; Bulman DE
    Mov Disord; 2008 Feb; 23(3):456-60. PubMed ID: 18098280
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia.
    Asmus F; Devlin A; Munz M; Zimprich A; Gasser T; Chinnery PF
    Mov Disord; 2007 Oct; 22(14):2104-9. PubMed ID: 17702043
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel and de novo mutations of the SGCE gene in Brazilian patients with myoclonus-dystonia.
    Borges V; Aguiar Pde C; Ferraz HB; Ozelius LJ
    Mov Disord; 2007 Jun; 22(8):1208-9. PubMed ID: 17394244
    [No Abstract]   [Full Text] [Related]  

  • 16. Pediatric writer's cramp in myoclonus-dystonia: maternal imprinting hides positive family history.
    Gerrits MC; Foncke EM; Koelman JH; Tijssen MA
    Eur J Paediatr Neurol; 2009 Mar; 13(2):178-80. PubMed ID: 18571946
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Unusual familial presentation of epsilon-sarcoglycan gene mutation with falls and writer's cramp.
    Koukouni V; Valente EM; Cordivari C; Bhatia KP; Quinn NP
    Mov Disord; 2008 Oct; 23(13):1913-5. PubMed ID: 18702114
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Myoclonus-dystonia due to genomic deletions in the epsilon-sarcoglycan gene.
    Asmus F; Salih F; Hjermind LE; Ostergaard K; Munz M; Kühn AA; Dupont E; Kupsch A; Gasser T
    Ann Neurol; 2005 Nov; 58(5):792-7. PubMed ID: 16240355
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary myoclonus dystonia (DYT11): a novel SGCE gene mutation with intrafamilial phenotypic heterogeneity.
    Wong SH; Steiger MJ; Larner AJ; Fletcher NA
    Mov Disord; 2010 May; 25(7):956-7. PubMed ID: 20222131
    [No Abstract]   [Full Text] [Related]  

  • 20. Is psychopathology part of the phenotypic spectrum of myoclonus-dystonia?: a study of a large Dutch M-D family.
    Foncke EM; Cath D; Zwinderman K; Smit J; Schmand B; Tijssen M
    Cogn Behav Neurol; 2009 Jun; 22(2):127-33. PubMed ID: 19506430
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.