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Journal Abstract Search

362 related items for PubMed ID: 9805989

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  • 5. Familial cortical myoclonic tremor with epilepsy (FCMTE): Clinical characteristics and exclusion of linkages to 8q and 2p in a large French family.
    Magnin E, Vidailhet M, Depienne C, Saint-Martin C, Bouteiller D, LeGuern E, Apartis E, Rumbach L, Labauge P.
    Rev Neurol (Paris); 2009 Oct; 165(10):812-20. PubMed ID: 19616813
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  • 7. [A case of familial essential myoclonus--electrophysiological study].
    Araki K, Kono I, Ueda Y, Kashima K, Shibasaki H.
    Rinsho Shinkeigaku; 1991 Aug; 31(8):864-8. PubMed ID: 1764862
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  • 17. Clinical analysis in familial cortical myoclonic tremor allows differential diagnosis with essential tremor.
    Bourdain F, Apartis E, Trocello JM, Vidal JS, Masnou P, Vercueil L, Vidailhet M.
    Mov Disord; 2006 May; 21(5):599-608. PubMed ID: 16281296
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  • 18. Rhythmic cortical myoclonus in Niemann-Pick disease type C.
    Canafoglia L, Bugiani M, Uziel G, Dalla Bernardina B, Ciano C, Scaioli V, Avanzini G, Franceschetti S, Panzica F.
    Mov Disord; 2006 Sep; 21(9):1453-6. PubMed ID: 16755579
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  • 19. A case of Dravet syndrome with cortical myoclonus indicated by jerk-locked back-averaging of electroencephalogram data.
    Kobayashi Y, Hanaoka Y, Akiayma T, Ohmori I, Ouchida M, Yamamoto T, Oka M, Yoshinaga H, Kobayashi K.
    Brain Dev; 2017 Jan; 39(1):75-79. PubMed ID: 27523882
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  • 20. Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations.
    Rubboli G, Franceschetti S, Berkovic SF, Canafoglia L, Gambardella A, Dibbens LM, Riguzzi P, Campieri C, Magaudda A, Tassinari CA, Michelucci R.
    Epilepsia; 2011 Dec; 52(12):2356-63. PubMed ID: 22050460
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