Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Samar A. Al Nahhash"'
Autor:
Mohammed S. Alshahrani, Laila Perlas Asonto, Mohamed M. El Tahan, Amal H. Al Sulaibikh, Sukayna Z. Al Faraj, Abdullah A. Al Mulhim, Murad F. Al Abbad, Samar A. Al Nahhash, Moath N. Aldarweesh, Alaa M. Mahmoud, Nisreen Almaghraby, Mohammed A. Al Jumaan, Thamir O. Al Junaid, Faisal M. Al Hawaj, Samar AlKenany, Omaima F. ElSayed, Haitham M. Abdelwahab, Mohamed M. Moussa, Bader K. Alossaimi, Shaikah K. Alotaibi, Talal M. AlMutairi, Duaa A. AlSulaiman, Saad D. Al Shahrani, Donia Alfaraj, Waleed Alhazzani
Publikováno v:
Trials, Vol 20, Iss 1, Pp 1-7 (2019)
Abstract Background Sickle cell disease (SCD) is an inherited hematological disorder where the shape of red blood cells is altered, resulting in the destruction of red blood cells, anemia, and other complications. SCD is prevalent in the southern and
Externí odkaz:
https://doaj.org/article/958d0a5a3bc149ce8caca186a85e51b1
Autor:
Haitham M. Abdelwahab, Talal M. Almutairi, Abdullah A. Al Mulhim, Mohammed Alshahrani, Bader K. Alossaimi, Donia Alfaraj, Mohamed M. Moussa, Omaima F. ElSayed, Waleed Alhazzani, Samar AlKenany, Alaa M. Mahmoud, Amal H. Al Sulaibikh, Samar A. Al Nahhash, Duaa A. AlSulaiman, Laila Perlas Asonto, Sukayna Z. Al Faraj, Mohamed M. El Tahan, Faisal M. Al Hawaj, Murad F. Al Abbad, Mohammed A Al Jumaan, Saad D. Al Shahrani, Thamir O. Al Junaid, Shaikah K. Alotaibi, Moath N. Aldarweesh, Nisreen Almaghraby
Publikováno v:
Trials, Vol 20, Iss 1, Pp 1-7 (2019)
Trials
Trials
Background Sickle cell disease (SCD) is an inherited hematological disorder where the shape of red blood cells is altered, resulting in the destruction of red blood cells, anemia, and other complications. SCD is prevalent in the southern and eastern