Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Moath N. Aldarweesh"'
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
Autor:
Alshahrani, Mohammed S., Asonto, Laila Perlas, Tahan, Mohamed M. El, Sulaibikh, Amal H. Al, Sukayna Z. Al Faraj, Mulhim, Abdullah A. Al, Abbad, Murad F. Al, Nahhash, Samar A. Al, Moath N. Aldarweesh, Mahmoud, Alaa M., Nisreen Almaghraby, Jumaan, Mohammed A. Al, Thamir O. Al Junaid, Hawaj, Faisal M. Al, AlKenany, Samar, ElSayed, Omaima F., Abdelwahab, Haitham M., Moussa, Mohamed M., Bader K. Alossaimi, Shaikah K. Alotaibi, AlMutairi, Talal M., Duaa A. AlSulaiman, Shahrani, Saad D. Al, Alfaraj, Donia, Alhazzani, Waleed
SPIRIT checklist. (DOCX 45 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a47ea0f4e35ef7145b66309165f1dca6
Autor:
Alshahrani, Mohammed S., Asonto, Laila Perlas, Tahan, Mohamed M. El, Sulaibikh, Amal H. Al, Sukayna Z. Al Faraj, Mulhim, Abdullah A. Al, Abbad, Murad F. Al, Nahhash, Samar A. Al, Moath N. Aldarweesh, Mahmoud, Alaa M., Nisreen Almaghraby, Jumaan, Mohammed A. Al, Thamir O. Al Junaid, Hawaj, Faisal M. Al, AlKenany, Samar, ElSayed, Omaima F., Abdelwahab, Haitham M., Moussa, Mohamed M., Bader K. Alossaimi, Shaikah K. Alotaibi, AlMutairi, Talal M., Duaa A. AlSulaiman, Shahrani, Saad D. Al, Alfaraj, Donia, Alhazzani, Waleed
Ketamine for acute painful crisis in sickle cell disease patients—recognition pathway. (DOCX 115 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a35616476c2688da4fdb0de3aa9d707
Autor:
Alshahrani, Mohammed S., Asonto, Laila Perlas, Tahan, Mohamed M. El, Sulaibikh, Amal H. Al, Sukayna Z. Al Faraj, Mulhim, Abdullah A. Al, Abbad, Murad F. Al, Nahhash, Samar A. Al, Moath N. Aldarweesh, Mahmoud, Alaa M., Nisreen Almaghraby, Jumaan, Mohammed A. Al, Thamir O. Al Junaid, Hawaj, Faisal M. Al, AlKenany, Samar, ElSayed, Omaima F., Abdelwahab, Haitham M., Moussa, Mohamed M., Bader K. Alossaimi, Shaikah K. Alotaibi, AlMutairi, Talal M., Duaa A. AlSulaiman, Shahrani, Saad D. Al, Alfaraj, Donia, Alhazzani, Waleed
Ketamine for acute painful crisis in sickle cell disease—pain algorithm. (DOCX 176 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41c49ab9e2733aba7231e278f78781a9