H. Wedekind

发表

KCNE1 mutations cause Jervell and Lange-Nielsen syndrome

G. Breithardt, W. Haverkamp, J. Towbin, 1997, Nature Genetics.

A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype

G. Breithardt, W. Haverkamp, E. Schulze-Bahr, 2001, Journal of Molecular Medicine.

Implantable cardioverter-defibrillator therapy in patients with congenital long-QT syndrome: a long-term follow-up.

G. Breithardt, H. Scheld, P. Milberg, 2005, Heart rhythm.

Genetics of Sinus Node Disease

G. Breithardt, E. Schulze-Bahr, H. Wedekind, 2004 .

Cardiac arrhythmias and sudden death in infancy: implication for the medicolegal investigation

G. Breithardt, E. Schulze-Bahr, H. Wedekind, 2007, International Journal of Legal Medicine.

Angeborene QT-Syndrome

G. Breithardt, G. Mönnig, W. Haverkamp, 2002, Herzschrittmachertherapie und Elektrophysiologie.

Haverkamp Angeborene QT-Syndrome Diagnostik und Genetik

G. Breithardt, W., G. Mönnig, 2002 .

Molecular impact of ion channel mutations for the pathogenesis of long-QT (LQT) syndromes

G. Breithardt, W. Haverkamp, M. Borggrefe, 2000 .

Rapid, Sensitive Detection of Mutant Alleles in Codon 12 of K -ra s by REMS-PCR

W. Haverkamp, M. Borggrefe, E. Schulze-Bahr, 1999 .

Molecular diagnosis in a child with sudden infant death syndrome

G. Breithardt, S. Priori, P. Schwartz, 2001, The Lancet.

De Novo Mutation in the SCN5A Gene Associated With Early Onset of Sudden Infant Death

G. Breithardt, W. Haverkamp, M. Borggrefe, 2001, Circulation.

Acquired abnormal QT prolongation and torsade de pointes — clinical significance of genetic information from congenital long QT syndrome

G. Breithardt, P. Kirchhof, G. Mönnig, 2000 .

Mapping of a gene for familial juvenile nephronophthisis: refining the map and defining flanking markers on chromosome 2. APN Study Group.

H. Omran, C. Antignac, F. Hildebrandt, 1993, American journal of human genetics.

Sudden Infant Death Syndrome and Long-QT Syndrome: What is Their Relationship?

G. Breithardt, H. Wedekind, 2000 .

Resolution of left atrial appendage thrombi: No difference between phenprocoumon and non‐vitamin K‐dependent oral antagonists

L. Eckardt, H. Wedekind, H. Findeisen, 2022, Clinical cardiology.

PET-CT imaging in the diagnosis of coronary stent infection

H. Wedekind, P. Matheja, Ulrich Großekettler, 2013, Journal of Nuclear Cardiology.

Effective long‐term control of cardiac events with β‐blockers in a family with a common LQT1 mutation

G. Breithardt, W. Haverkamp, E. Schulze-Bahr, 2004, Clinical genetics.

Genetic aspects in acquired long QT syndrome — a piece in the puzzle

G. Breithardt, P. Kirchhof, W. Haverkamp, 2001 .

Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome.

A. Wilde, E. Schulze-Bahr, C. Bezzina, 2005, Cardiovascular research.

Pathological changes of the heart in sudden infant death

H. Wedekind, B. Brinkmann, T. Bajanowski, 2003, International Journal of Legal Medicine.

Clinical Value of Electrocardiographic Parameters in Genotyped Individuals with Familial Long QT Syndrome

G. Breithardt, P. Kirchhof, W. Haverkamp, 2001, Pacing and clinical electrophysiology : PACE.

Electrocardiographic risk stratification in families with congenital long QT syndrome.

G. Breithardt, P. Kirchhof, P. Milberg, 2006, European heart journal.

Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous

G. Breithardt, W. Haverkamp, M. Borggrefe, 1997, Human Genetics.

Clinical aspects of ventricular arrhythmias associated with QT prolongation

G. Breithardt, P. Kirchhof, G. Mönnig, 2001 .

Prolonged QT interval and sudden infant death--report of two cases.

W. Haverkamp, H. Wedekind, B. Brinkmann, 2001, Forensic science international.

QT interval prolongation and risk for cardiac events in genotyped LQTS-index children

G. Breithardt, G. Mönnig, E. Schulze-Bahr, 2009, European Journal of Pediatrics.

Prolonged Atrial Action Potential Durations and Polymorphic Atrial Tachyarrhythmias in Patients with Long QT Syndrome

G. Breithardt, P. Kirchhof, G. Mönnig, 2003, Journal of cardiovascular electrophysiology.

Molecular genetics of arrhythmias – a new paradigm

W. Haverkamp, G. Breithardt, M. Borggrefe, 2000, Zeitschrift für Kardiologie.

The LQT syndromes – current status of molecular mechanisms

W. Haverkamp, G. Breithardt, M. Borggrefe, 1999, Zeitschrift für Kardiologie.

The long QT syndrome: Considerations in the athletic population

Lars Eckardt, Günter Breithardt, Eric Schulze-Bahr, 2003, Current sports medicine reports.

Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study

Bernd Brinkmann, Thomas Bajanowski, Günter Breithardt, 2006, International Journal of Legal Medicine.

Long QT syndrome and life threatening arrhythmia in a newborn: molecular diagnosis and treatment response

G. Breithardt, G. Mönnig, W. Haverkamp, 2003, Heart.

Postextrasystolic “T wave hump” augmentation as a marker of increased arrhythmogenic risk in the long QT syndrome

E. Schulze-Bahr, H. Wedekind, H. Djonlagić, 2002, Heart.

Gene for Familial Juvenile Nephronophthisis: Refining the Map and Defining Flanking Markers

H. Omran, C. Antignac, F. Hildebrandt, 2006 .

The long QT syndrome: Considerations in the athletic population

G. Breithardt, G. Mönnig, L. Eckardt, 2003, Current sports medicine reports.