Articles with "cardiac pathology" as a keyword



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Cardiac Remodeling and Disease: SOCE and TRPC Signaling in Cardiac Pathology.

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Published in 2017 at "Advances in experimental medicine and biology"

DOI: 10.1007/978-3-319-57732-6_25

Abstract: TRPC channels have been suggested as potential candidates mediating store-operated Ca2+ entry (SOCE) in cardiomyocytes. There is increasing evidence that the TRPC isoforms TRPC1 and TRPC4 might fulfill the function as SOCs, in concert with… read more here.

Keywords: trpc channels; disease; trpc; pathology ... See more keywords
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Cardiac pathology 6 months after hospitalization for COVID-19 and association with the acute disease severity

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Published in 2021 at "American Heart Journal"

DOI: 10.1016/j.ahj.2021.08.001

Abstract: Background COVID-19 may cause myocardial injury and myocarditis, and reports of persistent cardiac pathology after COVID-19 have raised concerns of long-term cardiac consequences. We aimed to assess the presence of abnormal cardiovascular resonance imaging (CMR)… read more here.

Keywords: hospitalization; disease; pathology; association ... See more keywords
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Evolution of cardiac pathology in classic Fabry disease: Progressive cardiomyocyte enlargement leads to increased cell death and fibrosis, and correlates with severity of ventricular hypertrophy‬‬‬‬‬‬‬‬.

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Published in 2017 at "International journal of cardiology"

DOI: 10.1016/j.ijcard.2017.06.079

Abstract: BACKGROUND Fabry disease, an X-linked lysosomal storage disease, results from deficient α-galactosidase A (α-GalA) activity and the systemic accumulation of α-galactosyl-terminated glycosphingolipids. Two major phenotypes, "Classic" and "Later-Onset", lead to renal failure, and/or cardiac disease,… read more here.

Keywords: disease; pathology; hypertrophy; cardiac pathology ... See more keywords
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Cardiac pathology in spinal muscular atrophy: a systematic review

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Published in 2017 at "Orphanet Journal of Rare Diseases"

DOI: 10.1186/s13023-017-0613-5

Abstract: BackgroundHereditary proximal spinal muscular atrophy (SMA) is a severe neuromuscular disease of childhood caused by homozygous loss of function of the survival motor neuron (SMN) 1 gene. The presence of a second, nearly identical SMN… read more here.

Keywords: spinal muscular; pathology; patients sma; muscular atrophy ... See more keywords