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Health
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Heart Disease
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My 19th Heart Valve Surgery Anniversary!
Heart Disease
webtechlake
-
December 19, 2024
Written By: Adam Pick, Patient Advocate, Author & Website FounderPublished: December 19, 2024It’s hard to believe.This coming Saturday, December 21, I will celebrate my...
Journal club debates : Can “Aim of a study” be wrong ?
Heart Disease
webtechlake
-
December 18, 2024
Journal club debates : Can “Aim of a study” be wrong ? December 18, 2024 by dr s venkatesan Absolutely yes. The number...
“One + one” is rarely two in biology. The wronged mathematics of high risk pregnancy
Heart Disease
webtechlake
-
December 18, 2024
“One + one” is rarely two in biology. The wronged mathematics of high risk pregnancy December 18, 2024 by dr...
Steve’s Warning for Heart Surgery Patients
Heart Disease
webtechlake
-
December 17, 2024
Written By: Adam Pick, Patient Advocate, Author & Website FounderPublished: December 17, 2024As we have seen many times in...
Optimising management of moderate secondary mitral regurgitation: insights into pharmacological and interventional approaches
Heart Disease
webtechlake
-
December 16, 2024
Secondary mitral regurgitation (SMR) is a complex and evolving challenge in the landscape of heart failure (HF) management....
Correction: The efficacy of extraembryonic stem cells in improving blood flow within animal models of lower limb ischaemia
Heart Disease
webtechlake
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December 15, 2024
Mohamed Omer S, Krishna SM, Li J, et al. The efficacy of extraembryonic stem cells in improving blood...
Diagnostic accuracy of non-invasive cardiac imaging modalities in patients with a history of coronary artery disease: a meta-analysis
Heart Disease
webtechlake
-
December 15, 2024
WHAT IS ALREADY KNOWN ON THIS TOPICThe diagnostic performance of various non-invasive imaging techniques for detecting coronary artery...
Effects of resveratrol on aortic growth in patients with Marfan syndrome: a single-arm open-label multicentre trial
Heart Disease
webtechlake
-
December 15, 2024
IntroductionMarfan syndrome (MFS) is an inherited connective tissue disorder caused almost exclusively by mutations in the fibrillin-1 (FBN1)...
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