Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mohammed Khalid Alabdulaali"'
Autor:
Mansour S Aljabry, Abdulaziz Alhoshan, Fahad Alrawaf, Abdullah Alhowidi, Abdullah Alsahli, Saad Alrubaia, Abdulmajeed Alshaikh, Adnan Alkhayat, Mohammed Khalid Alabdulaali
Publikováno v:
Journal of Applied Hematology, Vol 10, Iss 3, Pp 84-87 (2019)
BACKGROUND: Sickle cell anemia and glucose-6-phosphate dehydrogenase deficiency (G6PD) are the most common causes of inherited hemolytic anemia in Saudi Arabia. Due to high prevalence, some blood transfusion services perform routine blood donor scree
Externí odkaz:
https://doaj.org/article/ba276040faf44fc1a89fa2ac718b2439
Autor:
Mohammed Khalid Alabdulaali
Publikováno v:
Hematology Reports, Vol 1, Iss 1, Pp e10-e10 (2009)
In 2005, an activating mutation in the Janus kinase 2 (JAK2) was identified in a significant proportion of patients with myeloproliferative neoplasms, mainly polycythemia vera, essential thrombocythemia and primary myelofibrosis. Many types of mutati
Externí odkaz:
https://doaj.org/article/8a4df77664954b7eb6d19b4469ade3d2
Autor:
Abdullah Alhowidi, Saad Alrubaia, Abdulaziz Alhoshan, Mansour S. Aljabry, Abdullah Alsahli, Adnan Alkhayat, Mohammed Khalid Alabdulaali, Fahad Alrawaf, Abdulmajeed Alshaikh
Publikováno v:
Journal of Applied Hematology, Vol 10, Iss 3, Pp 84-87 (2019)
BACKGROUND: Sickle cell anemia and glucose-6-phosphate dehydrogenase deficiency (G6PD) are the most common causes of inherited hemolytic anemia in Saudi Arabia. Due to high prevalence, some blood transfusion services perform routine blood donor scree