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The Occurence of Guillain-Barre Syndrome Within Families
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Cardiac Dysfunction in Neuromuscular Diseases
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Cerebromeningeal Haemophagocytic Lymphohistiocytosis
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Polyneroupathies of Undetermined Cause
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A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
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Hereditary Hemorrhagic Telangiectasia, Clinical Presentations, and Management
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Recurrent Cerebral Ischemia During Pregnancies
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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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Clinical Reasoning: A Teenager with Left Arm Weakness
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Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
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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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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Degenerative Diseases of the Nervous System, Parkinson Disease
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Cerebral Amyloid Angiopathy
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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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Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
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Restless Legs Syndrome: Is Treatable But Under-Recognised
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Migraine and Cerebral White Matter Lesions
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Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Bicuspid Aortic Valve - A Silent Danger: Analysis of 50 Cases of Infective Endocarditis
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Hereditary Spastic Paraplegia:Advances in Genetic Research
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Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
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DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction:POLIP Syndrome
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Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
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Acid Maltase Deficiency
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More Than a Little Unsteady
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Amyotrophic Lateral Sclerosis
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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A 53-year-old Woman with Lower Extremity Paresthesias
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Complex Ataxia
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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