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Heart Rhythm
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April 27, 2005
Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome
Anant Khositseth, David J Tester, Melissa L Will, et al.
Mayo Clinic Proceedings
|
May 13, 2005
Pathogenesis of unexplained drowning: new insights from a molecular autopsy
David J Tester, Laura J Kopplin, Wendy Creighton, et al.
Heart Rhythm
|
February 15, 2020
Clinical and functional reappraisal of alleged type 5 long QT syndrome: Causative genetic variants in the KCNE1-encoded minK β-subunit
Ramin Garmany, John R Giudicessi, Dan Ye, et al.
Mayo Clinic Proceedings
|
November 17, 2004
Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases
David J Tester, Daniel B Spoon, Hector H Valdivia, et al.
Heart Rhythm
|
August 14, 2012
Repeat long QT syndrome genetic testing of phenotype-positive cases: prevalence and etiology of detection misses
Morgan M Medlock, David J Tester, Melissa L Will, et al.
Heartrhythm Case Reports
|
January 24, 2022
A novel functional variant residing outside the <i>SCN5A</i>-encoded Na<sub>v</sub>1.5 voltage-sensing domain causes multifocal ectopic Purkinje-related premature contractions
Xiaozhi Gao, Dan Ye, Wei Zhou, et al.
Congenital Heart Disease
|
March 23, 2017
Whole exome sequencing with genomic triangulation implicates CDH2-encoded N-cadherin as a novel pathogenic substrate for arrhythmogenic cardiomyopathy
Kari L Turkowski, David J Tester, J Martijn Bos, et al.
American Journal of Clinical Pathology
|
February 21, 2008
Postmortem genetic testing for conventional autopsy-negative sudden unexplained death: an evaluation of different DNA extraction protocols and the feasibility of mutational analysis from archival paraffin-embedded heart tissue
Elisa Carturan, David J Tester, Brian C Brost, et al.
Mayo Clinic Proceedings
|
June 9, 2012
Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing
David J Tester, Argelia Medeiros-Domingo, Melissa L Will, et al.
Nature Reviews. Cardiology
|
September 8, 2017
Sudden infant death syndrome and inherited cardiac conditions
Alban-Elouen Baruteau, David J Tester, Jamie D Kapplinger, et al.
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of 22
Search research articles
Search
Showing results (41-50 of 212) with videos related to
Sort By:
Page
of 22
Heart Rhythm
|
April 27, 2005
Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome
Anant Khositseth, David J Tester, Melissa L Will, et al.
Mayo Clinic Proceedings
|
May 13, 2005
Pathogenesis of unexplained drowning: new insights from a molecular autopsy
David J Tester, Laura J Kopplin, Wendy Creighton, et al.
Heart Rhythm
|
February 15, 2020
Clinical and functional reappraisal of alleged type 5 long QT syndrome: Causative genetic variants in the KCNE1-encoded minK β-subunit
Ramin Garmany, John R Giudicessi, Dan Ye, et al.
Mayo Clinic Proceedings
|
November 17, 2004
Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases
David J Tester, Daniel B Spoon, Hector H Valdivia, et al.
Heart Rhythm
|
August 14, 2012
Repeat long QT syndrome genetic testing of phenotype-positive cases: prevalence and etiology of detection misses
Morgan M Medlock, David J Tester, Melissa L Will, et al.
Heartrhythm Case Reports
|
January 24, 2022
A novel functional variant residing outside the <i>SCN5A</i>-encoded Na<sub>v</sub>1.5 voltage-sensing domain causes multifocal ectopic Purkinje-related premature contractions
Xiaozhi Gao, Dan Ye, Wei Zhou, et al.
Congenital Heart Disease
|
March 23, 2017
Whole exome sequencing with genomic triangulation implicates CDH2-encoded N-cadherin as a novel pathogenic substrate for arrhythmogenic cardiomyopathy
Kari L Turkowski, David J Tester, J Martijn Bos, et al.
American Journal of Clinical Pathology
|
February 21, 2008
Postmortem genetic testing for conventional autopsy-negative sudden unexplained death: an evaluation of different DNA extraction protocols and the feasibility of mutational analysis from archival paraffin-embedded heart tissue
Elisa Carturan, David J Tester, Brian C Brost, et al.
Mayo Clinic Proceedings
|
June 9, 2012
Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing
David J Tester, Argelia Medeiros-Domingo, Melissa L Will, et al.
Nature Reviews. Cardiology
|
September 8, 2017
Sudden infant death syndrome and inherited cardiac conditions
Alban-Elouen Baruteau, David J Tester, Jamie D Kapplinger, et al.
Page
of 22