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Showing articles 0 to 6 of 6 Filter Applied: myoclonus,epilepsy (Click to remove) 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 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 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 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 Showing articles 0 to 6 of 6