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X-chromosome inactivation in female patients with Fabry disease

Clinical genetics, 2016-01, Vol.89 (1), p.44-54

2016

Volltextzugriff (PDF)

Skeletal myoblast transplantation in ischemic heart failure : Long-term follow-up of the first phase I cohort of patients

Circulation (New York, N.Y.), 2006-07, Vol.114 (1), p.I108-I113

2006

Volltextzugriff (PDF)

Screening patients with hypertrophic cardiomyopathy for Fabry disease using a filter-paper test: the FOCUS study

Heart (British Cardiac Society), 2011-01, Vol.97 (2), p.131-136

2011

Volltextzugriff (PDF)

Serial left ventricular adaptations in world-class professional cyclists: implications for disease screening and follow-up

Journal of the American College of Cardiology, 2004-07, Vol.44 (1), p.144-149

2004

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XANTUS: a real-world, prospective, observational study of patients treated with rivaroxaban for stroke prevention in atrial fibrillation

European heart journal, 2016-04, Vol.37 (14), p.1145-1153

2016

Volltextzugriff (PDF)

Preeminence of Staphylococcus aureus in Infective Endocarditis: A 1-Year Population-Based Survey

Clinical infectious diseases, 2012-05, Vol.54 (9), p.1230-1239

2012

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Double heterozygosity for mutations in the β-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy

Journal of medical genetics, 1999-07, Vol.36 (7), p.542-545

1999

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Percutaneous transluminal septal coil embolisation as an alternative to alcohol septal ablation for hypertrophic obstructive cardiomyopathy

Heart (British Cardiac Society), 2005-01, Vol.91 (1), p.92-92

2005

Volltextzugriff (PDF)

Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy

Circulation (New York, N.Y.), 1996-12, Vol.94 (12), p.3069-3073

1996

Volltextzugriff (PDF)

Detection of Pathologic or Physiologic Left Ventricular Remodeling in Athletes

Journal of the American College of Cardiology, 2005-05, Vol.45 (10), p.1731-1731

2005

Volltextzugriff (PDF)

Prognostic value of skin manifestations of infective endocarditis

JAMA dermatology (Chicago, Ill.), 2014-05, Vol.150 (5), p.494

2014

Volltextzugriff (PDF)

Relation between QT duration and maximal wall thickness in familial hypertrophic cardiomyopathy

Heart (British Cardiac Society), 2002-08, Vol.88 (2), p.153-157

2002

Volltextzugriff (PDF)

Peptic ulcer disease: one in five is related to neither Helicobacter pylori nor aspirin/NSAID intake

Alimentary pharmacology & therapeutics, 2013-10, Vol.38 (8), p.946-954

2013

Volltextzugriff (PDF)

Familial hypertrophic cardiomyopathy. Cardiac ultrasonic abnormalities in genetically affected subjects without echocardiographic evidence of left ventricular hypertrophy

European heart journal, 1998-03, Vol.19 (3), p.490-499

1998

Volltextzugriff (PDF)

Accuracy of European diagnostic criteria for familial hypertrophic cardiomyopathy in a genotyped population

International journal of cardiology, 2003-07, Vol.90 (1), p.33-38

2003

Volltextzugriff (PDF)

Favorable Prognosis of Upper-Gastrointestinal Bleeding in 1041 Older Patients: Results of a Prospective Multicenter Study

Clinical gastroenterology and hepatology, 2008-08, Vol.6 (8), p.886-892

2008

Volltextzugriff (PDF)

Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse

European heart journal, 2022-05, Vol.43 (17), p.1668-1680

2022

Volltextzugriff (PDF)

Autologous skeletal myoblast transplantation for severe postinfarction left ventricular dysfunction

Journal of the American College of Cardiology, 2003-04, Vol.41 (7), p.1078-1083

2003

Volltextzugriff (PDF)

Preliminary report: follow-up after dynamic cardiomyoplasty

The Lancet (British edition), 1990-05, Vol.335 (8698), p.1122-1124

1990

Volltextzugriff (PDF)

Aficamten for Symptomatic Obstructive Hypertrophic Cardiomyopathy

The New England journal of medicine, 2024-05, Vol.390 (20), p.1849

2024

Volltextzugriff (PDF)

Acute hepatitis C: analysis of a 126-case prospective, multicenter cohort

European journal of gastroenterology & hepatology, 2010-02, Vol.22 (2), p.157-166

2010

Volltextzugriff (PDF)

Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene

Circulation (New York, N.Y.), 1998-06, Vol.97 (22), p.2230-2236

1998

Volltextzugriff (PDF)

“Crochetage” (Notch) on R wave in inferior limb leads: A new independent electrocardiographic sign of atrial septal defect

Journal of the American College of Cardiology, 1996-03, Vol.27 (4), p.877-882

1996

Volltextzugriff (PDF)

Clinical study of the effects of latissimus dorsi muscle flap stimulation after cardiomyoplasty

Circulation (New York, N.Y.), 1995-11, Vol.92 (9 Suppl), p.II210-215

1995

Volltextzugriff (PDF)

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X-chromosome inactivation in female patients with Fabry disease

Skeletal myoblast transplantation in ischemic heart failure : Long-term follow-up of the first phase I cohort of patients

Screening patients with hypertrophic cardiomyopathy for Fabry disease using a filter-paper test: the FOCUS study

Serial left ventricular adaptations in world-class professional cyclists: implications for disease screening and follow-up

2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC)

XANTUS: a real-world, prospective, observational study of patients treated with rivaroxaban for stroke prevention in atrial fibrillation

Preeminence of Staphylococcus aureus in Infective Endocarditis: A 1-Year Population-Based Survey

Double heterozygosity for mutations in the β-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy

Percutaneous transluminal septal coil embolisation as an alternative to alcohol septal ablation for hypertrophic obstructive cardiomyopathy

Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy

Detection of Pathologic or Physiologic Left Ventricular Remodeling in Athletes

Prognostic value of skin manifestations of infective endocarditis

Relation between QT duration and maximal wall thickness in familial hypertrophic cardiomyopathy

Peptic ulcer disease: one in five is related to neither Helicobacter pylori nor aspirin/NSAID intake

Familial hypertrophic cardiomyopathy. Cardiac ultrasonic abnormalities in genetically affected subjects without echocardiographic evidence of left ventricular hypertrophy

Accuracy of European diagnostic criteria for familial hypertrophic cardiomyopathy in a genotyped population

Favorable Prognosis of Upper-Gastrointestinal Bleeding in 1041 Older Patients: Results of a Prospective Multicenter Study

Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse

Autologous skeletal myoblast transplantation for severe postinfarction left ventricular dysfunction

Preliminary report: follow-up after dynamic cardiomyoplasty

Aficamten for Symptomatic Obstructive Hypertrophic Cardiomyopathy

Acute hepatitis C: analysis of a 126-case prospective, multicenter cohort

Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene

“Crochetage” (Notch) on R wave in inferior limb leads: A new independent electrocardiographic sign of atrial septal defect

Clinical study of the effects of latissimus dorsi muscle flap stimulation after cardiomyoplasty

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