نتایج جستجو برای: glanzmanns thrombasthenia

تعداد نتایج: 525  

Journal: :The Journal of clinical investigation 1987
A T Nurden J P Rosa D Fournier C Legrand D Didry A Parquet D Pidard

Patient C.M. presented platelet function defects symptomatic of Glanzmann's thrombasthenia. However, analysis of surface-labeled platelets by SDS-polyacrylamide gel electrophoresis revealed the usual presence of the major glycoproteins, including GP IIb and GP IIIa. Platelet fibrinogen was not detected. Analysis of Triton X-100 extracts of Ca2+-washed C.M. platelets by crossed immunoelectrophor...

Journal: :American Journal of Laboratory Medicine 2018

Journal: :Sri Lanka Journal of Child Health 2020

2001
Rivka Yatuv Nurit Rosenberg Ariella Zivelin Hava Peretz Rima Dardik Luba Trakhtenbrot Uri Seligsohn

http://bloodjournal.hematologylibrary.org/content/98/4/1063.full.html Updated information and services can be found at: (2497 articles) Hemostasis, Thrombosis, and Vascular Biology • Articles on similar topics can be found in the following Blood collections http://bloodjournal.hematologylibrary.org/site/misc/rights.xhtml#repub_requests Information about reproducing this article in parts or in ...

Journal: :SN Comprehensive Clinical Medicine 2022

Glanzmann’s thrombasthenia (GT) is an uncommon congenital disease due to a qualitative or quantitative anomaly of the glycoprotein complex GPIIb/IIIA, resulting in defective platelet aggregation. In pregnant women, this bleeding disorder could lead severe haemorrhages and may require aggressive treatment with combined therapy, including concentrates, anti-fibrinolytics recombinant activated coa...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید