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Showing articles 0 to 6 of 6 Filter Applied: familial (Click to remove) Complex Ataxia Neurol 95:136-141, Abkur, T.,et al, 2020 Essential Tremor NEJM 378:1802-1810, Haubenberger, D.,et al, 2018 Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis NEJM 364:1062-1074, Case 8-2011, 2011 Benign Tremulous Parkinsonism Arch Neurol 63:354-357,321, Josephs,K.A.,et al, 2006 Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Showing articles 0 to 6 of 6