Results 131 to 140 of about 37,267 (288)
Sex differences in heart failure (HF) management and outcomes in the French‐DataHF cohort. CI, confidence interval; HFH, heart failure hospitalization; HR, hazard ratio; IPW, inverse probability weighting; KM, Kaplan–Meier; LD, loop diuretic; RAS, renin–angiotensin system; RASi, renin–angiotensin system inhibitor.
Guillaume Baudry+7 more
wiley +1 more source
Ascites revealing peritoneal amyloidosis and IgG kappa multiple myeloma: A case report
AL amyloidosis is a rare systemic disease characterized by the deposition of amyloid protein in various organs, including the kidneys, heart, peripheral nervous system, digestive tract, skin, and muscles.
Samia Sabri+4 more
doaj
Unusual manifestation of AL amyloidosis—stenosis of inferior vena cava [PDF]
Zuzana Říhová+10 more
openalex +1 more source
Exploring the Potential and Advancements of Circular RNA Therapeutics
Given the remarkable advantages in terms of stability, sustained expression profile, safety, wide range of druggable targets, scalable and cost‐effective manufacturing capabilities, circRNA is currently undergoing intensive investigation for various therapeutic applications such as vaccines, protein replacement, genetic disease treatment, gene therapy,
Lei Wang+6 more
wiley +1 more source
A retrospective analysis of the impact of erythropoeitic growth factor utilization on transfusion requirements in patients with AL amyloidosis undergoing autologous SCT [PDF]
David Baribeault+5 more
openalex +1 more source
A Long-Survival Case of Systemic AL Amyloidosis with Nephrotic Syndrome.
Tomoko Katagiri+5 more
openalex +2 more sources
Localized primary AL-type amyloidosis of the jejunum diagnosed by double-balloon enteroscopy [PDF]
Michael Bellutti+6 more
openalex +1 more source
Abstract Purpose To develop a cardiac MR fingerprinting (cMRF) approach using deep image prior reconstruction (DIP) to simultaneously map T1, T2, and T1ρ, and assess T1ρ in healthy subjects and patients with areas of enhancement on late gadolinium enhancement.
Sydney Kaplan+6 more
wiley +1 more source
ABSTRACT Introduction/Aims Hereditary transthyretin amyloidosis (ATTRv) is an autosomal dominant multisystem disorder that occurs worldwide. The most common mutation in the United States, V142I, has previously been described as having a primarily cardiac presentation.
Urvi Desai+3 more
wiley +1 more source