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Matteo Vatta

Showing results (21-30 of 124) with videos related to

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European Heart Journal|February 17, 2007
Arrhythmogenic right ventricular cardiomyopathy: a 'final common pathway' that defines clinical phenotypeMatteo Vatta, Frank Marcus, Jeffrey A Towbin
Cardiology in the Young|April 16, 2005
Altered expression of dystrophin within the thoracic aorta in coarctationMatteo Vatta, Anthony C Chang, Colin J McMahon
Journal of Cardiovascular Medicine (Hagerstown, Md.)|February 6, 2009
Remodeling of dystrophin and sarcomeric Z-band occurs in pediatric cardiomyopathies: a unifying mechanism for force transmission defectMatteo Vatta, Gianfranco Sinagra, Luca Brunelli, et al.
Advances in Pediatrics|September 7, 2002
Genetics and cardiac arrhythmiasJeffrey A Towbin, Matteo Vatta, Hua Li, et al.
Circulation Research|February 17, 2007
Peroxisome proliferator-activated receptor-delta upregulates 14-3-3 epsilon in human endothelial cells via CCAAT/enhancer binding protein-betaLuca Brunelli, Katarzyna A Cieslik, Joseph L Alcorn, et al.
Current Protocols in Human Genetics|October 12, 2016
Molecular Diagnosis of Myotonic DystrophySujata Chakraborty, Matteo Vatta, Linda L Bachinski, et al.
Heartrhythm Case Reports|March 5, 2021
Maternal mosaicism in long QT syndrome due to a pathogenic variant in <i>KCNH2</i>Briana L Sawyer, Martin Tristani-Firouzi, Layne E Wells, et al.
Physiological Reports|November 22, 2021
Phosphorylation of Lamin A/C at serine 22 modulates Na<sub>v</sub> 1.5 functionMichael A Olaopa, Tomohiko Ai, Bo Chao, et al.
Frontiers in Cardiovascular Medicine|June 28, 2023
<i>De novo</i> heterozygous pathogenic <i>FBN1</i> variant in an autopsy case of multiple aneurysms and right renal artery dissection: a case reportTaylor MacGowan, Taylor McClinchey, Vibhu Parcha, et al.
American Journal of Medical Genetics. Part A|October 20, 2011
Coffin-Lowry syndrome and left ventricular noncompaction cardiomyopathy with a restrictive patternHugo R Martinez, Mary C Niu, V Reid Sutton, et al.
Pageof 13

Showing results (21-30 of 124) with videos related to

Sort By:
Pageof 13
European Heart Journal|February 17, 2007
Arrhythmogenic right ventricular cardiomyopathy: a 'final common pathway' that defines clinical phenotypeMatteo Vatta, Frank Marcus, Jeffrey A Towbin
Cardiology in the Young|April 16, 2005
Altered expression of dystrophin within the thoracic aorta in coarctationMatteo Vatta, Anthony C Chang, Colin J McMahon
Journal of Cardiovascular Medicine (Hagerstown, Md.)|February 6, 2009
Remodeling of dystrophin and sarcomeric Z-band occurs in pediatric cardiomyopathies: a unifying mechanism for force transmission defectMatteo Vatta, Gianfranco Sinagra, Luca Brunelli, et al.
Advances in Pediatrics|September 7, 2002
Genetics and cardiac arrhythmiasJeffrey A Towbin, Matteo Vatta, Hua Li, et al.
Circulation Research|February 17, 2007
Peroxisome proliferator-activated receptor-delta upregulates 14-3-3 epsilon in human endothelial cells via CCAAT/enhancer binding protein-betaLuca Brunelli, Katarzyna A Cieslik, Joseph L Alcorn, et al.
Current Protocols in Human Genetics|October 12, 2016
Molecular Diagnosis of Myotonic DystrophySujata Chakraborty, Matteo Vatta, Linda L Bachinski, et al.
Heartrhythm Case Reports|March 5, 2021
Maternal mosaicism in long QT syndrome due to a pathogenic variant in <i>KCNH2</i>Briana L Sawyer, Martin Tristani-Firouzi, Layne E Wells, et al.
Physiological Reports|November 22, 2021
Phosphorylation of Lamin A/C at serine 22 modulates Na<sub>v</sub> 1.5 functionMichael A Olaopa, Tomohiko Ai, Bo Chao, et al.
Frontiers in Cardiovascular Medicine|June 28, 2023
<i>De novo</i> heterozygous pathogenic <i>FBN1</i> variant in an autopsy case of multiple aneurysms and right renal artery dissection: a case reportTaylor MacGowan, Taylor McClinchey, Vibhu Parcha, et al.
American Journal of Medical Genetics. Part A|October 20, 2011
Coffin-Lowry syndrome and left ventricular noncompaction cardiomyopathy with a restrictive patternHugo R Martinez, Mary C Niu, V Reid Sutton, et al.
Pageof 13