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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
A patient with AL amyloidosis presenting with refractory tuberculosis, chest tightness and hypotension: case report. [PDF]
Yang J+4 more
europepmc +1 more source
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]
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]
Brunger AF+12 more
europepmc +1 more source
A Simple Frailty Score Predicts Survival and Early Mortality in Systemic AL Amyloidosis. [PDF]
Ríos-Tamayo R+18 more
europepmc +1 more source
Correction to "Risk factors for severe infection and mortality in patients with COVID-19 in patients with multiple myeloma and AL amyloidosis". [PDF]
europepmc +1 more source
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Immunotherapy in AL Amyloidosis
Current Treatment Options in Oncology, 2022Light-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
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Once AL amyloidosis: not always AL amyloidosis
Amyloid, 2018Amyloid cardiomyopathy could be related to AL amyloidosis, wild-type transthyretin amyloidosis (ATTRwt) or hereditary amyloidosis (ATTRm).
Tulip Jhaveri+5 more
openaire +3 more sources