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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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Detection of Cytomegalovirus DNA in Dried Blood Spots of Minnesota Infants Who Do Not Pass Newborn Hearing Screening
The Pediatric Infectious Disease Journal, 10/14/09
Genetics of food allergy
Current Opinion in Pediatrics, 10/23/09
Genetic forms of hypopituitarism and their manifestation in the neonatal period
Early Human Development, 10/30/09
Today in Pediatric Neurology...keeping you current
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Cardiometabolic Risk of Second-Generation Antipsychotic Medications During First-Time Use in Children and Adolescents
JAMA, 10/28/09
Risk factors for valproic acid resistance in childhood absence epilepsy
Seizure - European Journal of Epilepsy, 10/21/09
Intellectual Deficits in Children with ADHD Beyond Central Executive and Non-Executive Functions
Archives of Clinical Neurospsychology, 10/16/09
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