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Elisabeth M Lodder

Showing results (31-40 of 62) with videos related to

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Disease Models & Mechanisms|June 19, 2019
Genetic variation in <i>GNB5</i> causes bradycardia by augmenting the cholinergic response via increased acetylcholine-activated potassium current (<i>I</i><sub>K,ACh</sub>)Christiaan C Veerman, Isabella Mengarelli, Charlotte D Koopman, et al.
JAMA Network Open|January 25, 2023
Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in DenmarkCharlotte Glinge, Sára Rossetti, Louise Bruun Oestergaard, et al.
Circulation Research|June 23, 2017
The Brugada Syndrome Susceptibility Gene <i>HEY2</i> Modulates Cardiac Transmural Ion Channel Patterning and Electrical HeterogeneityChristiaan C Veerman, Svitlana Podliesna, Rafik Tadros, et al.
Plos One|May 22, 2014
Genome-wide identification of expression quantitative trait loci (eQTLs) in human heartTamara T Koopmann, Michiel E Adriaens, Perry D Moerland, et al.
Journal of the American College of Cardiology|May 14, 2016
Dilation of the Aorta Ascendens Forms Part of the Clinical Spectrum of HCN4 MutationsAlexa M C Vermeer, Elisabeth M Lodder, Dierk Thomas, et al.
Plos One|November 17, 2020
Histological, immunohistochemical and transcriptomic characterization of human tracheoesophageal fistulasErwin Brosens, Janine F Felix, Anne Boerema-de Munck, et al.
Open Heart|February 6, 2021
Discovery of predictors of sudden cardiac arrest in diabetes: rationale and outline of the RESCUED (REcognition of Sudden Cardiac arrest vUlnErability in Diabetes) projectLaura H van Dongen, Peter P Harms, Mark Hoogendoorn, et al.
Heart Rhythm|July 17, 2018
Supraventricular tachycardias, conduction disease, and cardiomyopathy in 3 families with the same rare variant in TNNI3K (p.Glu768Lys)Svitlana Podliesna, Julian Delanne, Lindsey Miller, et al.
American Journal of Medical Genetics. Part A|July 14, 2019
GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrumDoris Škorić-Milosavljević, Fleur V Y Tjong, Julien Barc, et al.
The New England Journal of Medicine|November 1, 2018
A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment DepressionHenning Bundgaard, Christian Jøns, Elisabeth M Lodder, et al.
Pageof 7

Showing results (31-40 of 62) with videos related to

Sort By:
Pageof 7
Disease Models & Mechanisms|June 19, 2019
Genetic variation in <i>GNB5</i> causes bradycardia by augmenting the cholinergic response via increased acetylcholine-activated potassium current (<i>I</i><sub>K,ACh</sub>)Christiaan C Veerman, Isabella Mengarelli, Charlotte D Koopman, et al.
JAMA Network Open|January 25, 2023
Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in DenmarkCharlotte Glinge, Sára Rossetti, Louise Bruun Oestergaard, et al.
Circulation Research|June 23, 2017
The Brugada Syndrome Susceptibility Gene <i>HEY2</i> Modulates Cardiac Transmural Ion Channel Patterning and Electrical HeterogeneityChristiaan C Veerman, Svitlana Podliesna, Rafik Tadros, et al.
Plos One|May 22, 2014
Genome-wide identification of expression quantitative trait loci (eQTLs) in human heartTamara T Koopmann, Michiel E Adriaens, Perry D Moerland, et al.
Journal of the American College of Cardiology|May 14, 2016
Dilation of the Aorta Ascendens Forms Part of the Clinical Spectrum of HCN4 MutationsAlexa M C Vermeer, Elisabeth M Lodder, Dierk Thomas, et al.
Plos One|November 17, 2020
Histological, immunohistochemical and transcriptomic characterization of human tracheoesophageal fistulasErwin Brosens, Janine F Felix, Anne Boerema-de Munck, et al.
Open Heart|February 6, 2021
Discovery of predictors of sudden cardiac arrest in diabetes: rationale and outline of the RESCUED (REcognition of Sudden Cardiac arrest vUlnErability in Diabetes) projectLaura H van Dongen, Peter P Harms, Mark Hoogendoorn, et al.
Heart Rhythm|July 17, 2018
Supraventricular tachycardias, conduction disease, and cardiomyopathy in 3 families with the same rare variant in TNNI3K (p.Glu768Lys)Svitlana Podliesna, Julian Delanne, Lindsey Miller, et al.
American Journal of Medical Genetics. Part A|July 14, 2019
GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrumDoris Škorić-Milosavljević, Fleur V Y Tjong, Julien Barc, et al.
The New England Journal of Medicine|November 1, 2018
A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment DepressionHenning Bundgaard, Christian Jøns, Elisabeth M Lodder, et al.
Pageof 7