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Showing articles 0 to 10 of 10 Filter Applied: gene mutation (Click to remove) CLOVES Syndrome Neurol 96:e1487-e1488, Collins, M.,et al, 2021 Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man Neurol 88:e26-e29, Qin, C.,et al, 2017 Sturge-Weber Syndrome UptoDate , Nov, Bodensteiner, J.B., 2014 Intracranial Neoplasms and Paraneoplastic Disorders, Oligodendroglioma Adams & Victors Principles of Neurology, Chp 31, pg 654, Ropper, A.H.,et al, 2014 Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014 Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy Neurol 79: e70-e72, Zhong, L.,et al, 2012 Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012 Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) NEJM 360:1656-1665, Case 12-2009, 2009 Metabolic Disease and Stroke: MELAS emedicine.com, Mandava,P.,et al, 2006 The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel NEJM 345:17-24,57, Ducros,A.,et al, 2001 Showing articles 0 to 10 of 10