Results 131 to 140 of about 34,385 (232)

SGLT‐2 inhibitors for cardiac amyloidosis: Hype or hope?

European Journal of Clinical Investigation, Volume 55, Issue 11, November 2025.
Flavio Tangianu, Eleonora Nicolini, Francesco Dentali, Aldo Bonaventura   +3 more
wiley   +1 more source

A patient with AL amyloidosis presenting with refractory tuberculosis, chest tightness and hypotension: case report

BMC Pulmonary Medicine
Introduction Immunoglobulin light chain (AL) amyloidosis presents a clinical spectrum characterized by diverse manifestations and involvement of multiple organs, posing a significant diagnostic challenge for physicians.
Jun Yang, Mohamed Fahim Fathima Farhath, Huohuan Tian, Linhui Yang, Dan Liu   +4 more
doaj   +1 more source

Primary systemic amyloidosis presenting as macroglossia

Saudi Journal of Oral Sciences, 2017
Primary amyloidosis is a group of monoclonal plasma cell disorders, characterized by extracellular deposition of immunoglobulin light chain fibrils in multiple organs leading to progressive multiorgan dysfunction.
Anamika Aluri, Majed Momin, Abhijeet Ingle, G Vamshi Krishna Reddy, Karishma Rosann Pereira   +4 more
doaj   +1 more source

Relationship between aetiology and left ventricular systolic dysfunction in hypertrophic cardiomyopathy. [PDF]

, 2017
BACKGROUND: Severe left ventricular (LV) systolic dysfunction is an uncommon complication of hypertrophic cardiomyopathy (HCM) that is associated with poor prognosis.
Biagini, Biagini, Biagini, Biagini, Chan, Child, Dubrey, Elliott, Elliott, Gersh, Giunta, Harris, Lopes, Maron, Maron, McKenna, Ng, O'Mahony, Rapezzi, Rapezzi, Shah, Spirito, Thaman   +22 more
core   +2 more sources

Expert Perspective: Hematologic Malignancies and Vasculitis

Arthritis &Rheumatology, Volume 77, Issue 10, Page 1305-1316, October 2025.
Michelle L. Robinette, Hetty E. Carraway
wiley   +1 more source

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

Gastric Amyloidosis [PDF]

, 2006
Amyloidosis occurs as secondary to rheumatoid arthritis, inflammatory bowel disease and other diseases and also associated with familial Mediterranean fever. Outcomes are worse if there are cardiac or gastrointestinal manifestations. A 57 year-old female
Fauzi, A. (Achmad), Raditya, F. (Fajar), Rani, A. A. (Abdul), Syam, A. F. (Ari)   +3 more
core  

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

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

Stronger inflammatory/cytotoxic T cell response in women identified by microarray analysis [PDF]

, 2008
Women develop chronic inflammatory autoimmune diseases like lupus more often than men. The mechanisms causing the increased susceptibility are incompletely understood, although estrogen is believed to contribute.
Anura Hewagama, Bruce C. Richardson, Dipak Patel, Faith M. Strickland, Sushma Yarlagadda   +4 more
core   +1 more source