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Imaging Patterns Characterizing Mitochondrial Leukodystrophies
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Neurological Manifestations of Fabry Disease in Female Carriers
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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Neonatal Seizures
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
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Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
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Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
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The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
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Neurological Management of Von Hippel-Lindau Disease
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Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
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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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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
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The Tuberous Sclerosis Complex
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Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Familial Form of Intracranial Cavernous Angioma:MR Imaging Findings in 51 Families
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Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
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Hereditary Cerebral Cavernous Angiomas:Clinical and Genetic Features in 57 French Families
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Linkiage of Locus for Cerebral Cavernous Hemagiomas to Chromosome 7q in 4 Families of Mexican-American Descent
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Stroke in Williams Syndrome
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Cerebrovascular Complications of Fabry's Disease
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Familial Subarachnoid Hemorrhage:Distinctive Features and Patterns of Inheritance
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Hereditary Hemorrhagic Telangiectasia
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Screening Family Members of Patients with Hereditary Hemorrhagic Telangiectasia
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Seizure Characteristics in Chromosome 20 Benign Familial Neonatal Convulsions
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Molecular Genetics in Neurology
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Progressive Vison Loss, A Rare Manifestation of Familial Cavernous Angiomas
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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Benign Familial Neonatal Convulsions:Evidence for Clinical and Genetic Heterogeneity
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Intracranial Hemorrhage in Patients with Polycystic Kidney Disease
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Magnetic Resonance Imaging in a Family with Hereditary Cerebral Arteriovenous Malformations
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Neurofibromatosis and Other Disorders Among Children with CNS Tumors and Their Families
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Cerebral Cavernous Malformations:Incidence and Familial Occurrence
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Livedo Reticularis, Porcelain-White Scars, and Cerebral Thromboses
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Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
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Familial Cavernous Malformations of the Central Nervous System & Retina
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Mendelian Etiologies of Stroke
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