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Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding

Human mutation, 2006-06, Vol.27 (6), p.599-600

2006

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Postextrasystolic regulation patterns of blood pressure and heart rate in patients with idiopathic dilated cardiomyopathy

The Journal of physiology, 2002-01, Vol.538 (1), p.271-278

2002

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Measurement of left ventricular dimensions and function in patients with dilated cardiomyopathy

Journal of magnetic resonance imaging, 2001-03, Vol.13 (3), p.367-371

2001

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Unequal allelic expression of wild-type and mutated β-myosin in familial hypertrophic cardiomyopathy

Basic research in cardiology, 2011-11, Vol.106 (6), p.1041-1055

2011

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DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy

Human mutation, 2008-06, Vol.29 (6), p.879-885

2008

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Dysfunction of dysferlin-deficient hearts

Journal of molecular medicine (Berlin, Germany), 2007-11, Vol.85 (11), p.1203-1214

2007

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Composite polymorphisms in the ryanodine receptor 2 gene associated with arrhythmogenic right ventricular cardiomyopathy

Cardiovascular research, 2006-08, Vol.71 (3), p.496-505

2006

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Increased Susceptibility to Complement Attack due to Down-Regulation of Decay-Accelerating Factor/CD55 in Dysferlin-Deficient Muscular Dystrophy

The Journal of immunology (1950), 2005-11, Vol.175 (9), p.6219-6225

2005

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Bisoprolol vs. carvedilol in elderly patients with heart failure: rationale and design of the CIBIS-ELD trial

Clinical research in cardiology, 2008-09, Vol.97 (9), p.578-586

2008

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Die arrhythmogene rechtsventrikuläre Kardiomyopathie

Herz, 2005-09, Vol.30 (6), p.565-570

2005

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Advanced analysis of spontaneous baroreflex sensitivity, blood pressure and heart rate variability in patients with dilated cardiomyopathy

Clinical science (1979), 2002-04, Vol.102 (4), p.465

2002

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Hypertrophic cardiomyopathy-related beta-myosin mutations cause highly variable calcium sensitivity with functional imbalances among individual muscle cells

American journal of physiology. Heart and circulatory physiology, 2005-03, Vol.288 (3), p.H1242-H1251

2005

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Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: Demand for strategies in the management of presymptomatic lamin A/C mutant carriers

European journal of heart failure, 2006-08, Vol.8 (5), p.484-493

2006

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A rapid protocol for cardiac troponin T gene mutation detection in familial hypertrophic cardiomyopathy

Human mutation, 1998, Vol.11 (2), p.179-182

1998

Volltextzugriff (PDF)

Cardiac energetics correlates to myocardial hypertrophy in Friedreich's ataxia

Annals of neurology, 2003-01, Vol.53 (1), p.121-123

2003

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The G-231A Polymorphism in the Endothelin-A Receptor Gene Is Associated With Lower Aortic Pressure in Patients With Dilated Cardiomyopathy

American journal of hypertension, 2007, Vol.20 (1), p.32-37

2007

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Growth Hormone Treatment in Dilated Cardiomyopathy

Journal of cardiac surgery, 2001-03, Vol.16 (2), p.127-131

2001

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Angiotensin-Converting Enzyme and Heart Chymase gene Polymorphisms in Hypertrophic Cardiomyopathy

The American journal of cardiology, 1996-08, Vol.78 (3), p.362-364

1996

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Uric acid and survival in chronic heart failure: Validation and application in metabolic, functional, and hemodynamic staging

Circulation (New York, N.Y.), 2003-04, Vol.107 (15), p.1991-1997

2003

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Fabry disease: focus on cardiac manifestations and molecular mechanisms

Herz, 2002-11, Vol.27 (7), p.699-702

2002

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Dilated cardiomyopathy: more genes means more phenotypes

European heart journal, 2005-04, Vol.26 (8), p.751-754

2005

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Improved clinical outcome after intracoronary administration of bone-marrow-derived progenitor cells in acute myocardial infarction: final 1 year results of the REPAIR-AMI trial

European heart journal, 2007-03, Vol.28 (5), p.638-638

Osterziel, Karl Josef

2007

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A Systematic Meta-Analysis of the Efficacy and Heterogeneity of Disease Management Programs in Congestive Heart Failure

Journal of cardiac failure, 2006-09, Vol.12 (7), p.554-567

2006

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Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure

Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding

Postextrasystolic regulation patterns of blood pressure and heart rate in patients with idiopathic dilated cardiomyopathy

Measurement of left ventricular dimensions and function in patients with dilated cardiomyopathy

Unequal allelic expression of wild-type and mutated β-myosin in familial hypertrophic cardiomyopathy

DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy

Dysfunction of dysferlin-deficient hearts

A network against failing hearts—Introducing the German “Competence Network Heart Failure”

Composite polymorphisms in the ryanodine receptor 2 gene associated with arrhythmogenic right ventricular cardiomyopathy

Increased Susceptibility to Complement Attack due to Down-Regulation of Decay-Accelerating Factor/CD55 in Dysferlin-Deficient Muscular Dystrophy

Bisoprolol vs. carvedilol in elderly patients with heart failure: rationale and design of the CIBIS-ELD trial

Die arrhythmogene rechtsventrikuläre Kardiomyopathie

Advanced analysis of spontaneous baroreflex sensitivity, blood pressure and heart rate variability in patients with dilated cardiomyopathy

Hypertrophic cardiomyopathy-related beta-myosin mutations cause highly variable calcium sensitivity with functional imbalances among individual muscle cells

Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: Demand for strategies in the management of presymptomatic lamin A/C mutant carriers

A rapid protocol for cardiac troponin T gene mutation detection in familial hypertrophic cardiomyopathy

Cardiac energetics correlates to myocardial hypertrophy in Friedreich's ataxia

The G-231A Polymorphism in the Endothelin-A Receptor Gene Is Associated With Lower Aortic Pressure in Patients With Dilated Cardiomyopathy

Growth Hormone Treatment in Dilated Cardiomyopathy

Angiotensin-Converting Enzyme and Heart Chymase gene Polymorphisms in Hypertrophic Cardiomyopathy

Uric acid and survival in chronic heart failure: Validation and application in metabolic, functional, and hemodynamic staging

Fabry disease: focus on cardiac manifestations and molecular mechanisms

Dilated cardiomyopathy: more genes means more phenotypes

Improved clinical outcome after intracoronary administration of bone-marrow-derived progenitor cells in acute myocardial infarction: final 1 year results of the REPAIR-AMI trial

A Systematic Meta-Analysis of the Efficacy and Heterogeneity of Disease Management Programs in Congestive Heart Failure

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