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Elisabeth M Lodder

Showing results (41-50 of 62) with videos related to

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Plos One|April 28, 2020
Correction: Seasonality of ventricular fibrillation at first myocardial infarction and association with viral exposureCharlotte Glinge, Thomas Engstrøm, Sofie E Midgley, et al.
Plos One|February 27, 2020
Seasonality of ventricular fibrillation at first myocardial infarction and association with viral exposureCharlotte Glinge, Thomas Engstrøm, Sofie E Midgley, et al.
Journal of the American College of Cardiology|August 23, 2014
HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathyAnnalisa Milano, Alexa M C Vermeer, Elisabeth M Lodder, et al.
Journal of the American College of Cardiology|December 3, 2013
Coxsackie and adenovirus receptor is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemiaRoos F J Marsman, Connie R Bezzina, Fabian Freiberg, et al.
Human Molecular Genetics|October 21, 2022
Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetranceJaël S Copier, Marianne Bootsma, Chai A Ng, et al.
Circulation Research|June 7, 2021
Targeting the Microtubule EB1-CLASP2 Complex Modulates Na<sub>V</sub>1.5 at Intercalated DiscsGerard A Marchal, Mariam Jouni, David Y Chiang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2021
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologiesFrancesco Mazzarotto, Megan H Hawley, Matteo Beltrami, et al.
Circulation. Genomic and Precision Medicine|May 18, 2023
Genetic Burden of <i>TNNI3K</i> in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular ArrhythmiasCaroline Pham, Karolina Andrzejczyk, Sean J Jurgens, et al.
Nature Communications|March 14, 2019
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactylyNajim Lahrouchi, Aman George, Ilham Ratbi, et al.
Journal of the American College of Cardiology|April 29, 2017
Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death SyndromeNajim Lahrouchi, Hariharan Raju, Elisabeth M Lodder, et al.
Pageof 7

Showing results (41-50 of 62) with videos related to

Sort By:
Pageof 7
Plos One|April 28, 2020
Correction: Seasonality of ventricular fibrillation at first myocardial infarction and association with viral exposureCharlotte Glinge, Thomas Engstrøm, Sofie E Midgley, et al.
Plos One|February 27, 2020
Seasonality of ventricular fibrillation at first myocardial infarction and association with viral exposureCharlotte Glinge, Thomas Engstrøm, Sofie E Midgley, et al.
Journal of the American College of Cardiology|August 23, 2014
HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathyAnnalisa Milano, Alexa M C Vermeer, Elisabeth M Lodder, et al.
Journal of the American College of Cardiology|December 3, 2013
Coxsackie and adenovirus receptor is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemiaRoos F J Marsman, Connie R Bezzina, Fabian Freiberg, et al.
Human Molecular Genetics|October 21, 2022
Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetranceJaël S Copier, Marianne Bootsma, Chai A Ng, et al.
Circulation Research|June 7, 2021
Targeting the Microtubule EB1-CLASP2 Complex Modulates Na<sub>V</sub>1.5 at Intercalated DiscsGerard A Marchal, Mariam Jouni, David Y Chiang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2021
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologiesFrancesco Mazzarotto, Megan H Hawley, Matteo Beltrami, et al.
Circulation. Genomic and Precision Medicine|May 18, 2023
Genetic Burden of <i>TNNI3K</i> in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular ArrhythmiasCaroline Pham, Karolina Andrzejczyk, Sean J Jurgens, et al.
Nature Communications|March 14, 2019
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactylyNajim Lahrouchi, Aman George, Ilham Ratbi, et al.
Journal of the American College of Cardiology|April 29, 2017
Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death SyndromeNajim Lahrouchi, Hariharan Raju, Elisabeth M Lodder, et al.
Pageof 7