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Luca Brunelli

Showing results (41-50 of 55) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 9, 2023
Provision and availability of genomic medicine services in Level IV neonatal intensive care unitsMonica H Wojcik, Katharine P Callahan, Austin Antoniou, et al.
Journal of Clinical and Translational Science|December 1, 2021
Addressing ethical and laboratory challenges for initiation of a rapid whole genome sequencing programSabrina Malone Jenkins, Rachel Palmquist, Ashley L Kapron, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|May 28, 2026
Efficacy of universal genome sequencing in infant extracorporeal membrane oxygenationNicholas R Carr, Makenzie L Fulmer, Jennifer Rumpel, et al.
Gene|December 26, 2012
14-3-3ε gene variants in a Japanese patient with left ventricular noncompaction and hypoplasia of the corpus callosumBo Chang, Carlos Gorbea, George Lezin, et al.
Circulation. Arrhythmia and Electrophysiology|August 30, 2012
Loss of function of hNav1.5 by a ZASP1 mutation associated with intraventricular conduction disturbances in left ventricular noncompactionYutao Xi, Tomohiko Ai, Enno De Lange, et al.
Circulation. Arrhythmia and Electrophysiology|September 21, 2010
A ZASP missense mutation, S196L, leads to cytoskeletal and electrical abnormalities in a mouse model of cardiomyopathyZhaohui Li, Tomohiko Ai, Kaveh Samani, et al.
Studies in Health Technology and Informatics|May 12, 2023
Impact of Professional Background on Inter-Annotator Variability and Accuracy During Annotation of Clinical NotesKristina Weishäupl, Mario Schuster, Christina Mayrl, et al.
International Journal of Cardiology. Heart & Vasculature|December 30, 2025
Assisted therapy optimizing module to improve physician adhErence with guideLine-directed medical heart failure therapy rationale and design of the AMPEL trialLuca Brunelli, Luiza Hoch, Bernhard Pfeifer, et al.
Pediatric Research|February 4, 2022
Evaluating use of changing technologies for rapid next-generation sequencing in pediatricsRachel Palmquist, Sabrina Malone Jenkins, Dawn Bentley, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic herniaCammon B Arrington, Steven B Bleyl, Nori Matsunami, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 9, 2023
Provision and availability of genomic medicine services in Level IV neonatal intensive care unitsMonica H Wojcik, Katharine P Callahan, Austin Antoniou, et al.
Journal of Clinical and Translational Science|December 1, 2021
Addressing ethical and laboratory challenges for initiation of a rapid whole genome sequencing programSabrina Malone Jenkins, Rachel Palmquist, Ashley L Kapron, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|May 28, 2026
Efficacy of universal genome sequencing in infant extracorporeal membrane oxygenationNicholas R Carr, Makenzie L Fulmer, Jennifer Rumpel, et al.
Gene|December 26, 2012
14-3-3ε gene variants in a Japanese patient with left ventricular noncompaction and hypoplasia of the corpus callosumBo Chang, Carlos Gorbea, George Lezin, et al.
Circulation. Arrhythmia and Electrophysiology|August 30, 2012
Loss of function of hNav1.5 by a ZASP1 mutation associated with intraventricular conduction disturbances in left ventricular noncompactionYutao Xi, Tomohiko Ai, Enno De Lange, et al.
Circulation. Arrhythmia and Electrophysiology|September 21, 2010
A ZASP missense mutation, S196L, leads to cytoskeletal and electrical abnormalities in a mouse model of cardiomyopathyZhaohui Li, Tomohiko Ai, Kaveh Samani, et al.
Studies in Health Technology and Informatics|May 12, 2023
Impact of Professional Background on Inter-Annotator Variability and Accuracy During Annotation of Clinical NotesKristina Weishäupl, Mario Schuster, Christina Mayrl, et al.
International Journal of Cardiology. Heart & Vasculature|December 30, 2025
Assisted therapy optimizing module to improve physician adhErence with guideLine-directed medical heart failure therapy rationale and design of the AMPEL trialLuca Brunelli, Luiza Hoch, Bernhard Pfeifer, et al.
Pediatric Research|February 4, 2022
Evaluating use of changing technologies for rapid next-generation sequencing in pediatricsRachel Palmquist, Sabrina Malone Jenkins, Dawn Bentley, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic herniaCammon B Arrington, Steven B Bleyl, Nori Matsunami, et al.
Pageof 6