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Pediatric Cardiology|October 2, 2009
PTPN11 mutation associated with aortic dilation and hypertrophic cardiomyopathy in a pediatric patient with Noonan syndromeJohn L Jefferies, John W Belmont, Ricardo Pignatelli, et al.
The American Journal of Cardiology|August 15, 1997
A genetic etiology for interruption of the aortic arch type BM B Lewin, E A Lindsay, V Jurecic, et al.
Pediatric Neuroscience|January 1, 1985
Benign extra-axial collections of infancyP L Carolan, R L McLaurin, R B Towbin, et al.
Circulation|August 23, 2000
Sudden death and cardiovascular collapse in children with restrictive cardiomyopathyS M Rivenes, D L Kearney, E O Smith, et al.
The Journal of Thoracic and Cardiovascular Surgery|October 10, 1998
Adenovirus infection in the lung results in graft failure after lung transplantationN D Bridges, T L Spray, M H Collins, et al.
American Journal of Medical Genetics|January 23, 1999
Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIBR Kosaki, M Gebbia, K Kosaki, et al.
Texas Heart Institute Journal|January 1, 1997
The rare association of tetralogy of Fallot with hypertrophic cardiomyopathy. Report of 2 neonatal patientsM B Lewin, J A Towbin, M K Thapar, et al.
Journal of Cardiology Cases|December 15, 2018
Left ventricular noncompaction cardiomyopathy in Duchenne muscular dystrophy carriersJohn J Parent, Ryan A Moore, Michael D Taylor, et al.
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