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J Ackerman

Showing results (181-190 of 1,428) with videos related to

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Circulation Research|August 21, 2010
Defining a new paradigm for human arrhythmia syndromes: phenotypic manifestations of gene mutations in ion channel- and transporter-associated proteinsMichael J Ackerman, Peter J Mohler
Annual Review of Medicine|October 22, 2008
Cardiomyopathic and channelopathic causes of sudden unexplained death in infants and childrenDavid J Tester, Michael J Ackerman
Nature Reviews. Cardiology|February 1, 2012
Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapyJohn R Giudicessi, Michael J Ackerman
Circulation|December 8, 2010
Mutation type is not clinically useful in predicting prognosis in hypertrophic cardiomyopathyAndrew P Landstrom, Michael J Ackerman
Clinical Pharmacology and Therapeutics|September 22, 2011
The Achilles' heel of cardiovascular genetic testing: distinguishing pathogenic mutations from background genetic noiseA P Landstrom, M J Ackerman
The Journal of Biological Chemistry|October 5, 1990
Ribozymes correctly cleave a model substrate and endogenous RNA in vivoS K Saxena, E J Ackerman
Research in Developmental Disabilities|January 1, 1993
Who is treated using restrictive behavioral procedures? A population perspectiveJ W Jacobson, L J Ackerman
Journal of Neurosurgery. Spine|May 9, 2014
ResponseStacey J Ackerman, David W Polly
Circulation. Cardiovascular Genetics|August 22, 2013
Arrhythmia risk in long QT syndrome: beyond the disease-causative mutationJohn R Giudicessi, Michael J Ackerman
Circulation. Genomic and Precision Medicine|March 14, 2020
Established Loss-of-Function Variants in <i>ANK2</i>-Encoded Ankyrin-B Rarely Cause a Concerning Cardiac Phenotype in HumansJohn R Giudicessi, Michael J Ackerman
Pageof 143

Showing results (181-190 of 1,428) with videos related to

Sort By:
Pageof 143
Circulation Research|August 21, 2010
Defining a new paradigm for human arrhythmia syndromes: phenotypic manifestations of gene mutations in ion channel- and transporter-associated proteinsMichael J Ackerman, Peter J Mohler
Annual Review of Medicine|October 22, 2008
Cardiomyopathic and channelopathic causes of sudden unexplained death in infants and childrenDavid J Tester, Michael J Ackerman
Nature Reviews. Cardiology|February 1, 2012
Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapyJohn R Giudicessi, Michael J Ackerman
Circulation|December 8, 2010
Mutation type is not clinically useful in predicting prognosis in hypertrophic cardiomyopathyAndrew P Landstrom, Michael J Ackerman
Clinical Pharmacology and Therapeutics|September 22, 2011
The Achilles' heel of cardiovascular genetic testing: distinguishing pathogenic mutations from background genetic noiseA P Landstrom, M J Ackerman
The Journal of Biological Chemistry|October 5, 1990
Ribozymes correctly cleave a model substrate and endogenous RNA in vivoS K Saxena, E J Ackerman
Research in Developmental Disabilities|January 1, 1993
Who is treated using restrictive behavioral procedures? A population perspectiveJ W Jacobson, L J Ackerman
Journal of Neurosurgery. Spine|May 9, 2014
ResponseStacey J Ackerman, David W Polly
Circulation. Cardiovascular Genetics|August 22, 2013
Arrhythmia risk in long QT syndrome: beyond the disease-causative mutationJohn R Giudicessi, Michael J Ackerman
Circulation. Genomic and Precision Medicine|March 14, 2020
Established Loss-of-Function Variants in <i>ANK2</i>-Encoded Ankyrin-B Rarely Cause a Concerning Cardiac Phenotype in HumansJohn R Giudicessi, Michael J Ackerman
Pageof 143