Spinal Muscular Atrophy
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Clinicopathologic Conference, Homocystinuria due to genetic mutations of the gene encoding cystathionine B-synthase (CBS)
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Clinical and Neuroimaging Features in Gorlin-Goltz Syndrome
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Neurodevelopment and Cognition in Children After Enterovirus 71 Infection
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Neurologic and Developmental Disability After Extremely Preterm Birth
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
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Neurodevelopmental Outcome of Infants with Hypoplastic Left Heart Syndrome
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Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
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Significance of Seizures Associated with Extracorporeal Membrane Oxygenation
J Pediatr 119:789-792, Campbell,L.R.,et al, 1991
Fucosidosis Revisited:A Review of 77 Patients
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Neurological Deterioration in Young Adults with Phenylketonuria
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Brain Damage by Neonatal Hypoglycaemia
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