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The Floppy Infant: Evaluation of Hypotonia
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Human Botulism Immune Globulin for the Treatment of Infant Botulism
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Case 35-2006: A Newborn Boy with Hypotonia
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Prader-Willi and Angelman Syndromes
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Leukotriene C4-synthesis Deficiency:A New Inborn Error of Metabolism Linked to a Fatal Developmental Syndrome
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An Infant with Encephalitis
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Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Causal Heterogeneity in Isolated Lissencephaly
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Congenital Inflammatory Myopathy
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Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl
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Congenital Muscular Dystrophy
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Rett Syndrome:Natural History and Management
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Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
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Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
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Hyperphenylalaninemia Due To A Deficiency of Biopterin
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Guillain-Barre Syndrome with Hydrocephalus in Early Infancy
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