Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ahmad Magablah"'
Autor:
Kamal F Akl, Abdul Karim Qudah, Abdalla Awidi, Mohammad Jaber Suleiman, Nidaa Ababneh, Nazzal Bsoul, Ahmad Magablah
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 25, Iss 6, Pp 1304-1307 (2014)
Externí odkaz:
https://doaj.org/article/b54f1175b7994fe091b9fe663fc9098b
Autor:
Abdul Karim Qudah, Nazzal Bsoul, Ahmad Magablah, Kamal F. Akl, Nidaa A. Ababneh, Abdalla Awidi, Mohammad Jaber Suleiman
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 25, Iss 6, Pp 1304-1307 (2014)
Autor:
Eyad Arafat, Abdalla Awidi, Ayed O. Ayed, Lena Marie, Mohammad Dweiri, Ahmad Magablah, Mohammad Ramahi, Nazzal Bsoul, Mohammad Bishtawi, Razan Mefleh
Publikováno v:
Leukemia Research. 34:1573-1575
One hundred and three patients with Philadelphia chromosome or BCR-ABL positive chronic myeloid leukemia (CML) in chronic phase who were on oral imatinib were included in this study. The study aimed to assess the relationship between imatinib trough
Autor:
M. Falah, S. Fauori, S. Swaidan, Razan Mefleh, M. Bishtawi, E. Arafat, Nazzal Bsoul, Dana Alhattab, M. Ramahi, M. Barqawi, Ahmad Magablah, M. Dweiri, Abdelhalim Awidi, E. Haddadeen, B. Tarawneh
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 16(1)
Summary. Haemophilia A (HA) is an X-linked recessive bleeding disorder caused by mutations in the factor VIII gene (F8), which encodes factor VIII (FVIII) protein, a plasma glycoprotein, that plays an important role in the blood coagulation cascade.
Publikováno v:
Journal of thrombosis and thrombolysis. 28(3)
Venous Thrombo-Embolism (VTE) is a serious complication in hospitalized patients but can be preventable. This prospective study addresses risk factors assessment and the use of heparin in this population. About 2,496 non pediatric patients were admit
FIX mutation spectrum in haemophilia B patients from Jordan: identification of three novel mutations
Autor:
Dana Alhattab, Ahmad Magablah, Razan Mefleh, Abdelhalim Awidi, M. Dweiri, A. S. Fauori, Nazzal Bsoul
Publikováno v:
Haemophilia. 17:162-163