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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Hereditary Hemorrhagic Telangiectasia, Clinical Presentations, and Management
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Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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A 14-Year-Old Girl with Headache, Seizures, and Confusion
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Ehlers-Danlos Syndromes
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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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Red Papules on the Tongue of a Patient with Hemiparesis
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An unusual cause of stroke and hypoxia
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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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Aicardi-Gouti�res Syndrome
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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)
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Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Angiographic and Clinical Characteristics of Patients with Cerebral Arteriovenous Malformations Associated with Hereditary Hemorrhagic Telangiectasia
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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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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Hereditary Leukoencephalopathy and Palmoplantar Keratoderma:A New Disorder with Increased Skin Collagen Content
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Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
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Hereditary Hemorrhagic Telangiectasia
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Cerebrovascular Complications in Ehlers-Danlos Syndrome Type IV
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Familial Sneddon's Syndrome:Clinical, Hematologic, and Radiographic Findings in Two Brothers
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Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
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A Clinical Study of Noonan Syndrome
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Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
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Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
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Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
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An Autosomal Dominant Syndrome of Hemiplegic Migraine, Nystagmus, & Tremor
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