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See Latest ArticlesPTPN11 Mutation Associated with Aortic Dilation and Hypertrophic Cardiomyopathy in a Pediatric Patient with Noonan Syndrome
Pediatric Cardiology, 10/12/09
Jefferies JL et al. – The authors describe an 8–year–old girl who had Noonan syndrome involving a PTPN11 mutation, hypertrophic cardiomyopathy, main pulmonary artery dilation, and aortic root dilation. This is the first case in which all three of these cardiovascular features have been observed in a single patient with Noonan syndrome.
Today in Basic Science/Genetics...keeping you current
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Neonatal seizures and Long QT Syndrome: A cardiocerebral channelopathy
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Today in Pediatric Cardiology...keeping you current
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Oral Ibuprofen and Ductus Arteriosus Closure in Full-Term Neonates: A Prospective Case-Control Study
Pediatric Cardiology, 10/30/09
Population-based analysis of sudden death in children: The Oregon Sudden Unexpected Death Study
Heart Rhythm, 11/04/09
Electrocardiographic Screening in Children With Attention-Deficit Hyperactivity Disorder
The American Journal of Cardiology, 10/22/09
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