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Matteo Vatta

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Journal of Neuromuscular Diseases|June 10, 2025

Clinical validity of congenital myopathy genes determined by the ClinGen Congenital Myopathies Expert PanelJustyne E Ross, May Flowers, Shannon McNulty, et al.

Circulation|January 30, 2015

Dysfunction in the βII spectrin-dependent cytoskeleton underlies human arrhythmiaSakima A Smith, Amy C Sturm, Jerry Curran, et al.

JAMA|August 1, 2023

Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European AncestryElizabeth Jordan, Daniel D Kinnamon, Garrie J Haas, et al.

European Heart Journal|June 7, 2019

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, David J Tester, et al.

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Search research articles

Showing results (121-130 of 124) with videos related to

Sort By:

Pageof 13

You have reached the last page of results.This site can display upto 124 results.

Journal of Neuromuscular Diseases|June 10, 2025

Clinical validity of congenital myopathy genes determined by the ClinGen Congenital Myopathies Expert PanelJustyne E Ross, May Flowers, Shannon McNulty, et al.

Circulation|January 30, 2015

Dysfunction in the βII spectrin-dependent cytoskeleton underlies human arrhythmiaSakima A Smith, Amy C Sturm, Jerry Curran, et al.

JAMA|August 1, 2023

Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European AncestryElizabeth Jordan, Daniel D Kinnamon, Garrie J Haas, et al.

European Heart Journal|June 7, 2019

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, David J Tester, et al.

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