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Pediatric Research
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March 30, 2012
Pulmonary vascular resistance in repaired congenital diaphragmatic hernia vs. age-matched controls
Matthew E Zussman, Michelle Bagby, D Woodrow Benson, et al.
Journal of the American College of Cardiology
|
July 6, 2004
Bicuspid aortic valve is heritable
Linda Cripe, Gregor Andelfinger, Lisa J Martin, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
November 1, 1978
An ultrastructural study of the development of nephritis in mice treated with interferon in the neonatal period
L Morel-Maroger, J C Sloper, J Vinter, et al.
International Journal of Cancer
|
May 15, 1994
Interaction of IFN alpha/beta with host cells essential to the early inhibition of Friend erythroleukemia visceral metastases in mice
I Gresser, T Kaido, C Maury, et al.
Gene Therapy
|
February 19, 1999
Prevention of collagen-induced arthritis by gene delivery of soluble p75 tumour necrosis factor receptor
R A Mageed, G Adams, D Woodrow, et al.
Human Molecular Genetics
|
March 3, 2009
Analysis of Ellis van Creveld syndrome gene products: implications for cardiovascular development and disease
Kristen Lipscomb Sund, Stephanie Roelker, Vijaya Ramachandran, et al.
Journal of the American College of Cardiology
|
October 4, 2005
ACCF/AHA/AAP recommendations for training in pediatric cardiology. Task force 7: training guidelines for research in pediatric cardiology
D Woodrow Benson, H Scott Baldwin, Larry T Mahoney, et al.
Heartrhythm Case Reports
|
September 23, 2021
Classic and atypical Wenckebach periodicity in a late gestation fetus with maternal anti-Ro/SSA antibodies
Melanie R F Gropler, Johannes von Alvensleben, D Woodrow Benson, et al.
Biological Research for Nursing
|
October 9, 2003
A candidate locus approach identifies a long QT syndrome gene mutation
Theresa A Beery, Macaira Dyment, Kerry Shooner, et al.
Heart Rhythm
|
February 29, 2012
Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutation
Ji Kwon Park, Lisa J Martin, Xue Zhang, et al.
Page
of 18
Search research articles
Search
Showing results (51-60 of 177) with videos related to
Sort By:
Page
of 18
Pediatric Research
|
March 30, 2012
Pulmonary vascular resistance in repaired congenital diaphragmatic hernia vs. age-matched controls
Matthew E Zussman, Michelle Bagby, D Woodrow Benson, et al.
Journal of the American College of Cardiology
|
July 6, 2004
Bicuspid aortic valve is heritable
Linda Cripe, Gregor Andelfinger, Lisa J Martin, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
November 1, 1978
An ultrastructural study of the development of nephritis in mice treated with interferon in the neonatal period
L Morel-Maroger, J C Sloper, J Vinter, et al.
International Journal of Cancer
|
May 15, 1994
Interaction of IFN alpha/beta with host cells essential to the early inhibition of Friend erythroleukemia visceral metastases in mice
I Gresser, T Kaido, C Maury, et al.
Gene Therapy
|
February 19, 1999
Prevention of collagen-induced arthritis by gene delivery of soluble p75 tumour necrosis factor receptor
R A Mageed, G Adams, D Woodrow, et al.
Human Molecular Genetics
|
March 3, 2009
Analysis of Ellis van Creveld syndrome gene products: implications for cardiovascular development and disease
Kristen Lipscomb Sund, Stephanie Roelker, Vijaya Ramachandran, et al.
Journal of the American College of Cardiology
|
October 4, 2005
ACCF/AHA/AAP recommendations for training in pediatric cardiology. Task force 7: training guidelines for research in pediatric cardiology
D Woodrow Benson, H Scott Baldwin, Larry T Mahoney, et al.
Heartrhythm Case Reports
|
September 23, 2021
Classic and atypical Wenckebach periodicity in a late gestation fetus with maternal anti-Ro/SSA antibodies
Melanie R F Gropler, Johannes von Alvensleben, D Woodrow Benson, et al.
Biological Research for Nursing
|
October 9, 2003
A candidate locus approach identifies a long QT syndrome gene mutation
Theresa A Beery, Macaira Dyment, Kerry Shooner, et al.
Heart Rhythm
|
February 29, 2012
Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutation
Ji Kwon Park, Lisa J Martin, Xue Zhang, et al.
Page
of 18