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A A Wilde

Showing results (71-80 of 78) with videos related to

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Human Mutation|April 29, 1999
Novel KCNQ1 and HERG missense mutations in Dutch long-QT familiesR J Jongbloed, A A Wilde, J L Geelen, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Cardiac involvement in carriers of Duchenne and Becker muscular dystrophyE M Hoogerwaard, P A van der Wouw, A A Wilde, et al.
Lancet (London, England)|June 26, 1999
Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort studyE M Hoogerwaard, E Bakker, P F Ippel, et al.
Journal of Cardiovascular Electrophysiology|June 19, 2001
Possible bradycardic mode of death and successful pacemaker treatment in a large family with features of long QT syndrome type 3 and Brugada syndromeM P van den Berg, A A Wilde, Viersma TJW, et al.
Heart (British Cardiac Society)|July 22, 2009
Persistent precordial "hyperacute" T-waves signify proximal left anterior descending artery occlusionN J Verouden, K T Koch, R J Peters, et al.
Circulation Research|December 11, 1999
A single Na(+) channel mutation causing both long-QT and Brugada syndromesC Bezzina, M W Veldkamp, M P van Den Berg, et al.
Neuromuscular Disorders : NMD|April 3, 2018
Prevalence and mutation spectrum of skeletal muscle channelopathies in the NetherlandsB C Stunnenberg, J Raaphorst, J C W Deenen, et al.
Circulation|January 4, 2001
Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmiasP J Schwartz, S G Priori, C Spazzolini, et al.
Pageof 8

Showing results (71-80 of 78) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 78 results.
Human Mutation|April 29, 1999
Novel KCNQ1 and HERG missense mutations in Dutch long-QT familiesR J Jongbloed, A A Wilde, J L Geelen, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Cardiac involvement in carriers of Duchenne and Becker muscular dystrophyE M Hoogerwaard, P A van der Wouw, A A Wilde, et al.
Lancet (London, England)|June 26, 1999
Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort studyE M Hoogerwaard, E Bakker, P F Ippel, et al.
Journal of Cardiovascular Electrophysiology|June 19, 2001
Possible bradycardic mode of death and successful pacemaker treatment in a large family with features of long QT syndrome type 3 and Brugada syndromeM P van den Berg, A A Wilde, Viersma TJW, et al.
Heart (British Cardiac Society)|July 22, 2009
Persistent precordial "hyperacute" T-waves signify proximal left anterior descending artery occlusionN J Verouden, K T Koch, R J Peters, et al.
Circulation Research|December 11, 1999
A single Na(+) channel mutation causing both long-QT and Brugada syndromesC Bezzina, M W Veldkamp, M P van Den Berg, et al.
Neuromuscular Disorders : NMD|April 3, 2018
Prevalence and mutation spectrum of skeletal muscle channelopathies in the NetherlandsB C Stunnenberg, J Raaphorst, J C W Deenen, et al.
Circulation|January 4, 2001
Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmiasP J Schwartz, S G Priori, C Spazzolini, et al.
Pageof 8