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Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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A Child with Delayed Motor Milestones and Ptosis
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
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Extending the KCNQ2 encephalopathy Spectrum
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Pediatric Moyamoya Disease: An Analysis of 410 Consecutive Cases
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Update on Blepharospasm: Report from the BEBRF International Workshop
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Hereditary Infantile Hemiparesis, Retinal Arteriolar Tortuosity, and Leukoencephalopathy
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Familial Infantile Bilateral Striatal Necrosis
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A Locus for Febrile Seizures (FEB3) Maps to Chromosome 2q23-24
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Predictors of Recurrent Febrile Seizures
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Tourette's Syndrome:A Model Neuropsychiatric Disorder
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Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
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Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
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The Relationship of Essential Tremor to Other Movement Disorders:Report on 678 Patients
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Tourette's Syndrome in Monozygotic Twins:Relationship of Tic Severity to Neuropsychological Function
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Seizure Characteristics in Chromosome 20 Benign Familial Neonatal Convulsions
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Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
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A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
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A Clinical Study of Noonan Syndrome
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Essential Tremor:Clinical Correlates in 350 Patients
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Benign Familial Neonatal Convulsions:Evidence for Clinical and Genetic Heterogeneity
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