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See Latest ArticlesRolandic Mitochondrial Encephalomyelopathy and MT-ND3 Mutations
Pediatric Neurology , 06/26/09
Werner KGE et al. - Bilateral rolandic lesions and epilepsia partialis continua accompanied by suspicion of mitochondrial disease are indications to search for an underlying mutation in the MT-ND3 gene.
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Examining the Cardiac NK-2 Genes in Early Heart Development
Pediatric Cardiology, 12/20/09
Single Cell Analysis of Mutations in the APC Gene
Fetal Diagnosis and Therapy, 12/19/09
Developmental changes of the contingent negative variation in migraine and healthy children
The Journal of Headache and Pain, 12/18/09
Today in Pediatric Neurology...keeping you current
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An uncommon illness with a rare presentation: neurosurgical management of ADEM with tumefactive demyelination in children
Child's Nervous System, 12/20/09
Stimulation threshold potentials of intraoperative cortical motor mapping using monopolar trains of five in pediatric epilepsy surgery
Child's Nervous System, 12/19/09
Effects of pain management on sleep in preterm infants
European Journal of Pain, 12/18/09
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