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Cerebroretinal Vasculopathy Mimicking a Brain Tumor:A Case of a Rare Hereditary Syndrome
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Clinicopath Conf
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Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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More Than a Little Unsteady
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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Clinicopathologic Conference,Aceruloplasminemia, Hereditary
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Intracranial Neoplasms and Paraneoplastic Disorders, Meningioma
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CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Genetic Aspects of Alzheimer Disease
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Leukodystrophies: Classification, Diagnosis, and Treatment
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Familiality in Brain Tumors
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Hereditary Infantile Hemiparesis, Retinal Arteriolar Tortuosity, and Leukoencephalopathy
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Primary Brain Tumours in Adults
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Cerebrovascular Manifestations in 321 Cases of Hereditary Hemorrhagic Telangiectasia
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Inclusion Body Myositis and Myopathies
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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
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Turcot's Syndrome:Evidence for Linkage to the Adenomatous Polyposis Coli (APC) Locus
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Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Familial Spinal Neurofibromatosis:Clinical and DNA Linkage Analysis
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Familial Meningioma
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A Familial Syndrome of Dystonia, Blepharospasm, and Pigmentary Retinopathy
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Neurofibromatosis and Other Disorders Among Children with CNS Tumors and Their Families
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Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
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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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