Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Meteb A. Ahmed"'
Autor:
Husain Y Alkhaldy, Bandar S Asiri, Meteb A Ahmed, Sabah A Khozam, Abdulbari A Alzahrani, Yahya M Alqahtani, Nouf D Alshamrani, Omayma S Bakheet
Publikováno v:
Saudi Journal for Health Sciences, Vol 10, Iss 1, Pp 38-42 (2021)
Background: Sickle cell disease is a common hereditary hemoglobin disorder in southern Saudi Arabia. The current models of health care provision and health service utilization are not homogeneous across the kingdom. Aim: The current models of health
Externí odkaz:
https://doaj.org/article/dc82cb4cee1d43d8bb3e09cf6f5cb468
Autor:
Husain Y. Alkhaldy, Mohammed Alqahtani, Zainab S. Alamri, Nuha A. Althibait, Meteb A. Ahmed, Mohammed A. Alzahrani, Omayma S. Bakheet, Shahid Aziz
Publikováno v:
Saudi Pharmaceutical Journal, Vol 28, Iss 8, Pp 905-910 (2020)
Folate, also known as vitamin B9, is a co-factor necessary for DNA synthesis. Folate deficiency is associated mainly with hematological findings including megaloblastic anemia and pancytopenia. Many countries have mandated grain fortification with mi
Externí odkaz:
https://doaj.org/article/c6e333e25ea04d1c963045bc7dd0a160
Autor:
Mohammed A. Alzahrani, Omayma S. Bakheet, Husain Y Alkhaldy, Meteb A. Ahmed, Zainab S. Alamri, Nuha A. Althibait, Mohammed Alqahtani, Shahid Aziz
Publikováno v:
Saudi Pharmaceutical Journal, Vol 28, Iss 8, Pp 905-910 (2020)
Saudi Pharmaceutical Journal : SPJ
Saudi Pharmaceutical Journal : SPJ
Folate, also known as vitamin B9, is a co-factor necessary for DNA synthesis. Folate deficiency is associated mainly with hematological findings including megaloblastic anemia and pancytopenia. Many countries have mandated grain fortification with mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::356d057bd551e335bd14a2429f114213
http://www.sciencedirect.com/science/article/pii/S1319016420301298
http://www.sciencedirect.com/science/article/pii/S1319016420301298
Autor:
Bandar S Asiri, Nouf D Alshamrani, Abdulbari Ahmed Alzahrani, Yahya M Alqahtani, Meteb A. Ahmed, Husain Y Alkhaldy, Omayma S. Bakheet, Sabah A Khozam
Publikováno v:
Saudi Journal for Health Sciences, Vol 10, Iss 1, Pp 38-42 (2021)
Background: Sickle cell disease is a common hereditary hemoglobin disorder in southern Saudi Arabia. The current models of health care provision and health service utilization are not homogeneous across the kingdom. Aim: The current models of health
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7e14286e1c8cb8451b29d48e48d6cb8
https://doi.org/10.4103/sjhs.sjhs_228_20
https://doi.org/10.4103/sjhs.sjhs_228_20