Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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RNF213 Polymorphisms in Intracranial Artery Dissection
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Decoding Cryptogenic Cardioembolism
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Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
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Metabolic Disease and Stroke: MELAS
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL
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Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
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CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings
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Clinical Spectrum of CADASIL:A Study of 7 Families
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Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
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Cerebrovascular Disease in Ehlers-Danlos Syndrome Type IV
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Familial Association of Giant Cell Arteritis
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Pseudoxanthoma Elasticum:A Review of Neurological Complications
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Multivessel Cerebral Occlusion in Noonan Syndrome
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Melas Syndrome
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Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
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Neonatal Seizures
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The Phenotypic Continuum of ATP1A3-Related Disorders
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A Middle-aged Woman with Severe Scoliosis and Encephalopathy
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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
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Acute Cortical Lesions in MELAS Syndrome: Anatomic Distribution, Symmetry, and Evolution
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Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
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Neuroimaging Changes in Menkes Disease, Part 1
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A Neonate with Micrognathia and Hypotonia
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The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
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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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Characyeristic features and progression of abnormalities on MRI for CARASIL
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Molybdenum Cofactor Deficiency
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Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
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CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Genomewide Association Studies of Stroke
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A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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Aicardi-Gouti�res Syndrome
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Two Sets of Identical Twins with Cervical Artery Dissection Concordant for Temporal Artery Pathology
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