Results 11 to 20 of about 14,442 (233)

Idiopathic Thrombocytopenic Purpura after Mastectomy and Axillary Lymph Node Dissection

open access: yesCase Reports in Surgery, 2014
First described in 1916, idiopathic thrombocytopenic purpura (ITP) is an autoimmune disease resulting in the destruction of platelets. Here, we present a case of an 85-year-old patient diagnosed with invasive ductal carcinoma of the breast whose surgical
Wil L. Santivasi   +2 more
doaj   +1 more source

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

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

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

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   +4 more sources

Neural Feature Selection for Learning to Rank [PDF]

open access: yesarXiv, 2021
LEarning TO Rank (LETOR) is a research area in the field of Information Retrieval (IR) where machine learning models are employed to rank a set of items. In the past few years, neural LETOR approaches have become a competitive alternative to traditional ones like LambdaMART.
arxiv  

Learning to Rank from Relevance Judgments Distributions [PDF]

open access: yesarXiv, 2022
Learning to Rank (LETOR) algorithms are usually trained on annotated corpora where a single relevance label is assigned to each available document-topic pair. Within the Cranfield framework, relevance labels result from merging either multiple expertly curated or crowdsourced human assessments.
arxiv  

Púrpura trombocitopênica imunológica como manifestação inicial de lúpus eritematoso sistêmico juvenil Idiopathic thrombocytopenic purpura as initial manifestation of juvenile systemic lupus erythematosus

open access: yesRevista Brasileira de Reumatologia, 2003
Os pacientes com púrpura trombocitopênica imunológica apresentam risco aumentado para desenvolver lúpus eritematoso sistêmico, principalmente quando a doença evolui de forma crônica. Alguns autores observaram que o sexo feminino, a idade mais avançada, a
Josefina Aparecida Pellegrini Braga   +3 more
doaj   +1 more source

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

Multiple domains of ADAMTS13 are targeted by autoantibodies against ADAMTS13 in patients with acquired idiopathic thrombotic thrombocytopenic purpura

open access: yesHaematologica, 2010
Background Type G immunoglobulins against ADAMTS13 are the primary cause of acquired (idiopathic) thrombotic thrombocytopenic purpura. However, the domains of ADAMTS13 which the type G anti-ADAMT13 immunoglobulins target have not been investigated in a ...
X. Long Zheng   +7 more
doaj   +1 more source

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