Results 261 to 270 of about 37,267 (288)

Impact of Elevated Preprocedural Left Ventricular Filling Pressure on Prognosis of Mild Paravalvular Regurgitation Following Transcatheter Aortic Valve Replacement

open access: yesCatheterization and Cardiovascular Interventions, Volume 106, Issue 1, Page 242-249, July 1, 2025.
ABSTRACT Background Paravalvular regurgitation (PVR) following transcatheter aortic valve replacement (TAVR) is a complication linked to poor outcomes. The prognostic impact of mild PVR, particularly in patients with elevated preprocedural left ventricular (LV) filling pressure, remains uncertain.
Shumpei Kosugi   +12 more
wiley   +1 more source

The Herald Bleed—A Fortunate Endoscopic Diagnosis of an Aorto‐Duodenal Fistula Secondary to a Mycotic Aortic Aneurysm With Abscess Formation

open access: yesClinical Case Reports, Volume 13, Issue 7, July 2025.
ABSTRACT Aorto‐duodenal fistula is a rare but catastrophic cause of gastrointestinal bleeding. A high index of suspicion is required for diagnosis. Reviewing previous imaging provides essential hints. A pulsatile clot or bleeding source can be seen on endoscopy. Management is surgical with multi‐disciplinary involvement.
Arteen Arzivian   +2 more
wiley   +1 more source

Helical superstructures between amyloid and collagen in cardiac fibrils from a patient with AL amyloidosis. [PDF]

open access: yesNat Commun
Schulte T   +20 more
europepmc   +1 more source

Diagnostic performance of liver stiffness as marker of liver involvement in systemic immunoglobulin light chain (AL) amyloidosis. [PDF]

open access: yesAnn Hematol
Brunger AF   +12 more
europepmc   +1 more source

A Simple Frailty Score Predicts Survival and Early Mortality in Systemic AL Amyloidosis. [PDF]

open access: yesCancers (Basel)
Ríos-Tamayo R   +18 more
europepmc   +1 more source

Immunotherapy in AL Amyloidosis

Current Treatment Options in Oncology, 2022
Light-chain amyloidosis is a rare disorder where a small clone of plasma cells is producing excess toxic light chains that deposit in various organs and cause dysfunction. Cardiac involvement is a major determinant of survival and rapid reduction of light chain is critical for recovery of organ function and overall survival. Immunotherapy targeting the
Yifei, Zhang, Raymond L, Comenzo
openaire   +2 more sources

Once AL amyloidosis: not always AL amyloidosis

Amyloid, 2018
Amyloid cardiomyopathy could be related to AL amyloidosis, wild-type transthyretin amyloidosis (ATTRwt) or hereditary amyloidosis (ATTRm).
Tulip Jhaveri   +5 more
openaire   +3 more sources

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