Metabolic Disease and Stroke: MELAS
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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Ehlers-Danlos Syndromes
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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Familial Subarachnoid Hemorrhage:Distinctive Features and Patterns of Inheritance
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Hereditary Hemorrhagic Telangiectasia
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Congential Deficienty of Factor VII in Subarachnoid Hemorrhage
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Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
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Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
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Mendelian Etiologies of Stroke
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Clinodactyly as a Key Finding in Distal Spinal Muscular Atrophy
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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Neonatal Seizures
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A Middle-aged Woman with Severe Scoliosis and Encephalopathy
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"Disappearing Infarct" Is Late-Onset MELAS
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Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
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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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Neuroimaging Changes in Menkes Disease, Part 1
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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MRI Findings of Biotin-Responsive Basal Ganglia Disease Before and After Treatment
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Hydrocephalus in Children
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A Young Man with Progressive Vision and Hearing Loss
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Neurological Management of Von Hippel-Lindau Disease
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Sturge-Weber Syndrome
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Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
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Inherited Metabolic Diseases of the Nervous System, Infantile Gaucher Disease
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Inherited Metabolic Diseases of the Nervous System, Neuroaxonal Dystrophy
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Sturge-Weber Syndrome
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Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
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The Autosomal Recessive Cerebellar Ataxias
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CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
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Restricted Diffusion in Vanishing White Matter
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