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Showing articles 0 to 8 of 8 Filter Applied: myoclonus,epilepsy (Click to remove) Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis NEJM 364:1062-1074, Case 8-2011, 2011 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 CSF Antigliadin Antibodies and the Ramsay Hunt Syndrome Neurol 49:1131-1133, Chinnery,P.F.,et al, 1997 Progr Myoclonus Epilepsy of Unverricht-Lundborg Type:Clin & Molecular Genetic Study from US 4 Affected Sibs Neurol 43:2284-2286, Lehesjoki,A.E.,et al, 1993 Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family Neurol 38:1065-1070, Takahashi,H.,et al, 1988 Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features Ann Neurol 3:419, Dorfman,L.J.,et al, 1978 Chronic Progressive Panencephalitis due to Rubella Virus Simulating Subacute Sclerosing Panencephalitis NEJM 292:994-998,1023, Weil, M.L.,et al, 1975 Showing articles 0 to 8 of 8