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The Tuberous Sclerosis Complex
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Mendelian Etiologies of Stroke
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Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
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Neurological Management of Von Hippel-Lindau Disease
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
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Recessive Ataxia With Ocular Apraxia
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Cerebroretinal Vasculopathy Mimicking a Brain Tumor:A Case of a Rare Hereditary Syndrome
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Congential Deficienty of Factor VII in Subarachnoid Hemorrhage
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Turcot's Syndrome:Evidence for Linkage to the Adenomatous Polyposis Coli (APC) Locus
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Molecular Genetics in Neurology
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Familial Intracranial Haemorrhage Due to Factor V Deficiency
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New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
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Angelman Syndrome: Clinical Profile
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Central Nervous System Involvement in Von Hippel-Lindau Disease
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Familial Spinal Neurofibromatosis:Clinical and DNA Linkage Analysis
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Fucosidosis Revisited:A Review of 77 Patients
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Neurofibromatosis Type I in Children
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Central Nervous System Haemangioblastoma:A Clinical & Genetic Study of 52 Cases
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Hematologic Disorders and Ischemic Stroke
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Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
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Occurrence of Both Neurofibromatosis 1 and 2 in the Same Individual with a Rapidly Progressive Course
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Radiologic Screening for von Hippel-Lindau Disease:Role of Gd-DTPA Enhanced MR Imaging of the CNS
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Neurofibromatosis 2:Clinical & DNA Linkage Studies of a Large Kindred
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Nevoid Basal Cell Carcinoma Syndrome & Epilepsy
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Von Recklinghausen Neurofibromatosis
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A Family Affected with Intestinal Polyposis & Gliomas
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Studies in Aging of the Brain:IV. Familial Alzheimer Dis. :Relat. to Transmiss. Demetia, Aneuploidy, & Microtubular Defects
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Meningiomas in Five Members of a Family Over Two Generations, in One Member Simultaneously with Acoustic Neurinomas
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Neuroectodermal Tumors in the Cerebellum in Two Sisters
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
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A 6-Year-Old Girl with Progressive Toe Walking
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
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A 22-Year-Old Man with Progressive Bilateral Visual Loss
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