Results 71 to 80 of about 65,798 (270)

Positive predictive value of diagnosis coding for hemolytic anemias in the Danish National Patient Register [PDF]

, 2016
PURPOSE: The nationwide public health registers in Denmark provide a unique opportunity for evaluation of disease-associated morbidity if the positive predictive values (PPVs) of the primary diagnosis are known.
Frederiksen, Henrik, Hansen, Dennis Lund, Overgaard, Ulrik Malthe, Pedersen, Lars   +3 more
core   +2 more sources

Tegsedi-Induced Warm Antibody Autoimmune Hemolytic Anemia

Annals of Internal Medicine: Clinical Cases
Autoimmune hemolytic anemia is a hemolytic disorder in which antibodies attack erythrocytes, causing their destruction. Many medications have been linked to autoimmune hemolytic anemia, such as antibiotics, chemotherapy agents, and nonsteroidal anti ...
Mariela Di Vanna, Nawal Aamir, Cristina Rodriguez Andujar, Adam Kaplan   +3 more
doaj   +1 more source

Reticuloendothelial cell function in autoimmune hemolytic anemia (AIHA): studies on the mechanism of peripheral monocyte activation. [PDF]

, 1985
We examined the activity of peripheral blood monocytes in patients with autoimmune hemolytic anemia (AIHA) using an in vitro assay of monocyte-macrophage interaction with erythrocytes and an antibody-dependent cell-mediated cytotoxicity (ADCC) assay. The
Ota, Zensuke, Sunada, Mitsutoshi, Suzuki, Shinya   +2 more
core   +1 more source

Severe autoimmune hemolytic anemia during pegylated interferon plus ribavirin treatment for chronic hepatitis C: a case report

Clinical Case Reports, 2017
Key Clinical Message We report a rare case of severe autoimmune hemolytic anemia triggered by pegylated interferon during combination therapy for chronic HCV.
Shasha Wang, Eryun Qin, Yixiao Zhi, Rui Hua   +3 more
doaj   +1 more source

Autoimmune hemolytic anemia: Case review

Anales de Pediatría (English Edition), 2021
Introduction: Autoimmune hemolytic anemia (AIHA) is a rare and generally self-limiting disease in children. Material and methods: A descriptive cross-sectional study was performed in children under 18 years diagnosed with AIHA from January 1997 to July ...
María Nazaret Sánchez, Josune Zubicaray, Elena Sebastián, Eva Gálvez, Julián Sevilla   +4 more
doaj   +1 more source

COVID-19 infection associated with autoimmune hemolytic anemia

Annals of Hematology, 2020
A 62-y-old man developed Covid-19 infection. Fourteen days after the first respiratory symptoms, he presented biological signs of hemolysis with cold agglutinins 1/16384.
A. Capes, S. Bailly, P. Hantson, L. Gérard, P. Laterre   +4 more
semanticscholar   +1 more source

Babesiosis-induced warm autoimmune hemolytic anemia, from infection to hemolysis: a case report

Journal of Medical Case Reports
Background Warm autoimmune hemolytic anemia is characterized by destruction of red blood cells mediated by autoantibodies, which can be triggered by various underlying factors including tick-borne infections. Babesia spp.
Jenna Davison, Jonah Kan, Jennifer Gile, Ubenthira Patgunarajah, Jeffry Degenhardt, Ronald Go, Jithma P. Abeykoon   +6 more
doaj   +1 more source

Immunotherapy-associated autoimmune hemolytic anemia

Journal for ImmunoTherapy of Cancer, 2017
Background Immunotherapy has been widely used in the treatment of several solid and hematologic malignancies. Checkpoint inhibitors have been the forefront of cancer immunotherapy in recent years.
Uqba Khan, Tarik Hadid, Farman Ali, Muhammad Siddique Khurram, Awais Zaka   +4 more
doaj   +1 more source

Prognostic significance of hemoglobin level and autoimmune hemolytic anemia in SARS-CoV-2 infection

Annals of Hematology, 2020
Higher levels of D-dimer, LDH, and ferritin, all have been associated with the poor prognosis of COVID-19. In a disease where there are acute inflammation and compromised oxygenation, we investigated the impact of initial hemoglobin (Hgb) levels at ...
Abdulrahman A. Algassim, Assem A Elghazaly, Abdulrahman S. Alnahdi, Owais M. Mohammed-Rahim, Abdulaziz Alanazi, N. A. Aldhuwayhi, Mashael Alanazi, Mohammed F. Almutairi, I. Aldeailej, Najeeb A. Kamli, M. Aljurf   +10 more
semanticscholar   +1 more source

IKAROS Associated Immunodeficiency and Thrombotic Thrombocytopenic Purpura

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Pathogenic variants in IKZF1 (IKAROS) are linked to immunodeficiency, malignancy, and immune dysregulation. We describe a family with a rare IKZF1 variant presenting with humoral immunodeficiency and thrombotic thrombocytopenic purpura (TTP). A non‐consanguineous family was clinically monitored; clinical, immunological, and genetic data (exome
Ilia Spivak, Daniella Magen, Karin Weiss, Tamar Paperna, Suhair Hanna, Amos Etzioni, Adi Miller‐Barmak, Yonatan Butbul Aviel   +7 more
wiley   +1 more source