Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Faisal O. Al-Qurashi"'
Autor:
Elham A Hasan, Mohammad A Al Ghamdi, Amal A Algamdi, Bassam H. Awary, Dalal K. Bubshait, Faisal O. Al-Qurashi, Talal A Bou Shahmah, Mohammed Alshahrani, Waleed H Albuali, Mohammad H. Al-Qahtani, Abdullah A Yousef
Publikováno v:
Journal of Multidisciplinary Healthcare. 13:1507-1516
Purpose Currently, several scoring systems for predicting mortality in severely ill children who require treatment in a pediatric intensive care unit (PICU) have been established. However, despite providing high-quality care, children might develop c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1544470b7030af6dcd0831a0ae1a0b3
https://doi.org/10.2147/jmdh.s282108
https://doi.org/10.2147/jmdh.s282108
Autor:
Syed Husain, Omair Sharif, Bassam H. Awary, Faisal O. Al-Qurashi, Mohammad H. Al-Qahtani, Waleed H. Albuali, Abdullah A Yousef
Background: The Objective Structured Clinical Examination (OSCE) is a standard academic assessment tool in the field of medical education. This study aimed to present an innovative method for digitizing a computerized web-based Objective Structured C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8edc29f1c012ba377c6778581ef21deb
https://doi.org/10.21203/rs.3.rs-143684/v1
https://doi.org/10.21203/rs.3.rs-143684/v1
Publikováno v:
Saudi Journal of Medicine and Medical Sciences, Vol 5, Iss 1, Pp 67-70 (2017)
Saudi Journal of Medicine & Medical Sciences
Saudi Journal of Medicine & Medical Sciences
Omphalocele, exstrophy of the bladder, imperforate anus and spinal defect (OEIS) complex is a rare congenital multisystemic malformation representing unique anomalies. It was first reported in 1978 through a series of cases with an abnormality of bod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1536edeec4a4f1b0bbc3b1053ba6dbc2
http://www.sjmms.net/article.asp?issn=1658-631X
http://www.sjmms.net/article.asp?issn=1658-631X
Publikováno v:
Saudi Journal of Medicine and Medical Sciences, Vol 5, Iss 2, Pp 177-180 (2017)
Saudi Journal of Medicine & Medical Sciences
Saudi Journal of Medicine & Medical Sciences
Evans syndrome (ES) is a rare autoimmune disorder characterized by autoimmune hemolytic anemia (AIHA) and immune thrombocytopenic purpura (ITP). We report a case of a 4-month old infant who presented with a history of acute pallor and jaundice. She h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ab367cc07e7a56b3ef6e7b95aa694d8
http://www.sjmms.net/article.asp?issn=1658-631X
http://www.sjmms.net/article.asp?issn=1658-631X
Publikováno v:
Saudi Medical Journal
Saudi Medical Journal, Vol 37, Iss 4, Pp 414-419 (2016)
Saudi Medical Journal, Vol 37, Iss 4, Pp 414-419 (2016)
Objectives: To assess the epidemiological characteristics of prematurity and survival rate in preterm infants diagnosed at a university hospital in the Eastern province of Saudi Arabia. Methods: A retrospective study was carried out of 476 preterm in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9bebc435c36f6046f71328c557c6be8
https://doi.org/10.15537/smj.2016.4.14309
https://doi.org/10.15537/smj.2016.4.14309
Autor:
Saleh M. Alzahrani, Hussam Mohammad Abdullatif Abouollo, Abdullah A Yousef, Abdullah S Aljoudi, Nasser Y. Al-Jawder, Abdulrahman K. Al-Ahmar, Mosab S. Al-Majed, Faisal O. Al-Qurashi
Publikováno v:
ResearcherID
Objective The aim of this study was to evaluate the nonfatal drowning experience, risk factors, intrahospital assessment and postincidental outcomes for children admitted to King Fahd Hospital of the University, AlKhobar, Saudi Arabia, over a 10-year
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd537ed39328ffed370965ae23a3815f
http://journals.lww.com/pec-online/Fulltext/publishahead/A_Review_of_Nonfatal_Drowning_in_the_Pediatric_Age.98637.aspx
http://journals.lww.com/pec-online/Fulltext/publishahead/A_Review_of_Nonfatal_Drowning_in_the_Pediatric_Age.98637.aspx