Results 191 to 200 of about 4,786,755 (237)

The Association of Kidney Function on Survival in Patients with Amyloid Light Chain Amyloidosis after Autologous Stem Cell Transplantation: A Multicenter Study. [PDF]

open access: yesKidney360
Selamet U   +12 more
europepmc   +1 more source

Renal heavy and light chain amyloidosis: A rare case report. [PDF]

open access: yesMedicine (Baltimore)
Chen B   +5 more
europepmc   +1 more source

Immunoglobulin light chain amyloidosis

open access: yesExpert Review of Hematology, 2013
Primary light chain amyloidosis is the most common form of systemic amyloidosis and is caused by misfolded light chains that cause proteotoxicity and rapid decline of vital organ function. Early diagnosis is essential in order to deliver effective therapy and prevent irreversible organ damage.
MERLINI, GIAMPAOLO   +4 more
openaire   +4 more sources

Amyloidosis and Light Chain Plasmocytoma

open access: yesTumori Journal, 1976
Nine cases of light chain plasmocytomas, 6 type λ and 3 type k, have been studied in reference to amyloid presence and localisation. Bone marrow plasmocytosis, light chains in serum and/or in the urine, and osteolytic lesions were demonstrated in all the patients.
G, Tosato, E, Fagiolo
openaire   +3 more sources

Advances in the treatment of light chain amyloidosis

Current Opinion in Oncology, 2022
Purpose of review After many years, the management of systemic light chain (AL) amyloidosis is entering the era of evidence-based medicine, with three recently published randomized clinical trials, a regimen (daratumumab, cyclophosphamide, bortezomib, and dexamethasone, daratumumab-CyBorD) labeled for upfront therapy, more ...
Palladini, Giovanni, Milani, Paolo
openaire   +3 more sources

Coagulation Abnormalities in Light Chain Amyloidosis

Mayo Clinic Proceedings, 2021
To assess the prevalence of coagulation abnormalities in patients with systemic light chain (AL) amyloidosis and their association with disease-related characteristics, disease progression, and survival.This is a retrospective study of patients with AL amyloidosis seen at Mayo Clinic, Rochester, Minnesota, from January 1, 2006, to December 31, 2015. We
Nadine Abdallah   +16 more
openaire   +2 more sources

Light-chain cardiac amyloidosis

Current Problems in Cancer, 2017
Cardiac amyloidosis is an underrecognized condition, in which delays to diagnosis have great implications on management options, prognosis, and morbidity. Once cardiac tissue is infiltrated by amyloid fibrils, there is a cascade of pathologic changes that can display an array of clinical manifestations, from impaired relaxation of the ventricular ...
Anit K, Mankad   +2 more
openaire   +2 more sources

Macroglossia in Light-Chain Amyloidosis

New England Journal of Medicine, 2018
Macroglossia in Light-Chain Amyloidosis A 78-year-old man presented with enlargement and stiffening of the tongue. Biopsy confirmed that this finding of macroglossia was due to light-chain amyloidosis.
João Melo Alves, Natália Marto
openaire   +2 more sources

[Light chain amyloidosis].

Innere Medizin (Heidelberg, Germany), 2023
Light chain amyloidosis (AL) is a rare protein deposition disease. It is caused by a clonal plasma cell or B‑cell disease in the bone marrow. With the exception of the central nervous system, all organs can be affected by amyloid deposits. Cardiac involvement is the most frequent organ manifestation that leads to significantly increased mortality when ...
Ute, Hegenbart   +2 more
openaire   +1 more source

Home - About - Disclaimer - Privacy