Results 91 to 100 of about 26,471 (221)
Background Thrombotic thrombocytopenic purpura is a very rare hereditary blood deficiency disorder of ADAMTS13 (von Willebrand factor-cleaving protease) and a life-threatening thrombotic microangiopathy characterized by thrombocytopenia and ...
Valter Romão de Souza +9 more
doaj +1 more source
Microbial risk factors of cardiovascular and cerebrovascular diseases: potential therapeutic options [PDF]
Infection and inflammation may have a crucial role in the pathogenesis of atherosclerosis. This hypothesis is supported by an increasing number of reports on the interaction between chronic infection, inflammation, and atherogenesis.
Abbas, M.A. +6 more
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Idiopathische thrombozytopenische Purpura im Kindesalter [PDF]
Zusammenfassung: Die idiopathische thrombozytopenische Purpura (ITP) ist eine Blutungskrankheit, die durch eine verkürzte Lebensdauer der Thrombozyten charakterisiert ist.
Imbach, P., Kühne, T.
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Idiopathic Thrombocytopenic Purpura Misdiagnosed as Hereditary Angioedema [PDF]
Hereditary angioedema is a rare, but potentially life-threatening genetic disorder that results from an autosomal dominant trait. It is characterized by acute, recurrent attacks of severe local edema, most commonly affecting the skin and mucosa. Swelling
Andersen, Michelle Fog, Bygum, Anette
core +5 more sources
Idiopathic thrombocytopenic purpura: current concepts in pathophysiology and management. [PDF]
Idiopathic thrombocytopenic purpura (ITP) is characterized by a low platelet count, which is the result of both increased pla- telet destruction and insufficient platelet production.
Amadori, S +5 more
core +1 more source
Modern concepts of the platelet in health and disease [PDF]
Thesis (M.D.)--Boston ...
Estes, J. Worth
core
The relationship between self-esteem and quality of life of patients with idiopathic thrombocytopenic purpura at Isfahan’s Sayed Al-Shohada Hospital, Iran, in 2013 [PDF]
Background: Idiopathic thrombocytopenic purpura (ITP) is a chronic disease which is accompanied with hopelessness and loss of the sense of well-being due to its symptoms and treatment.
Hemati, Z., Kiani, D.
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Fei Lv,1,2 Yue Zhao,2 Xing-Di Yang,2 Han-Zhu Chen,2 Wen-Ya Ren,2 Ling-Xia Chen,2 Qiao-Qiao Yi,2 Wei Zheng,2 Hong-Ying Pan2 1The Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, 310053, People’s Republic of China ...
Lv F +8 more
doaj
Successful use of rituximab in Evans syndrome and refractory immune thrombocytopenic purpura [PDF]
Immune cytopenias are mediated by auto-antibodies produced by B-lymphocytes. Conventional treatment of immune-mediated haematological disorders includes immunosuppression with steroids and other immune modulating therapies and in some refractory cases ...
Adil, Salman Naseem +3 more
core +1 more source

