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Showing articles 0 to 8 of 8 Filter Applied: gene mutation (Click to remove) A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium Neurol 100:631-637, Zeng,T.f.,et al, 2023 Ears of the Lynx Magnetic Resonance Imaging Sign Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020 A Teenager with Persistent Headache Neurol 92:e1526-e1531, Hu, Y.,et al, 2019 Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use Neurol 84:e165-e169, Whitlock, J.B.,et al, 2015 Progressive Gait Deterioration in Adolescents with Dravet Syndrome Arch Neurol 69:873-878, Rodda, J.M.,et al, 2012 Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy Neurol 79: e70-e72, Zhong, L.,et al, 2012 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Clinical Correlations of Mutations in the SCN1A Gene: From Febrile Seizures to Severe Myoclonic Epilepsy in Infancy Pediatr Neurol 30:236-243, Ceulemans,B.P.G.M.,et al, 2004 Showing articles 0 to 8 of 8