Results 111 to 120 of about 13,305 (193)

Potential Contribution of <i>DES</i> (p.Leu88Met) and <i>MYH7</i> (p.Arg787His) Variants to Familial Restrictive Cardiomyopathy. [PDF]

open access: yesCardiol Res Pract
Bagherimoghaddam M   +8 more
europepmc   +1 more source

Autopsy of a patient with restrictive cardiomyopathy with and MYH7 mutation

open access: yesAutopsy of a patient with restrictive cardiomyopathy with and MYH7 mutation
Restrictive cardiomyopathy (RCM) is a rare type of primary myocardial disease, and its pathological features remain unclear. We report the case of a 78-year-old Japanese woman with RCM and MHY7 mutation who died of heart failure 13 years after the diagnosis. Upon autopsy, focal myocyte amorphous degeneration positive for ubiquitin was revealed, as well
openaire   +1 more source

Different substitutions at the same β-myosin residue underlie divergent molecular phenotypes and distinct cardiomyopathies. [PDF]

open access: yesJ Biol Chem
Lehman SJ   +9 more
europepmc   +1 more source

Heart-reactive antibody levels differentially associate with ventricular function in hereditary cardiomyopathies. [PDF]

open access: yesBMC Cardiovasc Disord
Schiffer D   +14 more
europepmc   +1 more source

Identifying Cardiac Autoantibody Biomarkers that Predict the Severity of Chagas Cardiomyopathy. [PDF]

open access: yesJACC Basic Transl Sci
Ribeiro H   +26 more
europepmc   +1 more source

Genotype-Dependent Effects of Mechanical Stretch and GATA4-Targeted Compound 3i-1262 in Cardiomyopathy Patient-Derived hiPSC-Cardiomyocytes. [PDF]

open access: yesBasic Clin Pharmacol Toxicol
Pohjavaara S   +5 more
europepmc   +1 more source

Thick filament molecular interfaces play a critical role in the pathogenesis of hypertrophic cardiomyopathy. [PDF]

open access: yesProc Natl Acad Sci U S A
Dutta D   +6 more
europepmc   +1 more source

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