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H Wedekind

Showing results (11-20 of 20) with videos related to

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Zeitschrift Fur Kardiologie|January 11, 2001
[New knowledge in arrhythmogenesis--role of ion channels and genetic aspects]W Haverkamp, L Eckardt, P Kirchhof, et al.
Zeitschrift Fur Kardiologie|May 16, 2000
Molecular genetics of arrhythmias--a new paradigmE Schulze-Bahr, W Haverkamp, M Borggrefe, et al.
Human Genetics|October 28, 1997
Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneousE Schulze-Bahr, W Haverkamp, H Wedekind, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 3, 2001
A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotypeE Schulze-Bahr, M Schwarz, S Hauenschild, et al.
American Journal of Human Genetics|December 1, 1993
Mapping of a gene for familial juvenile nephronophthisis: refining the map and defining flanking markers on chromosome 2. APN Study GroupF Hildebrandt, I Singh-Sawhney, B Schnieders, et al.
Clinical Genetics|February 6, 2004
Effective long-term control of cardiac events with beta-blockers in a family with a common LQT1 mutationH Wedekind, M Schwarz, S Hauenschild, et al.
Zeitschrift Fur Kardiologie|July 23, 2002
[Clinical aspects and molecular genetics of the Jervell- and Lange-Nielsen Syndrome]G Mönnig, E Schulze-Bahr, H Wedekind, et al.
Pacing and Clinical Electrophysiology : PACE|May 9, 2001
Clinical value of electrocardiographic parameters in genotyped individuals with familial long QT syndromeG Moennig, E Schulze-Bahr, H Wedekind, et al.
Lancet (London, England)|October 31, 2001
Molecular diagnosis in a child with sudden infant death syndromeP J Schwartz, S G Priori, R Bloise, et al.
Circulation|September 6, 2001
De novo mutation in the SCN5A gene associated with early onset of sudden infant deathH Wedekind, J P Smits, E Schulze-Bahr, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Zeitschrift Fur Kardiologie|January 11, 2001
[New knowledge in arrhythmogenesis--role of ion channels and genetic aspects]W Haverkamp, L Eckardt, P Kirchhof, et al.
Zeitschrift Fur Kardiologie|May 16, 2000
Molecular genetics of arrhythmias--a new paradigmE Schulze-Bahr, W Haverkamp, M Borggrefe, et al.
Human Genetics|October 28, 1997
Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneousE Schulze-Bahr, W Haverkamp, H Wedekind, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 3, 2001
A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotypeE Schulze-Bahr, M Schwarz, S Hauenschild, et al.
American Journal of Human Genetics|December 1, 1993
Mapping of a gene for familial juvenile nephronophthisis: refining the map and defining flanking markers on chromosome 2. APN Study GroupF Hildebrandt, I Singh-Sawhney, B Schnieders, et al.
Clinical Genetics|February 6, 2004
Effective long-term control of cardiac events with beta-blockers in a family with a common LQT1 mutationH Wedekind, M Schwarz, S Hauenschild, et al.
Zeitschrift Fur Kardiologie|July 23, 2002
[Clinical aspects and molecular genetics of the Jervell- and Lange-Nielsen Syndrome]G Mönnig, E Schulze-Bahr, H Wedekind, et al.
Pacing and Clinical Electrophysiology : PACE|May 9, 2001
Clinical value of electrocardiographic parameters in genotyped individuals with familial long QT syndromeG Moennig, E Schulze-Bahr, H Wedekind, et al.
Lancet (London, England)|October 31, 2001
Molecular diagnosis in a child with sudden infant death syndromeP J Schwartz, S G Priori, R Bloise, et al.
Circulation|September 6, 2001
De novo mutation in the SCN5A gene associated with early onset of sudden infant deathH Wedekind, J P Smits, E Schulze-Bahr, et al.
Pageof 2