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Showing articles 0 to 14 of 14 Filter Applied: familial (Click to remove) Thyrotoxic Periodic Paralysis UptoDate Jan, Gutmann, L. & Conwit, R., 2022 Personality Changes, Executive Dysfunction, and Motor and Memory Impairment JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017 A Child with Delayed Motor Milestones and Ptosis Neurol 88:e158-e163, Ghosh, P.S., 2017 Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes) NEJM 376:1668-1678, CASE 13-2017, 2017 A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes Ann Neurol 77:1-7, Scripko, P.,et al, 2015 Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation JNNP 69: 5-12, Gray,R.G.F. et al, 2000 Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998 NEJM 339:1914-1923, , 1998 Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995 Myasthenic Symptoms in Patients with Mitochondrial Myopathies Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995 Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency Neurol 44:461-466, Wilkinson,D.A.,et al, 1994 Monomelic Amyotrophy Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994 Hereditary Long Q-T Syndrome Presenting as Epilepsy:Electroencephalography Laboratory Diagnosis Ann Neurol 25:514-516, Gospe,S.M.&Choy,M., 1989 Paroxysmal Cerebellar Ataxia Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989 Phosphorylase Deficiency In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986 Showing articles 0 to 14 of 14