نتایج جستجو برای: prothrombin g20210a

تعداد نتایج: 7182  

Journal: :Haematologica 2003
Ida Martinelli Emanuela Taioli Guido Ragni Paolo Levi-Setti Serena Maria Passamonti Tullia Battaglioli Corrado Lodigiani Pier Mannuccio Mannucci

BACKGROUND AND OBJECTIVES Women undergoing assisted reproductive procedures, such as in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI), fail to achieve pregnancy in approximately 70% of cases. Postulating that among the possible causes of failure of embryo implantation might be an impairment of the uteroplacental circulation due to hypercoagulability in the mother, we inv...

Journal: :Thrombosis and haemostasis 2009
Alessandro Pezzini Mario Grassi Elisabetta Del Zotto Alessia Giossi Irene Volonghi Paolo Costa Armin Grau Mauro Magoni Alessandro Padovani Christoph Lichy

Conflicting results are available on the association of prothrombotic genetic abnormalities with patent foramen ovale (PFO)-related cerebral ischaemia. We comprehensively sought and identified studies of the association of both the factor V Leiden (FV(G1691A) mutation) and the prothrombin mutation (PT(G20210A) mutation) with PFO-related cerebral ischaemia and did meta-analyses to assess the evi...

2014
Samer Bani-Hani Omar Siddiqui Anami Patel Arif Showkat

Venous thromboembolism (VTE) represents the formation of a blood clot in one of the deep veins of human body. The significant morbidity and mortality rates associated with VTE have spurred increasing investigations seeking to identify causative factors for this complex condition. While the most frequent causes of an inherited hypercoagulable state are the Factor V Leiden mutation and the prothr...

Journal: :Blood 1999
U Nowak-Göttl C Wermes R Junker H G Koch R Schobess G Fleischhack D Schwabe S Ehrenforth

The reported incidence of thromboembolism in children with acute lymphoblastic leukemia (ALL) treated with L-asparaginase, vincristine, and prednisone varies from 2.4% to 11.5%. The present study was designed to prospectively evaluate the role of the TT677 methylenetetrahydrofolate reductase (MTHFR) genotype, the prothrombin G20210A mutation, the factor V G1691A mutation, deficiencies of protei...

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