Results 21 to 30 of about 46,023 (268)

Adult Idiopathic Thrombocytopenic Purpura

open access: yesHematology, 2003
Idiopathic thrombocytopenic purpura (ITP) in adults is an autoimmune disorder characterised by persistent thrombocytopenia due to autoantibodies directed against platelet antigens. There have been major advances in our understanding of the pathophysiology of ITP and an increasing number of diagnostic tests and treatments available.
Mead, A, Newland, A, Provan, D
openaire   +3 more sources

Manajemen Anestesi pada Seksio Sesarea dengan Idiopathic Thrombocytopenic Purpura: Serial kasus

open access: yesJurnal Anestesi Obstetri Indonesia, 2021
Trombositopenia merupakan perubahan hemostasis yang umum terjadi pada wanita hamil, namun jarang ditemukan kondisi berat. Idiopathic thrombocytopenic purpura (ITP) merupakan salah satu penyebab trombositopenia pada wanita hamil.
Achmad Haryanto   +2 more
doaj   +1 more source

Pregnancy and Birth Outcomes among Women with Idiopathic Thrombocytopenic Purpura

open access: yesJournal of Pregnancy, 2016
Objective. To examine pregnancy and birth outcomes among women with idiopathic thrombocytopenic purpura (ITP) or chronic ITP (cITP) diagnosed before or during pregnancy. Methods. A linkage of mothers and babies within a large US health insurance database
D. Wyszynski   +7 more
semanticscholar   +1 more source

Immune Thrombocytopenia as a Consequence of Rocky Mountain Spotted Fever

open access: yesCase Reports in Oncology, 2017
Primary immune thrombocytopenia (ITP) – also called idiopathic thrombocytopenic purpura or immune thrombocytopenic purpura – is an acquired thrombocytopenia caused by autoantibodies against platelet antigens.
Cherisse Baldeo   +2 more
doaj   +1 more source

Pathogenicity of anti-ADAMTS13 autoantibodies in acquired thrombotic thrombocytopenic purpura. [PDF]

open access: yes, 2015
BACKGROUND: Acquired thrombotic thrombocytopenic purpura (TTP) is an autoimmune disease in which anti-ADAMTS13 autoantibodies cause severe enzyme deficiency.
Crawley, JT   +3 more
core   +2 more sources

Post-Partum Thrombotic Thrombocytopenic Purpura (TTP) in a Patient with known Idiopathic (Immune) Thrombocytopenic Purpura: a case report and review of the literature

open access: yesJournal of Medical Case Reports, 2018
BackgroundIncidences of immune thrombocytopenic purpura occur in 1 in every 1000–10,000 pregnancies accounting for 3% of all thrombocytopenic pregnancies.
Naser Al-husban, O. Al-kuran
semanticscholar   +1 more source

Changes in Follicular Helper T Cells in Idiopathic Thrombocytopenic Purpura Patients

open access: yesInternational Journal on Biological Sciences, 2015
Background: Idiopathic thrombocytopenic purpura (ITP) is a primary autoimmune disease with a decreased platelet count caused by platelet destruction mediated mainly by platelet antibodies. T follicular helper (TFH) cells have demonstrated important roles
Jue Xie   +8 more
semanticscholar   +1 more source

Guidelines on the treatment of primary immune thrombocytopenia in children and adolescents: Associacao Brasileira de Hematologia, Hemoterapia e Terapia Celular Guidelines Project: Associacao Medica Brasileira - 2012 [PDF]

open access: yes, 2013
Centro de Hematologia de São PauloUniversidade Federal de São Paulo (UNIFESP) Escola Paulista de MedicinaCentro Infantil BoldriniUniversidade de São Paulo Faculdade de MedicinaAssociacao Medica BrasileiraHospital Ana CostaCentro de Hematologia e ...
Bernardo, Wanderley Marques   +5 more
core   +1 more source

Idiopathic Thrombocytopenic Purpura (ITP) [PDF]

open access: yesActa Haematologica, 1980
Sir.—I read with interest the article by Movassaghi et al entitled "Antiplatelet Antibodies in Childhood Idiopathic Thrombocytopenic Purpura" (Journal133:257-259, 1979). However, I cannot agree with their conclusion that platelet antibody usually disappears with recovery from thrombocytopenia in childhood ITP. We have already shown in three chronic and
openaire   +2 more sources

Idiopathic thrombocytopenic purpura

open access: yesJapanese Journal of Thrombosis and Hemostasis, 2008
Point(1)診断は血小板減少をきたす他の疾患の除外を基本とする.(2)血小板数と出血症状の程度,背景因子やライフスタイルに基づいて治療適応を決める.(3)治療はまずステロイド療法,次いで摘脾を行う.(4)ITPと診断されればまずH. pyloriを検索し,陽性であれば除菌療法を優先する.
openaire   +3 more sources

Home - About - Disclaimer - Privacy