From Molecule to Men
Molecular Basis of Congenital Cardiovascular Disorders
Published on 1. January 2000
Book
Hardback
X, 246 pages
978-3-7985-1168-2 (ISBN)
Description
From molecule to man: Medical research has indeed taken this direction, and major improvements of our understanding of the pathophysiology and epidemiology of disease have been achieved. The molecular basis of the congenital cardiovascular disorders has been extended from relatively few congenital malformations into everyday illnesses such as diabetes mellitus, hyperlipoproteinaemea, and arterial hypertension. The monogenic and, more difficult, polygenic basis for a vast majority of cardiovascular disorders are being defined more precisely from year to year. This book gives an overview of what has been achieved so far and defines the current position.
More details
Edition
2000 ed.
Language
English
Place of publication
Heidelberg
Germany
Target group
Professional and scholarly
Research
Illustrations
X, 246 p.
Dimensions
Height: 240 mm
Width: 170 mm
Thickness: 19 mm
Weight
592 gr
ISBN-13
978-3-7985-1168-2 (9783798511682)
DOI
10.1007/978-3-642-57724-6
Schweitzer Classification
Other editions
Additional editions
M. Zehender | G. Breithardt | H. Just
From Molecule to Men
Molecular Basis of Congenital Cardiovascular Disorders
E-Book
12/2012
Steinkopff
€96.29
Available for download
M. Zehender | G. Breithardt | H. Just
From Molecule to Men
Molecular Basis of Congenital Cardiovascular Disorders
Book
10/2012
Steinkopff
€106.99
Shipment within 7-9 days
Content
Molecular Basis of Congenital Cardiovascular Disorders.- Genetics 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?.- Angiogenesis and gene therapy.- Genetic engineering for human bypass vein grafts.- Molecular cardiology and physician.