Results 101 to 110 of about 8,373 (204)

Cardiac amyloidosis

Annales Academiae Medicae Silesiensis
Amyloidosis is a rare disease characterized by an abnormal accumulation of the amyloid protein in tissues. Amyloidosis can be divided into two main subtypes: transthyretin amyloidosis (ATTR-CA) and immunoglobulin light chain amyloidosis (AL-CA ...
Magdalena Balwierz, Bartosz Gruchlik, Katarzyna Mizia-Stec   +2 more
doaj   +1 more source

Refractory IgM AL amyloidosis with massive soft tissue tumors: Rescue with zanubrutinib. A case report

Current Problems in Cancer: Case Reports
Waldenström macroglobulinemia (WM) is a rare indolent B-cell non-Hodgkin lymphoma with lymphoplasmacytic morphology, associated with immunoglobulin M (IgM) monoclonal gammopathy. The coexistence of WM and immunoglobulin light chain (AL) amyloidosis is an
Piotr Jachimowski, Łukasz Ciulkiewicz, Mateusz Ziarkiewicz, Bogna Ziarkiewicz-Wróblewska, Marta Legatowicz-Koprowska, Krzysztof Jamroziak   +5 more
doaj   +1 more source

Safety and efficacy of teclistamab in systemic immunoglobulin light chain amyloidosis. [PDF]

Blood Cancer J, 2023
Chakraborty R, Bhutani D, Maurer MS, Mohan M, Lentzsch S, D'Souza A.   +5 more
europepmc   +1 more source

A risk stratification for systemic immunoglobulin light‐chain amyloidosis with renal involvement [PDF]

, 2019
Ting Li, Xianghua Huang, Qingwen Wang, Liang Zhao, Guisheng Ren, Wencui Chen, Pengfei Zheng, Minlin Zhou, Qi Jiang, Ru Yin, Zhihong Liu   +10 more
openalex   +1 more source

Immunoglobulin light chain amyloidosis involved multiple organs [PDF]

QJM: An International Journal of Medicine, 2019
J, Bai, J, Qiao, H, Fang
openaire   +2 more sources

Syndrome in question. Immunoglobulin light chain amyloidosis.

Anais brasileiros de dermatologia, 2015
Immunoglobulin light chain amyloidosis is the most common acquired systemic amyloidosis. Its presentation is often insidious and progressive, which may delay diagnosis. The authors describe a rare case of immunoglobulin light chain amyloidosis in a 34-year-old man with scleroderma-like manifestation substantiated by multifarious laboratory ...
Han, Ma, Meilan, Chen, Juan, Li, Ying, Li, Shu, Qiu   +4 more
openaire   +1 more source

Immunoglobulin light chain amyloidosis: 2018 Update on diagnosis, prognosis, and treatment [PDF]

, 2018
Morie A. Gertz
openalex   +1 more source

Alterations of the gut microbiota in patients with immunoglobulin light chain amyloidosis. [PDF]

Front Immunol, 2022
Yan J, Zhao J, Ning X, Qin Y, Xing Y, Wang Y, Jia Q, Huang B, Ma R, Lei C, Zhou M, Yu Z, Zhang Y, Guo WF, Sun S.   +14 more
europepmc   +1 more source

How We Manage Systemic Immunoglobulin Heavy Chain Amyloidosis (AH Amyloidosis) and Immunoglobulin Heavy-and-Light-Chain Amyloidosis (AH/AL Amyloidosis) [PDF]

Clinical Lymphoma Myeloma and Leukemia, 2020
Chakra P. Chaulagain, Leal C. Herlitz, Julie Fu, Nadeem Bilani, Camerun Lucitt, Raymond L. Comenzo   +5 more
openaire   +2 more sources

Role of implantable intracardiac defibrillators in patients with cardiac immunoglobulin light chain amyloidosis [PDF]

, 2017
Tamer Rezk, Carol Whelan, Helen J. Lachmann, Marianna Fontana, Sajitha Sachchithanantham, Shameem Mahmood, Fakhar Z. Khan, Raj Khiani, Joseph Tomson, Taryn Youngstein, Julian D. Gillmore, Philip N. Hawkins, Ashutosh Wechalekar   +12 more
openalex   +1 more source