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See Latest ArticlesA Novel MECP2 Mutation in a Boy with Neonatal Encephalopathy and Facial Dysmorphism
The Journal of Pediatrics, 07/01/09
Julich K et al. - Methly-CpG-binding protein 2 mutations cause Rett syndrome in females. Here authros report on a male infant with neonatal encephalopathy, myoclonic jerks, and irregular breathing patterns caused by a novel frameshift mutation in the MECP2 gene. In addition he has facial dysmorphisms previously not described in these patients.
Today in Basic Science/Genetics...keeping you current
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25-Hydroxyvitamin D levels and cognitive performance and decline in elderly men
Neurology, 11/27/09
GAB2 is not associated with late-onset Alzheimers disease in Chinese Han
Neurological Sciences, 11/27/09
Association of Fibrinogen with Parkinson Disease in Elderly Japanese-American Men: A Prospective Study
Neuroepidemiology , 11/27/09
Today in Pediatric Neurology...keeping you current
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Influence of Malnutrition on the Course of Childhood Bacterial Meningitis
The Pediatric Infectious Disease Journal, 11/25/09
Is insufficient quantity and quality of sleep a risk factor for neck, shoulder and low back pain? A longitudinal study among adolescents
European Spine Journal, 11/25/09
Childhood Absence Epilepsy in Patients With Benign Focal Epileptiform Discharges
Pediatric Neurology , 11/24/09
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