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Actionable Diagnosis of Neuroleptospirosis by Next-Generation Sequencing
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The Autosomal Recessive Cerebellar Ataxias
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The Tuberous Sclerosis Complex
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Pediatric Leigh Syndrome
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A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis
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Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
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Spinal Muscular Atrophy A Timely Review
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Diagnosis and New Treatment in Muscle Channelopathies
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A 23-Year-Old Man With Seizures and Visual Deficit
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Whipples Disease
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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Fragile X Premutation With Atypical Symptoms at Onset
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Unusual Variants of Alexander's Disease
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Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
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Aromatic L-Amino Acid Decarboxylase Deficiency
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Practice Parameter: Evaluation of the Child with Global Developmental Delay
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Gliomatosis Cerebri: Molecular Pathology and Clinical Course
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Trinucleotide Repeat Expansion in Neurological Disease
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Leber's Hereditary Optic Neuropathy, New Genetic Considerations
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Gene Therapy for Neurologic Disease
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