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Matteo Vatta

Showing results (111-120 of 124) with videos related to

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Plos One|September 22, 2017
Clinical characteristics and 12-month outcomes of patients with valvular and non-valvular atrial fibrillation in KenyaTecla M Temu, Kathleen A Lane, Changyu Shen, et al.
Neuromuscular Disorders : NMD|December 24, 2023
A recurrent ACTA1 amino acid change in mosaic form causes milder asymmetric myopathyVilma-Lotta Lehtokari, Lydia Sagath, Mark Davis, et al.
Journal of the American College of Cardiology|February 16, 2010
Compound and digenic heterozygosity contributes to arrhythmogenic right ventricular cardiomyopathyTianhong Xu, Zhao Yang, Matteo Vatta, et al.
American Journal of Physiology. Heart and Circulatory Physiology|April 21, 2018
Ondansetron blocks wild-type and p.F503L variant small-conductance Ca<sup>2+</sup>-activated K<sup>+</sup> channelsJum-Suk Ko, Shuai Guo, Jonathan Hassel, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 4, 2015
Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199Bryan P Schneider, Lang Li, Milan Radovich, et al.
Journal of the American College of Cardiology|December 10, 2003
Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compactionMatteo Vatta, Bhagyalaxmi Mohapatra, Shinawe Jimenez, et al.
Human Mutation|June 10, 2020
An assessment of the role of vinculin loss of function variants in inherited cardiomyopathyMegan H Hawley, Naif Almontashiri, Leslie G Biesecker, et al.
Human Molecular Genetics|December 26, 2016
MIB2 variants altering NOTCH signalling result in left ventricle hypertrabeculation/non-compaction and are associated with Ménétrier-like gastropathyPasquale Piccolo, Sergio Attanasio, Ilaria Secco, et al.
Heart Rhythm|February 5, 2010
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testingJamie D Kapplinger, David J Tester, Marielle Alders, et al.
The Journal of Molecular Diagnostics : JMD|February 25, 2021
Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM): A Study from the ClinGen Cardiomyopathy Variant Curation Expert PanelAna Morales, Alexander Ing, Christian Antolik, et al.
Pageof 13

Showing results (111-120 of 124) with videos related to

Sort By:
Pageof 13
Plos One|September 22, 2017
Clinical characteristics and 12-month outcomes of patients with valvular and non-valvular atrial fibrillation in KenyaTecla M Temu, Kathleen A Lane, Changyu Shen, et al.
Neuromuscular Disorders : NMD|December 24, 2023
A recurrent ACTA1 amino acid change in mosaic form causes milder asymmetric myopathyVilma-Lotta Lehtokari, Lydia Sagath, Mark Davis, et al.
Journal of the American College of Cardiology|February 16, 2010
Compound and digenic heterozygosity contributes to arrhythmogenic right ventricular cardiomyopathyTianhong Xu, Zhao Yang, Matteo Vatta, et al.
American Journal of Physiology. Heart and Circulatory Physiology|April 21, 2018
Ondansetron blocks wild-type and p.F503L variant small-conductance Ca<sup>2+</sup>-activated K<sup>+</sup> channelsJum-Suk Ko, Shuai Guo, Jonathan Hassel, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 4, 2015
Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199Bryan P Schneider, Lang Li, Milan Radovich, et al.
Journal of the American College of Cardiology|December 10, 2003
Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compactionMatteo Vatta, Bhagyalaxmi Mohapatra, Shinawe Jimenez, et al.
Human Mutation|June 10, 2020
An assessment of the role of vinculin loss of function variants in inherited cardiomyopathyMegan H Hawley, Naif Almontashiri, Leslie G Biesecker, et al.
Human Molecular Genetics|December 26, 2016
MIB2 variants altering NOTCH signalling result in left ventricle hypertrabeculation/non-compaction and are associated with Ménétrier-like gastropathyPasquale Piccolo, Sergio Attanasio, Ilaria Secco, et al.
Heart Rhythm|February 5, 2010
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testingJamie D Kapplinger, David J Tester, Marielle Alders, et al.
The Journal of Molecular Diagnostics : JMD|February 25, 2021
Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM): A Study from the ClinGen Cardiomyopathy Variant Curation Expert PanelAna Morales, Alexander Ing, Christian Antolik, et al.
Pageof 13