نتایج جستجو برای: autoimmune thrombocytopenia

تعداد نتایج: 84689  

Background: Evans syndrome is an uncommon autoimmune disorder manifested by fatigue, jaundice, pallor, purpura and petechiae. The main characteristics of this rare disease are simultaneous or sequential existence of positive anti-globulin test, immune thrombocytopenia (ITP) and autoimmune hemolytic anemia (AIHA). Evans syndrome as an autoimmune disorder can be associated with other diseases. Th...

Journal: :Blood 1997
M Dreyfus C Kaplan E Verdy N Schlegel I Durand-Zaleski G Tchernia

Thrombocytopenia is a common condition in distressed newborns, but little is known about thrombocytopenia in an unselected cohort of neonates. In an attempt to address this issue, a multicenter prospective study was conducted in three obstetrical wards of AP-HP in Paris. We found the frequency of neonatal thrombocytopenia (<150 x 10(9)/L) to approximate 0.9% (48 of 5,632 appropriate samples). A...

Journal: :Haematologica 2010
Ameet Sarpatwari Dimitri Bennett John W Logie Amit Shukla Kathleen J Beach Adrian C Newland Simon Sanderson Drew Provan

BACKGROUND The risk of thromboembolic events in adults with primary immune thrombocytopenia has been little investigated despite findings of increased susceptibility in other thrombocytopenic autoimmune conditions. The objective of this study was to evaluate the risk of thromboembolic events among adult patients with and without primary immune thrombocytopenia in the UK General Practice Researc...

2014
Paola Giordano Giuseppe Lassandro Maria Sangerardi Maria Felicia Faienza Federica Valente Baldassarre Martire

Kabuki syndrome (also called Niikawa-Kuroki syndrome) is a rare genetic disease described for the first time in Japan, characterised by anomalies in multiple organ systems and often associated with autoimmune disorders and impaired immune response. We herein report the clinical history, the therapeutic approach and the outcome of two children with Kabuki syndrome who developed autoimmune haemat...

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