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A 14-Year-Old Girl with Headache, Seizures, and Confusion
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
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Hereditary Hemorrhagic Telangiectasia
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
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A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
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Vascular Malformations of the Central Nervous System
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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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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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Amyotrophic Lateral Sclerosis
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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High Prevalence of Spinal Cord Cavernous Malformations in the Familial Cerebral Cavernous Malformations
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Recurrent Cerebral Ischemia During Pregnancies
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A Teenager with Persistent Headache
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A 42-year-old man with unilateral leg weakness
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Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
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Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
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Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
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Neuromyelitis Optica Spectrum Disorders
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Red Papules on the Tongue of a Patient with Hemiparesis
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Vertebral Artery Dissection in Patients with Autosomal Dominant Polycystic Kidney Disease
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Cerebral Amyloid Angiopathy
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CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
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The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
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An unusual cause of stroke and hypoxia
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Optimal Screening Strategy for Familial Intracranial Aneurysms: A Cost-Effectiveness Analysis
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Familial Neuromyelitis Optica
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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Pediatric Moyamoya Disease: An Analysis of 410 Consecutive Cases
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Conventional MRI and NOTCH3 Gene Screening in Sporadic CADASIL
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Genomewide Association Studies of Stroke
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Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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Aicardi-Gouti�res Syndrome
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Genetics of Familial Amyotrophic Lateral Sclerosis
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