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59. Abstract 12940: Shared Senescence Pathophysiology in Preeclampsia and Peripartum Cardiomyopathy

60. Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies

62. Proinflammatory TH17 cytokine activation, disease severity and outcomes in peripartum cardiomyopathy

64. Genetic Variants Are Not Associated with Outcome in Patients with Coronary Artery Disease and Left Ventricular Dysfunction: Results of the Genetic Substudy of the Surgical Treatment for Ischemic Heart Failure (STICH) Trials

66. Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease

67. Heart Failure Association of the ESC, Heart Failure Society of America and Japanese Heart Failure Society Position statement on endomyocardial biopsy

68. Genetic and Phenotypic Landscape of Peripartum Cardiomyopathy

76. Contributors

78. Association between the severity of angiographic coronary artery disease and paraoxonase gene polymorphisms in the National Heart, Lung, and Blood Institute-sponsored Women's Ischemia Syndrome Evaluation (WISE) study

82. Heart Transplantation

84. Peripartum Cardiomyopathy

85. Breastfeeding, Cellular Immune Activation, and Myocardial Recovery in Peripartum Cardiomyopathy

86. Reply

94. Myocarditis

96. Serum protein profiles predict coronary artery disease in symptomatic patients referred for coronary angiography

97. Electromagnetic Interference from Left Ventricular Assist Device (LVAD) Inhibiting the Pacing Function of an Implantable Cardioverter-Defibrillator (ICD) Device

100. Elevated Sera sST2 Is Associated With Heart Failure in Men ≤50 Years Old With Myocarditis

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