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Recurrent Cerebral Ischemia During Pregnancies
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Muscular Dystrophies
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Neurological Management of Von Hippel-Lindau Disease
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Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
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An unusual cause of stroke and hypoxia
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
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Diagnosis and New Treatments in Muscular Dystrophies
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Tuberous Sclerosis
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Familiality in Brain Tumors
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Von Recklinghausen's Neurofibromatosis: Neurofibromatosis Type 1
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Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope
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Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene
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Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Turcot's Syndrome:Evidence for Linkage to the Adenomatous Polyposis Coli (APC) Locus
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Leber's Hereditary Optic Neuropathy as a Cause of Severe Visual Loss in Childhood
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Brain Tumors
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Neurofibromatosis Type I in Children
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Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
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Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
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Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
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Neurofibromatosis 2:Clinical & DNA Linkage Studies of a Large Kindred
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Anderson-Fabray Disease, A Commonly Missed Diagnosis
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