Andrew Chisom Madu il 30/05/2026

More Than Myocarditis? Cardiac Involvement in Phaeochromocytoma-A Case Report

Br J Hosp Med (Lond). 2026 May 18;87(5):53981. doi: 10.31083/BJHM53981.ABSTRACTAIMS/BACKGROUND: Phaeochromocytoma is a rare catecholamine-secreting neuroendocrine tumour arising from chromaffin cells of the adrenal medulla or from extra-adrenal paraganglionic tissue, in which case it is termed parag

Le He il 28/05/2026

ATF5 reduces LPS-induced cardiac injury by modulating pyroptosis via mitophagy

J Bioenerg Biomembr. 2026 May 8;58(1):12. doi: 10.1007/s10863-026-10102-4.ABSTRACTMyocarditis, often triggered by infections such as sepsis, involves complex mechanisms including mitochondrial dysfunction, oxidative stress and inflammation. The role of activating transcription factor 5 (ATF5) in myo

Jingyi Long il 28/05/2026

Efficacy and safety of Songjiao Dihuang Tang decoction for the dynamic/adaptive treatment of immune checkpoint inhibitor-associated myocarditis: study protocol and statistical analysis plan for a stop&go, multicentre, randomized, parallel-controlled, double-blind, superiority clinical trial

Front Pharmacol. 2026 May 12;17:1797368. doi: 10.3389/fphar.2026.1797368. eCollection 2026.ABSTRACTBACKGROUND: While immune checkpoint inhibitors (ICIs) enhance tumour therapy, immune checkpoint inhibitor-associated myocarditis (ICIAM) pose risks of mortality because of their low incidence and rapid

Paul Ehiabhi Ikhurionan il 27/05/2026

Diphtheritic polyneuropathy: Not so uncommon

Trop Doct. 2026 May 27:494755261454023. doi: 10.1177/00494755261454023. Online ahead of print.ABSTRACTDiphtheria is a potentially fatal infection owing to its life-threatening complications of respiratory obstruction and myocarditis. Less often reported is diphtheritic polyneuropathy (DP), which ref

Odile Boespflug-Tanguy il 27/05/2026

Death following high-dose AAV9 gene therapy in a patient with advanced SMA-PME

Mol Ther. 2026 May 26:S1525-0016(26)00403-X. doi: 10.1016/j.ymthe.2026.05.016. Online ahead of print.ABSTRACTSpinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME) is an ultra-rare, fatal autosomal recessive disorder caused by ASAH1 mutations, with no curative treatment. We report the

Gallage H D N Ariyaratne il 27/05/2026

A Paradigm Shift: Arrhythmogenic Cardiomyopathy Is an Inflammatory Disease

Cells. 2026 May 9;15(10):868. doi: 10.3390/cells15100868.ABSTRACTArrhythmogenic cardiomyopathy (ACM) is a genetic myocardial disorder marked by progressive cardiomyocyte loss, fibro-fatty replacement, ventricular arrhythmias, and risk of sudden cardiac death. Traditionally considered a structural an