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A 6-Year-Old Girl with Progressive Toe Walking
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Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
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CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
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Spinal Muscular Atrophy A Timely Review
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Neurologic Manifestations of von Hippel-Lindau Disease
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Decoding Cryptogenic Cardioembolism
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Dopamine-Responsive Dystonia
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Learning Disability
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Amyotrophic Lateral Sclerosis
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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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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Spinocerebellar Ataxias and Ataxins
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Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
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New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
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Wilson Disease
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Startle Disease, or Hyperrekplexia:Clonazepam and Assign of Gene (STHE) to Chromosoma 5q by Linkage Analysis
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Detecting Susceptibility to Malignant Hyperthermia
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Cockayne Syndrome: Review of 140 Cases
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Brain Tumors
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Fucosidosis Revisited:A Review of 77 Patients
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Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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