Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Neuromyelitis Optica Spectrum Disorders
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Update on Blepharospasm: Report from the BEBRF International Workshop
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Paroxysmal Extreme Pain Disorder (Previously Familial Rectal Pain Syndrome)
Neurol 69:586-595, Fertleman,C.R.,et al, 2007
Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006
Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Recurrent Orbital Myositis,Report of a Familial Incidence
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
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Anticonvulsant Hypersensitivity Syndrome
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Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991
Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989
Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
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An Autosomal Dominant Syndrome of Hemiplegic Migraine, Nystagmus, & Tremor
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