Results 151 to 160 of about 21,508 (259)

Deciphering the full spectrum of Castleman diseases based on a cohort of 700 patients in a western country

British Journal of Haematology, Volume 208, Issue 6, Page 2036-2046, June 2026.
The spectrum of Castleman diseases has expanded over the past three decades. The phenotype of the diseases varies not only among the three major types but also according to the patient ancestry. Summary Under the Castleman disease (CD) eponym, three distinct diseases sharing common pathological features have been described over time.
Eric Oksenhendler, Marion Malphettes, Véronique Meignin, David Boutboul, Lionel Galicier   +4 more
wiley   +1 more source

Autoimmune Hemolytic Anemia Following Intravenous Immunoglobulin in Kawasaki Disease. [PDF]

Cureus
Pastrana Echevarria I, García J, Henriquez GM, Condor Y, Velazquez V.   +4 more
europepmc   +1 more source

Expanding Phenotype of GINS1 Deficiency: A Case Report and Review of the Literature

Clinical Genetics, Volume 109, Issue 6, Page 1076-1080, June 2026.
The authors present a novel case and review of individuals with GINS1 deficiency, causing severe growth restriction and combined immunodeficiency. Only the ninth case of this ultrarare disorder, it highlights the role of these variants in disease, glaucoma as a feature, and the possibility of immunodeficiency without infections in affected individuals.
Michael P. Mackley, Rae Brager, Hannah Geddie, Vicky Breakey, Rebecca Hough, Dimitrios J. Stavropoulos, Vanda McNiven   +6 more
wiley   +1 more source

Warm Autoimmune Hemolytic Anemia in an Elderly Patient With a History of Chronic Idiopathic Thrombocytopenic Purpura: A Case Report. [PDF]

Cureus
Pitaro AT, Bhat S, Ali MZ, Cavin A, Abraham RK.   +4 more
europepmc   +1 more source

Recurrent Mixed Autoimmune Hemolytic Anemia With Evans Syndrome and High-Risk Relapse Features: A Case Report. [PDF]

Cureus
Nguyen KT, Win KHH, Huynh D, Rambhia H, Panigrahi K, Kalavar MR, Guillaume E.   +6 more
europepmc   +1 more source

A case of autoimmune hemolytic anemia with acquired functional mutation of the TLR7. [PDF]

Immunol Res
Han Y, Chen H, Li Y, Yin Y, Zhu X, Wu X.
europepmc   +1 more source

Autoimmune Hemolytic Anemia in Children

Yonsei Medical Journal, 1987
D C, Park, C H, Yang, K Y, Kim
openaire   +2 more sources

Autoimmune hemolytic anemia in visceral leishmaniasis

, 1999
A case of an 8-month old male child, who presented with lgG mediated Coomb’s positive hemolytic anemia and visceral leishmaniasis is presented. The hemolytic anemia resolved following the treatment of leishmaniasis.
Adil, Salman, Khurshid, Mohammad, Burney, lkram A.   +2 more
core  

Relative Exchangeable and Exchangeable Copper: Emerging New Biomarkers for Diagnosis and Therapy Monitoring in Wilson's Disease

Liver International, Volume 46, Issue 6, June 2026.
ABSTRACT Background and Aims Wilson's disease (WD) is a genetic disorder of copper metabolism in which early diagnosis remains challenging, particularly in acute liver failure (ALF). Relative exchangeable copper (REC) and exchangeable copper (CuEXC) are emerging biomarkers for diagnosis and monitoring, but data from larger cohorts are limited.
Sebastian Köhrer, Antoan Rusev, Holger Zimmer, Silke Wolf, Jessica Langel, Andrea Langel, Thomas Longerich, Patrick Michl, Moritz Niesert, Alexander Fichtner, Isabelle Mohr   +10 more
wiley   +1 more source

Cold Agglutinin-Mediated Hemolytic Anemia Preceding the Diagnosis of Acute Myeloid Leukemia: A Case Report and Literature Review. [PDF]

Cureus
Tariq MA, Almahmood M, Mushtaq J, Incorvati J.   +3 more
europepmc   +1 more source