Results 101 to 110 of about 54,639 (294)

Dissecting the pathophysiology of immune thrombotic thrombocytopenic purpura: interplay between genes and environmental triggers

Haematologica, 2018
Although outstanding progress has been made in understanding the pathophysiology of thrombotic thrombocytopenic purpura (TTP), knowledge of the immunopathogenesis of the disease is only at an early stage. Anti-ADAMTS13 auto-antibodies were shown to block
J. Hrdinova, Silvia D’Angelo, Nuno A G Graça, Bogac Ercig, K. Vanhoorelbeke, A. Veyradier, J. Voorberg, P. Coppo   +7 more
semanticscholar   +1 more source

Anti-RH immunoglobulin therapy for human immunodeficiency virus-related immune thrombocytopenic purpura [PDF]

, 1988
Éric Oksenhendler, P Bierling, Y. Brossard, C Schenmetzler, PM Girard, M Séligmann, JP Clauvel   +6 more
openalex   +3 more sources

Systemic lupus erythematosus presenting with thrombocytopenia. Report of a child with positive anticardiolipin antibodies

The Turkish Journal of Pediatrics, 1996
We report a case of systemic lupus erythematosus initially presenting with thrombocytopenia and diagnosed as immune thrombocytopenic purpura.
G Kanra, G Erdem, S Ozen, F Y Anlar, N Beşbaş, M Ceyhan   +5 more
doaj  

Cytomegalovirus-Related Immune Thrombocytopenic Purpura in an Immunocompetent Adult

Annals of Internal Medicine: Clinical Cases
We present the case of a 42-year-old immunocompetent man who was diagnosed with acute immune thrombocytopenic purpura and had evidence of an acute cytomegalovirus infection, concerning for secondary immune thrombocytopenic purpura.
Derek J. Essegian, Rachel A. Sibley
doaj   +1 more source

Immune thrombocytopenic purpura in a child with mucopolysaccharidoses

Journal of Applied Hematology, 2020
Hematological manifestations in mucopolysaccharidoses (MPS) are relatively rare. We report a rare presentation of immune thrombocytopenic purpura with recurrent mucosal bleeds in a 5-year-old boy with MPS.
Nikhil Rajvanshi, Manish Kumar
doaj   +1 more source

Variant clinical courses in children with immune thrombocytopenic purpura: Sixteen year experience of a single medical center [PDF]

, 2010
Objective: Immune thrombocytopenic purpura (ITP) is the most common cause of acquired thrombocytopenia in children. The objective of this study was to evaluate the presenting features, variation in the clinical courses, initial response rate to therapy ...
Berna Atabay, Esra Arun Özer, Haldun Öniz, İkbal Durak, Işın Yaprak, Meral Türker   +5 more
core  

Acute immune thrombocytopenic purpura in an adolescent with 2009 novel H1N1 influenza A virus infection [PDF]

, 2011
Although both leukopenia and thrombocytopenia are not uncommon hematological findings among patients with novel 2009 H1N1 influenza virus infection, immune thrombocytopenic purpura has rarely been shown to be associated with this novel influenza A ...
Chan, Yu-Jiun, Chen, Po-Yen, Chou, Teh-Ying, Lee, Chun-Yi, Wu, Meng-Che   +4 more
core   +2 more sources

Prognostic factors and long‐term outcome in dogs diagnosed with primary and secondary immune thrombocytopenia in Ireland

Journal of Small Animal Practice, Volume 66, Issue 5, Page 305-313, May 2025.
Objectives The objectives of this study were to describe the outcome and prognostic factors in dogs diagnosed with primary and secondary immune thrombocytopenia (ITP). Materials and Methods Medical records of dogs diagnosed with primary and secondary ITP in a referral hospital in Ireland were retrospectively evaluated.
E. López‐Bailén, A. Duclos, D. Mullany, K. Le Boedec, B. Cuq   +4 more
wiley   +1 more source

Immunomodulatory treatments for persistent and chronic immune thrombocytopenic purpura

Medicine, 2017
Background Corticosteroid sparing is required in 15% to 40% of adults with persistent or chronic primary immune thrombocytopenic purpura (ITP). Herein, the efficacy of immunomodulatory drugs (dapsone, interferon alpha, danazol, and hydroxychloroquine as ...
E. Weber, Q. Reynaud, R. Fort, S. Durupt, P. Cathébras, I. Durieu, J. Lega   +6 more
semanticscholar   +1 more source

Prevalence of Immune Thrombocytopenia Purpura in Wasit Province

Wasit Journal for Pure Sciences
A lower than normal platelet count is a hallmark of the acquired autoimmune disease immune thrombocytopenic purpura (ITP). This autoimmune disease is characterized by low platelet counts, purpura, and hemorrhagic episodes caused by antiplatelet ...
Rawan Alaa
doaj   +1 more source