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Novel Mutation of Early, Perinatal-Onset, Myopathic-Type Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency
Pediatric Neurology , 08/06/09
Korematsu S et al. – A male neonate demonstrated fetal distress, neonatal asphyxia, and transient hyper–creatine kinase–emia (8400IU/L), followed by repeated episodes of rhabdomyolysis 1–2 times/year during infancy and early childhood.
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Head Motions While Riding Roller Coasters: Implications for Brain Injury
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Today in Pediatric Neurology...keeping you current
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