Results 1 to 10 of about 48,507 (298)

Idiopathic thrombocytopenic purpura

Contemporary Clinical Dentistry, 2014
Idiopathic thrombocytopenic purpura (ITP) is defined as a hematologic disorder, characterized by isolated thrombocytopenia without a clinically apparent cause.
L Kayal, S Jayachandran, Khushboo Singh
doaj   +6 more sources

Sequential occurrence of thrombotic thrombocytopenic purpura, essential thrombocythemia, and idiopathic thrombocytopenic purpura in a 42-year-old African-American woman: a case report and review of the literature

Journal of Medical Case Reports, 2012
Introduction Thrombotic thrombocytopenic purpura and idiopathic thrombocytopenic purpura are two well recognized syndromes that are characterized by low platelet counts. In contrast, essential thrombocythemia is a myeloproliferative disease characterized
Farhat Mirna H, Kuriakose Philip, Jawad Michael, Hanbali Amr   +3 more
doaj   +2 more sources

Idiopathic Thrombocytopenic Purpura and the Moderna Covid-19 Vaccine. [PDF]

Ann Emerg Med, 2021
Julian JA, Mathern DR, Fernando D.
europepmc   +2 more sources

Thrombocytopenia: diagnosis with flow cytometry and antiplatelet antibodies [PDF]

Einstein (São Paulo), 2011
Objective: To identify antiplatelet antibodies by flow cytometry (direct method) in patients with thrombocytopenia. Methods: Between January 1997 and March 2004 a total of 15100 patients were referred to the Centro de Hematologia de São Paulo for ...
João Carlos de Campos Guerra, Ruth Hissae Kanayama, Sonia Tsukasa Nozawa, Márcia Regina Ioshida, Irina Yoko Takiri, Robson José Lazaro, Nelson Hamerschlak, Luiz Gastão Mange Rosenfeld, Celso Carlos de Campos Guerra, Nydia Strachman Bacal   +9 more
doaj   +3 more sources

Childhood idiopathic thrombocytopenic purpura [PDF]

The Lancet, 1997
HP Davis, A Raffles
openalex   +4 more sources

Idiopathic thrombocytopenic purpura in a patient with situs inversus totalis: case report and literature review

Einstein (São Paulo), 2020
Situs inversus totalis is a rare recessive autosomal congenital abnormality in which the mediastinal and abdominal organs are in a mirrored position when compared to the usual topography.
Carolina Rodrigues Dal Bo, Beatriz Piovesana Devito, Leticia Piovesana Devito, Gabriella Paes del Papa, Nelson Hamerschlak   +4 more
doaj   +2 more sources

Idiopathic thrombocytopenic purpura [PDF]

Current Paediatrics, 1995
Idiopathic thrombocytopenic purpura in children usually a self limiting disorder. It may follow a viral infection or immunisation and is caused by an inappropriate response of the immune system. About 20-30% of children will fail to remit over six months (chronic idiopathic thrombocytopenic purpura).
openaire   +6 more sources

IDIOPATHIC TROMBOCYTOPENIC PURPURA DURING PREGNANCY.OBSTETRICS AND PERENATAL RISKS

Акушерство, гинекология и репродукция, 2016
Idiopathic thrombocytopenic purpura is a relatively rare disease, especially during pregnancy. Currently, there are many ways of diagnostics, monitoring and treatment of patients.
V. B. Tskhay, E. K. Grebennikova
doaj   +1 more source

Idiopathic thrombocytopenic purpura: a practice guideline developed by explicit methods for the American Society of Hematology.

Blood, 1996
DIOPATHIC thrombocytopenic purpura (ITP, also I known as primary immune thrombocytopenic purpura) is a hematologic disorder for which appropriate diagnostic and treatment strategies are uncertain.
J. George, S. Woolf, G. Raskob, J. Wasser, L. Aledort, P. Ballem, V. Blanchette, J. Bussel, D. Cines, J. Kelton, A. Lichtin, R. Mcmillan, J. Okerbloom, D. H. Regan, I. Warrier   +14 more
semanticscholar   +1 more source

Idiopathic thrombocytopenic purpura (ITP) – new era for an old disease

Romanian journal of internal medicine = Revue roumaine de medecine interne, 2019
Immune thrombocytopenia is an autoimmune hematological disorder characterized by severely decreased platelet count of peripheral cause: platelet destruction via antiplatelet antibodies which may also affect marrow megakaryocytes.
M. Onisâi, A. Vlădăreanu, Andreea Spînu, M. Găman, H. Bumbea   +4 more
semanticscholar   +1 more source