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Congenital Muscular Dystrophy
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A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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Spinal Muscular Atrophy
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Duchenne Muscular Dystrophy
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Case 35-2006: A Newborn Boy with Hypotonia
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Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002
Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
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Recognising & Preventing Duchenne Muscular Dystrophy
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Diagnostic Delay in Duchenne's Muscular Dystrophy
JAMA 247:478-480, Crisp,D.E.,et al, 1982
The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
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Glycogen-Storage Disease Type II
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Neurologic Status of HIV-1 Infected Infants and Their Controls:A Prospective Study from Birth to 2 Yrs
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Effects of HIV on Cognitive & Motor Devel in Children Born to HIV-Seropositive Women with no Reported Drug Use:Birth-24 mo
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Cognitive and Motor Development in Infants at Risk for Human Immunodeficiency Virus
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Defective Glucose Transport Across the Blood-Brain Barrier as Cause of Hypoglycorrhachia, Seizures, and Devel Delay
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Joubert Syndrome:A Clinico-Radiological Study
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Congenital AIDS:Review of Neurological Problems
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Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
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Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
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Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy
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Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
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