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Neuroimaging Features of Biotinidase Deficiency
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Recurrent Cerebral Ischemia During Pregnancies
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Fibromuscular Dysplasia and Its Neurologic Manifestations
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Amyotrophic Lateral Sclerosis
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MRI Findings of Biotin-Responsive Basal Ganglia Disease Before and After Treatment
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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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Degenerative Diseases of the Nervous System, Friedreich Ataxia
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Parkin Disease
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The Autosomal Recessive Cerebellar Ataxias
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Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
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The Ever-Expanding Spectrum of Congenital Muscular Dystrophies
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Clinical Reasoning: A Case of Treatable Spastic Paraparesis
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Dopa-Responsive Dystonia Revisited
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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A Multidisciplinary Study of Patients with Early-Onset PD with and Without Parkin Mutations
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Diagnosis and New Treatments in Muscular Dystrophies
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Neurofibromatosis
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Tuberous Sclerosis
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Parkinsons Disease and Genetics
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The Tuberous Sclerosis Complex
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Parkinson's Disease
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Association of Multidrug Resistance in Epilepsy with a Polymorphism in the Drug-Transporter Gene ABCB1
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Amyotrophic Lateral Sclerosis
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Complete Genomic Screen in Parkinson Disease
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Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene
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Association Between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
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N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
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Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects
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The Muscular Dystrophies
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The Diagnostic Evaluation & Multidisciplinary Management of Neurofibromatosis 1 and Neurofibromatosis 2
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X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Spinocerebellar Ataxias and Ataxins
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Hereditary Hemorrhagic Telangiectasia
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Myoblast Transfer in Duchenne Muscular Dystrophy
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