Results 131 to 140 of about 65,798 (270)

Misdiagnoses of Hair and Scalp Disorders in Adult Patients With Skin of Color

International Journal of Dermatology, EarlyView.
Eric McMullen, Marissa Joseph, Samantha Mannala, Dea Metko, Shanti Mehta, Kristie Mar, Nawar Tarafdar, Kyobin Hwang, Touraj Khosravi‐Hafshejani, Mahan Maazi, Jeffrey Donovan   +10 more
wiley   +1 more source

Modulators of Diacylglycerol Kinase Activity: A Review of Advances and Challenges

Medicinal Research Reviews, Volume 46, Issue 1, Page 149-175, January 2026.
ABSTRACT Catalyzing the conversion of diacylglycerol (DAG) in phosphatidic acid (PA), diacylglycerol kinases (DGKs) play a pivotal role in all the physiological processes modulated by these two bioactive lipids, such as lipid metabolism and immune regulation.
Luisa Racca, Gianluca Baldanzi, Alberto Massarotti   +2 more
wiley   +1 more source

Tuberculosis-induced Autoimmune Hemolytic Anemia

Journal of the Indian Academy of Geriatrics
Autoimmune hemolytic anemia (AIHA) is a rare disorder characterized by antibodies against one’s own red blood cells, often difficult to diagnose and treat in the elderly. It can be secondary to an infection, drug, or a myeloproliferative disorder.
Shreya Biswal, Prasun Chatterjee
doaj   +1 more source

Genetic risk factors and clinical manifestations of systemic lupus erythematosus: Large‐scale analysis of genetic predisposition and disease subtypes

Journal of Internal Medicine, Volume 299, Issue 1, Page 95-108, January 2026.
Abstract Background Systemic lupus erythematosus (SLE) is an autoimmune disease with a heterogenous clinical picture. This study aimed to link genetic SLE predisposition with relevant clinical manifestations. Method Datasets best corresponding to the 11 American College of Rheumatology 1982 (ACR‐82) classification criteria for SLE in a large, public ...
Sarah Reid, Johanna K. Sandling, Pascal Pucholt, Ahmed Sayadi, Martina Frodlund, Karoline Lerang, Iva Gunnarsson, Andreas Jönsen, Ann‐Christine Syvänen, Øyvind Molberg, Solbritt Rantapää‐Dahlqvist, Anna Rudin, Christopher Sjöwall, Elisabet Svenungsson, Anders A. Bengtsson, Lars Rönnblom, Dag Leonard   +16 more
wiley   +1 more source

Thrombotic microangiopathies: thrombotic thrombocytopenic purpura / hemolytic uremic syndrome [PDF]

, 2010
Thrombotic microangiopathies (TMAs) are pathological conditions characterized by generalized microvascular occlusion by platelet thrombi, thrombocytopenia, and microangiopathic hemolytic anemia.
Mastroianni Kirsztajn, Gianna, Polito, Maria Goretti   +1 more
core   +2 more sources

Autologous Hematopoietic Stem Cell Transplantation in Systemic Sclerosis: Current Evidence and Future Directions

ACR Open Rheumatology, Volume 7, Issue 12, December 2025.
Systemic sclerosis (SSc) is a rare autoimmune connective tissue disease marked by progressive fibrosis and multi‐organ involvement, most notably in the lungs. Among patients with rapidly progressive diffuse cutaneous SSc and interstitial lung disease (ILD), autologous hematopoietic stem cell transplantation (AHSCT) has emerged as one of the most ...
Cristiana Sieiro Santos
wiley   +1 more source

Clinical and laboratory features of autoimmune hemolytic anemia associated with immune checkpoint inhibitors

American journal of hematology/oncology, 2019
Immune checkpoint inhibitors (ICPis) are a novel class of immunotherapeutic agents that have revolutionized the treatment of cancer; however, these drugs can also cause a unique spectrum of autoimmune toxicity.
R. K. Leaf, Christopher Ferreri, Deepa Rangachari, J. Mier, Wesley H Witteles, G. Ansstas, T. Anagnostou, L. Zubiri, Z. Piotrowska, T. Oo, D. Iberri, M. Yarchoan, A. Salama, Douglas B. Johnson, A. Leavitt, O. Rahma, K. Reynolds, D. Leaf   +17 more
semanticscholar   +1 more source

Pure Red Cell Aplasia Associated With Thymic Tumors, a Nationwide Retrospective Study

American Journal of Hematology, Volume 100, Issue 12, Page 2230-2237, December 2025.
ABSTRACT Pure red cell aplasia (PRCA) is the most frequent autoimmune cytopenia associated with thymic tumors (TTs). In a nationwide retrospective study, we included 41 patients (22 women, median age 62 years). At PRCA diagnosis, the mean hemoglobin level was 6.6 ± 2.1 g/dL, and the reticulocyte count was 6 ± 5 × 109/L. PRCA was diagnosed before TT (8%,
Mylène Hemmer, Sylvain Moinard, Olivier Lambotte, Marion Malphettes, Louis Terriou, Bertrand Lioger, Guillaume Le Guenno, Jean‐François Viallard, Marc Michel, Hervé Lobbes   +9 more
wiley   +1 more source

Ask a specialist : Ask a pathologist [PDF]

, 2014
Question: I ordered a type and screen on my patient, and the blood bank reported that her direct Coombs test was positive.
Coberly, Emily
core  

Eosinophilic fasciitis (Shulman's disease): review and comparative evaluation of seven patients. [PDF]

, 2019
OBJECTIVES: Eosinophilic fasciitis (EF) was described in 1974 by Shulman as a rare fibrosing connective tissue disease of unknown etiology. An undetermined trigger is thought to lead to the degranulation of eosinophils that interact with fibroblasts and
Cimbron, M, Farinha, F, Mendonça, T, Urzal, J   +3 more
core   +1 more source