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M J Ackerman

Showing results (51-60 of 57) with videos related to

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Journal of Molecular and Cellular Cardiology|September 1, 2000
Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathyT M Olson, T P Doan, N Y Kishimoto, et al.
Neurology|November 29, 2008
Identification of a possible pathogenic link between congenital long QT syndrome and epilepsyJ N Johnson, N Hofman, C M Haglund, et al.
Heart (British Cardiac Society)|March 14, 2009
Device complications and inappropriate implantable cardioverter defibrillator shocks in patients with hypertrophic cardiomyopathyG Lin, R A Nishimura, B J Gersh, et al.
Pediatric Research|August 14, 1998
A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's familyM J Ackerman, J J Schroeder, R Berry, et al.
The Journal of Thoracic and Cardiovascular Surgery|July 4, 2001
Pulmonary atresia with ventricular septal defect and persistent airway hyperresponsivenessM J Ackerman, M E Wylam, R H Feldt, et al.
JAMA|November 17, 2001
Postmortem molecular analysis of SCN5A defects in sudden infant death syndromeM J Ackerman, B L Siu, W Q Sturner, et al.
Neurogastroenterology and Motility|October 3, 2002
SCN5A is expressed in human jejunal circular smooth muscle cellsY Ou, S J Gibbons, S M Miller, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Journal of Molecular and Cellular Cardiology|September 1, 2000
Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathyT M Olson, T P Doan, N Y Kishimoto, et al.
Neurology|November 29, 2008
Identification of a possible pathogenic link between congenital long QT syndrome and epilepsyJ N Johnson, N Hofman, C M Haglund, et al.
Heart (British Cardiac Society)|March 14, 2009
Device complications and inappropriate implantable cardioverter defibrillator shocks in patients with hypertrophic cardiomyopathyG Lin, R A Nishimura, B J Gersh, et al.
Pediatric Research|August 14, 1998
A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's familyM J Ackerman, J J Schroeder, R Berry, et al.
The Journal of Thoracic and Cardiovascular Surgery|July 4, 2001
Pulmonary atresia with ventricular septal defect and persistent airway hyperresponsivenessM J Ackerman, M E Wylam, R H Feldt, et al.
JAMA|November 17, 2001
Postmortem molecular analysis of SCN5A defects in sudden infant death syndromeM J Ackerman, B L Siu, W Q Sturner, et al.
Neurogastroenterology and Motility|October 3, 2002
SCN5A is expressed in human jejunal circular smooth muscle cellsY Ou, S J Gibbons, S M Miller, et al.
Pageof 6