Spinal Muscular Atrophy
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Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
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Lumbosacral Radiculomyelitis Assoc with Pandemic Acute Hemorrhagic Conjunctivitis
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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Clinicopathologic Conference, Infant Botulism, Case 3-2024
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A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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A Young Woman with Rapidly Progressive Weakness and Paresthesia
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The Phenotypic Continuum of ATP1A3-Related Disorders
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A Teenager with Shortness of Breath and Difficulty Walking
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Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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Degenerative Diseases of the Nervous System, Werdnig-Hoffman Disease, Spinal Muscular Atrophy
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The Autosomal Recessive Cerebellar Ataxias
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
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The Floppy Infant: Evaluation of Hypotonia
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Aicardi-Gouti�res Syndrome
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A Floppy Child with Failure to Thrive
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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Transsection of the Spinal Cord Associated with Breech Delivery
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
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Central Core Disease, Clinical Features in 13 Patients
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Ultrastructural, Neurological, & Glycosaminoglycan Abnormalities in Lowe's Syndrome
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Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
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Neuro CPC of MGH
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