Results 251 to 260 of about 607,470 (403)
Abstract Wild‐type transthyretin amyloid cardiomyopathy (ATTRwt‐CM) is a progressive and infiltrative cardiac disorder that may cause fatal consequences if left untreated. The estimated survival time from diagnosis is approximately 3–6 years. Because of the non‐specificity of initial symptom manifestation and insufficient awareness among treating ...
Yasuhiro Izumiya+9 more
wiley +1 more source
Obstructive Hypertrophic Cardiomyopathy and Aortic Stenosis With High Surgical Risk
Background: Treatment and accurate assessment of aortic valve stenosis (AS) with concomitant obstructive hypertrophic cardiomyopathy (HCM) prove challenging.
Omar M. Abdelfattah, MD+3 more
doaj
Electrophysiological properties of right heart and atrioventricular conducting system in patients with alcoholic cardiomyopathy. [PDF]
C Luca
openalex +1 more source
Abstract Sodium‐glucose co‐transporters (SGLTs) mediate sodium and glucose transport across cell membranes. SGLT2 inhibitors have a recognized place within heart failure (HF) guidelines. We evaluated the effect of sotagliflozin on HF and cardiovascular outcomes in participants with type 2 diabetes. Scopus, Medline, Embase and Central were searched from
Maria Anna Bantounou+7 more
wiley +1 more source
Vincent Y. See, Libin Wang
doaj +1 more source
Incidence of positive genetic testing among patients referred for cardiac positron emission tomography. [PDF]
Trinh K, Dries A, Boulier K, Wang J.
europepmc +1 more source
Histochemical, ultrastructural and structural changes in primary cardiomyopathy and in cobalt cardiomyopathy [PDF]
E. G. J. Olsen
openalex +1 more source
Abstract Aims The prognostic role of high‐sensitivity cardiac troponin T (hs‐cTnT) as a biomarker in patients with cardiac sarcoidosis (CS) has yet to be fully determined, especially when compared with B‐type natriuretic peptide (BNP). Methods and Results In this post‐hoc analysis of the ILLUMINATE‐CS (ILLUstration of the Management and prognosIs of ...
Yuichi Baba+10 more
wiley +1 more source
Early-onset restrictive cardiomyopathy with life-threatening arrhythmia caused by a homozygous desmin mutation: a case report. [PDF]
Wang T+6 more
europepmc +1 more source