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Journal Abstract Search

473 related items for PubMed ID: 19913450

  • 1. 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
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  • 2. 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 May; 50():391-401. PubMed ID: 3400498
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  • 5. 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 15; 25(7):956-7. PubMed ID: 20222131
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  • 7. New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14.
    Klebe S, Durr A, Rentschler A, Hahn-Barma V, Abele M, Bouslam N, Schöls L, Jedynak P, Forlani S, Denis E, Dussert C, Agid Y, Bauer P, Globas C, Wüllner U, Brice A, Riess O, Stevanin G.
    Ann Neurol; 2005 Nov 15; 58(5):720-9. PubMed ID: 16193476
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  • 9. Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings With Autosomal Recessive Spinocerebellar Ataxia Type 16.
    Kawarai T, Miyamoto R, Shimatani Y, Orlacchio A, Kaji R.
    JAMA Neurol; 2016 Jul 01; 73(7):888-90. PubMed ID: 27182963
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  • 10. Tremor and idiopathic dystonia.
    Jedynak CP, Bonnet AM, Agid Y.
    Mov Disord; 1991 Jul 01; 6(3):230-6. PubMed ID: 1922128
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  • 11. Slowly progressive cerebellar ataxia and cervical dystonia: clinical presentation of a new form of spinocerebellar ataxia?
    Kuoppamäki M, Giunti P, Quinn N, Wood NW, Bhatia KP.
    Mov Disord; 2003 Feb 01; 18(2):200-6. PubMed ID: 12539216
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  • 12. 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 01; 19(12):1456-9. PubMed ID: 15389977
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  • 13. The pleiotropic movement disorders phenotype of adult ataxia-telangiectasia.
    Méneret A, Ahmar-Beaugendre Y, Rieunier G, Mahlaoui N, Gaymard B, Apartis E, Tranchant C, Rivaud-Péchoux S, Degos B, Benyahia B, Suarez F, Maisonobe T, Koenig M, Durr A, Stern MH, Dubois d'Enghien C, Fischer A, Vidailhet M, Stoppa-Lyonnet D, Grabli D, Anheim M.
    Neurology; 2014 Sep 16; 83(12):1087-95. PubMed ID: 25122203
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  • 14. 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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  • 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 14; 23(1):28-34. PubMed ID: 17853490
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  • 16. Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia.
    Klein C, Gurvich N, Sena-Esteves M, Bressman S, Brin MF, Ebersole BJ, Fink S, Forsgren L, Friedman J, Grimes D, Holmgren G, Kyllerman M, Lang AE, de Leon D, Leung J, Prioleau C, Raymond D, Sanner G, Saunders-Pullman R, Vieregge P, Wahlström J, Breakefield XO, Kramer PL, Ozelius LJ, Sealfon SC.
    Ann Neurol; 2000 Mar 14; 47(3):369-73. PubMed ID: 10716258
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  • 17. 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 14; 66(5):759-61. PubMed ID: 16534121
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  • 19. 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 15; 23(4):588-92. PubMed ID: 18175340
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