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Neurofibromatosis Type 2
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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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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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Central Nervous System Haemangioblastoma:A Clinical & Genetic Study of 52 Cases
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Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
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A Family Affected with Intestinal Polyposis & Gliomas
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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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Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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Neonatal Seizures
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Hematologic Disorders and Ischemic Stroke
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Occurrence of Both Neurofibromatosis 1 and 2 in the Same Individual with a Rapidly Progressive Course
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Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
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Neurologic Aspects of Hereditary Hemorrhagic Telangiectasia
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
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Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
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Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
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The Spectrum of Fragile X Disorders
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A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
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Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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