Steinkopff Imprint: Steinkopff 2000
Inhaltsangabe:
“… Molecular Basis of Congenital Cardiovascular DisordersGenetics of dilated cardiomyopathy -- Registry of families with inherited dilated cardiomyopathy for molecular analyses -- Distinct phenotype patterns of Ca2+ handling proteins in end-stage failing human hearts -- Apoptosis in the overloaded myocardium: potential stimuli and modifying signals -- Analysis of inherited causes of hypertrophic cardiomyopathy as part of clinical practice -- Molecular genetics of arrhythmogenic right ventricular cardiomyopathy -- Cardiomyopathy: Genetics in muscular dystrophies -- Molecular impact of ion channel mutations for the pathogenesis of long-QT (LQT) syndromes -- Acquired abnormal QT prolongation and torsade de pointes - clinical significance of genetic information from congenital long QT syndrome -- Molecular genetic approaches to human hypertension -- Renin-angiotensin system and coronary artery disease - Interaction of angiotensin II with pro-inflammatory cytokines in human stable and unstable coronary plaques -- Genetics of Lipoprotein(a) -- The molecular mechanisms of inherited hypercholesterolemia -- Insulin resistance: A pathogenic link between cardiovascular risk factors and atherosclerosis -- Genetic control of hemostatic factors in relation to atherosclerosis -- Increased platelet aggregability associated with platelet GPIIIa PIA2 polymorphism: the
Framingham Offspring Study -- Genetic aspects of chronobiologic rhythms in cardiovascular disease -- Is capillary sprouting enough? …”
Signatur:
Wird geladen …
Standort:
Wird geladen …
Book/Monograph
Online Resource