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Matteo Vatta

Showing results (61-70 of 124) with videos related to

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Lancet (London, England)|March 29, 2002
Molecular remodelling of dystrophin in patients with end-stage cardiomyopathies and reversal in patients on assistance-device therapyMatteo Vatta, Sonny J Stetson, Alejandro Perez-Verdia, et al.
Plos One|March 21, 2014
ZASP interacts with the mechanosensing protein Ankrd2 and p53 in the signalling network of striated muscleValentina C Martinelli, W Buck Kyle, Snezana Kojic, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 23, 2024
Clinical utility of polygenic risk scores for embryo selection: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)Theresa A Grebe, George Khushf, John M Greally, et al.
Journal of Cardiovascular Electrophysiology|March 3, 2007
A common SCN5A variant alters the responsiveness of human sodium channels to class I antiarrhythmic agentsMossaab Shuraih, Tomohiko Ai, Matteo Vatta, et al.
Molecular Genetics & Genomic Medicine|September 7, 2019
A novel TTN deletion in a family with skeletal myopathy, facial weakness, and dilated cardiomyopathyJennifer Roggenbuck, Kelly Rich, Ana Morales, et al.
Human Genetics|February 22, 2003
Assessment of the CTNNA3 gene encoding human alpha T-catenin regarding its involvement in dilated cardiomyopathyBarbara Janssens, Bhagyalaxmi Mohapatra, Matteo Vatta, et al.
Heart Rhythm|August 4, 2009
A novel SCN5A mutation V1340I in Brugada syndrome augmenting arrhythmias during febrile illnessKaveh Samani, Geru Wu, Tomohiko Ai, et al.
Cardiogenetics|December 10, 2013
LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotypeJianding Cheng, David W Van Norstrand, Argelia Medeiros-Domingo, et al.
Heart Rhythm|May 12, 2016
Arrhythmogenic calmodulin mutations impede activation of small-conductance calcium-activated potassium currentChih-Chieh Yu, Jum-Suk Ko, Tomohiko Ai, et al.
JAMA Neurology|May 24, 2013
Clinical application of whole-exome sequencing: a novel autosomal recessive spastic ataxia of Charlevoix-Saguenay sequence variation in a child with ataxiaWendy K M Liew, Tawfeg Ben-Omran, Basil T Darras, et al.
Pageof 13

Showing results (61-70 of 124) with videos related to

Sort By:
Pageof 13
Lancet (London, England)|March 29, 2002
Molecular remodelling of dystrophin in patients with end-stage cardiomyopathies and reversal in patients on assistance-device therapyMatteo Vatta, Sonny J Stetson, Alejandro Perez-Verdia, et al.
Plos One|March 21, 2014
ZASP interacts with the mechanosensing protein Ankrd2 and p53 in the signalling network of striated muscleValentina C Martinelli, W Buck Kyle, Snezana Kojic, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 23, 2024
Clinical utility of polygenic risk scores for embryo selection: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)Theresa A Grebe, George Khushf, John M Greally, et al.
Journal of Cardiovascular Electrophysiology|March 3, 2007
A common SCN5A variant alters the responsiveness of human sodium channels to class I antiarrhythmic agentsMossaab Shuraih, Tomohiko Ai, Matteo Vatta, et al.
Molecular Genetics & Genomic Medicine|September 7, 2019
A novel TTN deletion in a family with skeletal myopathy, facial weakness, and dilated cardiomyopathyJennifer Roggenbuck, Kelly Rich, Ana Morales, et al.
Human Genetics|February 22, 2003
Assessment of the CTNNA3 gene encoding human alpha T-catenin regarding its involvement in dilated cardiomyopathyBarbara Janssens, Bhagyalaxmi Mohapatra, Matteo Vatta, et al.
Heart Rhythm|August 4, 2009
A novel SCN5A mutation V1340I in Brugada syndrome augmenting arrhythmias during febrile illnessKaveh Samani, Geru Wu, Tomohiko Ai, et al.
Cardiogenetics|December 10, 2013
LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotypeJianding Cheng, David W Van Norstrand, Argelia Medeiros-Domingo, et al.
Heart Rhythm|May 12, 2016
Arrhythmogenic calmodulin mutations impede activation of small-conductance calcium-activated potassium currentChih-Chieh Yu, Jum-Suk Ko, Tomohiko Ai, et al.
JAMA Neurology|May 24, 2013
Clinical application of whole-exome sequencing: a novel autosomal recessive spastic ataxia of Charlevoix-Saguenay sequence variation in a child with ataxiaWendy K M Liew, Tawfeg Ben-Omran, Basil T Darras, et al.
Pageof 13