Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Fadel M Ragab"'
Autor:
Mohammad Athar PhD, Zainularifeen Abduljaleel PhD, Ibrahim S. Ghita MD, Amani A. Albagenny MD, Saeed H. Halawani PhD, Mohammad M. Alkazmi MD, Wafa M. Elbjeirami PhD, Khalid Alquthami PhD, Mohammad M. Alkhuzae BLM, Fadel M. Ragab MS, Faisal A. Al-Allaf PhD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
The rare Gln534 (Factor V Leiden; FVL) allele (1:169,519,049 T>C) is associated with an increased risk of venous thrombosis. The purpose of this study was to measure the prevalence of Factor V Leiden mutation in thrombophilia patients with deep vein
Externí odkaz:
https://doaj.org/article/e394647bb9664e38a5acbaa68b2fea43
Autor:
Saeed H. Halawani, Mohammad Athar, Mohammad M. Alkhuzae, Zainularifeen Abduljaleel, Ibrahim S. Ghita, Mohammad M. Alkazmi, Fadel M Ragab, Khalid Alquthami, Faisal A. Al-Allaf, Amani A. Albagenny, Wafa M. Elbjeirami
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
The rare Gln534 (Factor V Leiden; FVL) allele (1:169,519,049 T>C) is associated with an increased risk of venous thrombosis. The purpose of this study was to measure the prevalence of Factor V Leiden mutation in thrombophilia patients with deep vein