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 *

124 related articles for article (PubMed ID: 21370267)

  • 1. A new familial syndrome with dystonia and lower limb action myoclonus.
    Groen J; van Rootselaar AF; van der Salm SM; Bloem BR; Tijssen M
    Mov Disord; 2011 Apr; 26(5):896-900. PubMed ID: 21370267
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Myoclonus-dystonia: an update.
    Kinugawa K; Vidailhet M; Clot F; Apartis E; Grabli D; Roze E
    Mov Disord; 2009 Mar; 24(4):479-89. PubMed ID: 19117361
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Responsiveness to levodopa in epsilon-sarcoglycan deletions.
    Luciano MS; Ozelius L; Sims K; Raymond D; Liu L; Saunders-Pullman R
    Mov Disord; 2009 Feb; 24(3):425-8. PubMed ID: 19133653
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Myoclonus-dystonia and spinocerebellar ataxia type 14 presenting with similar phenotypes: trunk tremor, myoclonus, and dystonia.
    Foncke EM; Beukers RJ; Tijssen CC; Koelman JH; Tijssen MA
    Parkinsonism Relat Disord; 2010 May; 16(4):288-9. PubMed ID: 19913450
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Hereditary myoclonic dystonia, hereditary torsion dystonia and hereditary essential myoclonus: an area of confusion.
    Quinn NP; Rothwell JC; Thompson PD; Marsden CD
    Adv Neurol; 1988; 50():391-401. PubMed ID: 3400498
    [No Abstract]   [Full Text] [Related]  

  • 11. Electrophysiological features of myoclonus-dystonia.
    Li JY; Cunic DI; Paradiso G; Gunraj C; Pal PK; Lang AE; Chen R
    Mov Disord; 2008 Oct; 23(14):2055-61. PubMed ID: 18759341
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutations.
    Roze E; Apartis E; Clot F; Dorison N; Thobois S; Guyant-Marechal L; Tranchant C; Damier P; Doummar D; Bahi-Buisson N; André-Obadia N; Maltete D; Echaniz-Laguna A; Pereon Y; Beaugendre Y; Dupont S; De Greslan T; Jedynak CP; Ponsot G; Dussaule JC; Brice A; Dürr A; Vidailhet M
    Neurology; 2008 Mar; 70(13):1010-6. PubMed ID: 18362280
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. Clinical reasoning: A 13-year-old boy presenting with dystonia, myoclonus, and anxiety.
    Blackburn JS; Cirillo ML
    Neurology; 2012 Mar; 78(11):e72-6. PubMed ID: 22411962
    [No Abstract]   [Full Text] [Related]  

  • 17. "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]  

  • 18. 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]  

  • 19. A neurophysiological study of myoclonus in patients with DYT11 myoclonus-dystonia syndrome.
    Marelli C; Canafoglia L; Zibordi F; Ciano C; Visani E; Zorzi G; Garavaglia B; Barzaghi C; Albanese A; Soliveri P; Leone M; Panzica F; Scaioli V; Pincherle A; Nardocci N; Franceschetti S
    Mov Disord; 2008 Oct; 23(14):2041-8. PubMed ID: 18759336
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Expanding the phenomenology of benign hereditary chorea: evolution from chorea to myoclonus and dystonia.
    Armstrong MJ; Shah BB; Chen R; Angel MJ; Lang AE
    Mov Disord; 2011 Oct; 26(12):2296-7. PubMed ID: 21714005
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.