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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Two Sets of Identical Twins with Cervical Artery Dissection Concordant for Temporal Artery Pathology
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Clinicopathological Conference
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Degenerative Diseases of the Nervous System, Alzheimer Disease
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Clinical Manifestations and Diagnosis of Bicuspid Aortic Valve in Adults
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Heritability of Carotid Artery Atherosclerotic Lesions
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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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Cerebrovascular Disease in Ehlers-Danlos Syndrome Type IV
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Pseudoxanthoma Elasticum:A Review of Neurological Complications
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A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
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Pediatric Leigh Syndrome
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Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
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Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
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Clinical and Neuroimaging Features in Gorlin-Goltz Syndrome
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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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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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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
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Sturge-Weber Syndrome
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Sturge-Weber Syndrome
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Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
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Aicardi-Gouti�res Syndrome
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Autosomal Dominant Moyamoya Disease Maps to Chromosome 17q25.3
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Update on Blepharospasm: Report from the BEBRF International Workshop
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MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
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Parkinsons Disease and Genetics
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The Genetic Causes of Basal Ganglia Calcification, Dementia, and Bone Cysts
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Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q
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Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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Familial Infantile Bilateral Striatal Necrosis
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Clinical Profile of Stroke in 900 Patients with Hypertrophic Cardiomyopathy
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Complete Genomic Screen in Parkinson Disease
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Association Between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
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Hereditary Form of Parkinsonism-Dementia
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CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings
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