نتایج جستجو برای: idiopathic thrombocytopenic purpura itp

تعداد نتایج: 74273  

Journal: :Blood 1984
J Pizzuto R Ambriz

In order to analyze the usefulness of different types of treatment in relation to the interval since the onset of idiopathic thrombocytopenic purpura (ITP), a collaborative study of 934 adult patients was undertaken. Prednisone was administered to 818 patients, and 32% of them achieved prolonged complete remission (PCR). However, only 14% of patients who had ITP for more than six months achieve...

2001
Jane C. Moore Catherine P. M. Hayward Theodore E. Warkentin John G. Kelton

Recent studies investigating thrombotic thrombocytopenic purpura (TTP) have implicated abnormal plasma von Willebrand factor (vWF)-cleaving metalloprotease activity in this disorder. It has been proposed that a metalloprotease cleaves unusually large (UL) multimers of vWF, which enter the circulation from the endothelium. Abnormal metalloprotease activity could result in ULvWF, which could part...

جان بابایی, قاسم , عابدیان کناری, سعید , علیزاده, احد , علیزاده, نیره , کرمی, حسین ,

Background: Immune Thrombocytopenic Purpura (ITP) is an acquired autoimmune disorder characterized by a low platelet count because of anti platelet auto-antibodies. ITP patients have auto antibodies against platelet antigens. T CD4+ lymphocytes are effective cells in immune system that has an important role in auto reactive antibody production and class switching. The pathophisiology and mechan...

Journal: :iranian journal of blood and cancer 0
m faranoush kh arjmandi rafsanjani z sadr aa hedayatiasl a mehrvar

background:chronic idiopathic thrombocytopenic purpura (itp) is an autoimmune disorder characterized by a low platelet count due to reduced production and higher destruction of the platelets. therapy is aimed at increasing the patient’s platelet count to safe levels and includes a wide variety of treatments, which has a large impact on the patient’s quality of life. health related quality of li...

Journal: :The oncologist 2009
Terry Gernsheimer

The mechanism of idiopathic (autoimmune) thrombocytopenic purpura (ITP) has historically been attributed to platelet autoantibody production and the resultant platelet destruction. More recent evidence suggests a multifactorial pathogenesis. A complex picture of the immune processes involved in autoimmunity has emerged over the last decade with the identification and characterization of immunor...

Journal: :Blood 1975
I Branehög J Kutti B Ridell B Swolin A Weinfeld

In 23 patients with untreated idiopathic thrombocytopenic purpura (TP), the relation of thrombokinetics to quantitative determinations of megakaryocytes in bone marrow sections was studied. The megakaryocytes were classified into maturation stages, and platelet sizes were determined. Megarkaryocyte number and volume per microliter of bone marrow were significantly higher in ITP as compared to c...

Journal: :Blood 1996
R V Emmons D M Reid R L Cohen G Meng N S Young C E Dunbar N R Shulman

Thrombopoietin (TPO), the ligand for c-mpl, stimulates proliferation of committed megakaryocytic progenitors and induces maturation of megakaryocytes. To better understand factors regulating TPO levels, we measured blood levels of TPO in patients with impaired platelet production due to aplastic anemia (AA) and with platelet destructive disorders, including idiopathic thrombocytopenic purpura (...

Journal: :British journal of haematology 2008
Bernadette Garvey

Current treatment regimens for haematological autoimmune diseases are relatively non-selective and are often associated with considerable toxicity. Recently, it has become clear that B cells play a key role in both the development and perpetuation of autoimmunity, suggesting that B-cell depletion could be a valuable treatment approach for patients with autoimmune diseases. This article reviews ...

Journal: :Blood 2001
J C Moore C P Hayward T E Warkentin J G Kelton

Recent studies investigating thrombotic thrombocytopenic purpura (TTP) have implicated abnormal plasma von Willebrand factor (vWF)-cleaving metalloprotease activity in this disorder. It has been proposed that a metalloprotease cleaves unusually large (UL) multimers of vWF, which enter the circulation from the endothelium. Abnormal metalloprotease activity could result in ULvWF, which could part...

Journal: :iranian journal of pediatric hematology and oncology 0
sh nazari department of pediatric hematology and oncology, mofid children’s hospital, shahid beheshti university of medical scienc f abdollah gorji - clinical research development center, mofid children’s hospital, shahid beheshti university of medical sciences, tehraسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) mt sadeghi-koupai faculty of pharmacy, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)

abstract background immune thrombocytopenic purpura (itp) is a common autoimmune bleeding condition in children that is characterized by a decrease in the platelet count. the aims of this study were to define epidemiologic features of patients with primary itp who were admitted to mofid children's hospital, tehran, iran, in a 5-year period. methods we retrospectively studied the records of pati...

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