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Journal Abstract Search

238 related items for PubMed ID: 19506430

  • 1. 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
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  • 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 13; 68(7):522-4. PubMed ID: 17296918
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  • 3. Phenotypic features of myoclonus-dystonia in three kindreds.
    Doheny DO, Brin MF, Morrison CE, Smith CJ, Walker RH, Abbasi S, Müller B, Garrels J, Liu L, De Carvalho Aguiar P, Schilling K, Kramer P, De Leon D, Raymond D, Saunders-Pullman R, Klein C, Bressman SB, Schmand B, Tijssen MA, Ozelius LJ, Silverman JM.
    Neurology; 2002 Oct 22; 59(8):1187-96. PubMed ID: 12391346
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  • 4. Abnormal low frequency drive in myoclonus-dystonia patients correlates with presence of dystonia.
    Foncke EM, Bour LJ, van der Meer JN, Koelman JH, Tijssen MA.
    Mov Disord; 2007 Jul 15; 22(9):1299-307. PubMed ID: 17486590
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  • 6. 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, French Dystonia Network.
    J Med Genet; 2006 May 15; 43(5):394-400. PubMed ID: 16227522
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  • 7. Distal myoclonus and late onset in a large Dutch family with myoclonus-dystonia.
    Foncke EM, Gerrits MC, van Ruissen F, Baas F, Hedrich K, Tijssen CC, Klein C, Tijssen MA.
    Neurology; 2006 Nov 14; 67(9):1677-80. PubMed ID: 17101905
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  • 9. Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependence.
    Saunders-Pullman R, Shriberg J, Heiman G, Raymond D, Wendt K, Kramer P, Schilling K, Kurlan R, Klein C, Ozelius LJ, Risch NJ, Bressman SB.
    Neurology; 2002 Jan 22; 58(2):242-5. PubMed ID: 11805251
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  • 10. 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 22; 13(2):178-80. PubMed ID: 18571946
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  • 11. 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 22; 130(Pt 10):2736-45. PubMed ID: 17898012
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  • 12. Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome.
    Zimprich A, Grabowski M, Asmus F, Naumann M, Berg D, Bertram M, Scheidtmann K, Kern P, Winkelmann J, Müller-Myhsok B, Riedel L, Bauer M, Müller T, Castro M, Meitinger T, Strom TM, Gasser T.
    Nat Genet; 2001 Sep 22; 29(1):66-9. PubMed ID: 11528394
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  • 13. 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 22; 19(12):1456-9. PubMed ID: 15389977
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  • 15. Cortical excitability in DYT-11 positive myoclonus dystonia.
    Sabine MeunierINSERM, U731, Paris, France., George Lourenco, Roze E, Apartis E, Trocello JM, Marie Vidailhet.
    Mov Disord; 2008 Apr 15; 23(5):761-4. PubMed ID: 18265016
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  • 16. Fear of harm, a possible phenotype of pediatric bipolar disorder: a dimensional approach to diagnosis for genotyping psychiatric syndromes.
    Papolos D, Mattis S, Golshan S, Molay F.
    J Affect Disord; 2009 Nov 15; 118(1-3):28-38. PubMed ID: 19631388
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  • 19. Myoclonus-dystonia: significance of large SGCE deletions.
    Grünewald A, Djarmati A, Lohmann-Hedrich K, Farrell K, Zeller JA, Allert N, Papengut F, Petersen B, Fung V, Sue CM, O'Sullivan D, Mahant N, Kupsch A, Chuang RS, Wiegers K, Pawlack H, Hagenah J, Ozelius LJ, Stephani U, Schuit R, Lang AE, Volkmann J, Münchau A, Klein C.
    Hum Mutat; 2008 Feb 15; 29(2):331-2. PubMed ID: 18205193
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  • 20. Obsessive-compulsive disorder and executive deficits in two patients with primary dystonia.
    Bugalho P, Correa B, Guimarães J, Xavier M.
    Parkinsonism Relat Disord; 2006 Sep 15; 12(6):388-91. PubMed ID: 16731024
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