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Showing articles 0 to 12 of 12 Filter Applied: genetic neurologic disorders (Click to remove) The Autosomal Recessive Cerebellar Ataxias NEJM 366:636-646, Anheim,M.,et al, 2012 CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis Neurol 78:1150-1156, Deiva,K.,et al, 2012 A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review The Neurologist 8:302-312, Thambisetty,M.,et al, 2002 Leigh Disease (Subacute Necrotizing Encephalomyelopathy) :CT & MR in Five Cases J Comput Assist Tomogr 12:40-44, Geyer,C.A.,et al, 1988 Cerebral Cavernous Malformations:Incidence and Familial Occurrence NEJM 319:343-347, Rigamonti,D.,et al, 1988 A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever Neurol 102:e209358, Barbosa,A.R.,et al, 2024 A 22-Year-Old Man with Progressive Bilateral Visual Loss Neurol 94:625-630, Yang, S.L.,et al, 2020 Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2 NEJM 370:911-920, Zhou, Q.,et al, 2014 Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis NEJM 364:1062-1074, Case 8-2011, 2011 Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up AJNR 30:1971-1976, Uggetti,C.,et al, 2009 Aicardi-Gouti�res Syndrome Br Med Bull 89:183-201, Orcesi, S.,et al, 2009 Periodic Meningitis & Familial Mediterranean Fever Arch Int Med 142:378-379, Vilaseca,J.,et al, 1982 Showing articles 0 to 12 of 12