Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Abdullah Al Enazi"'
Publikováno v:
Journal of Applied Hematology, Vol 11, Iss 3, Pp 132-134 (2020)
Leukocyte adhesion deficiency type II (LAD II) is a rare hereditary disorder caused by the mutation in the guanosine diphosphate-fucose transporter gene (SLC35C1). LAD II is characterized by inexpression of ABO antigens (i.e., Bombay phenotype) and t
Externí odkaz:
https://doaj.org/article/2d7f26ecbe5a410780e852360f0b066b
Publikováno v:
Journal of Applied Hematology, Vol 11, Iss 3, Pp 132-134 (2020)
Leukocyte adhesion deficiency type II (LAD II) is a rare hereditary disorder caused by the mutation in the guanosine diphosphate-fucose transporter gene (SLC35C1). LAD II is characterized by inexpression of ABO antigens (i.e., Bombay phenotype) and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::188230b98ffb81e03cbe4f0d1e26f8ef
http://www.jahjournal.org/article.asp?issn=1658-5127
http://www.jahjournal.org/article.asp?issn=1658-5127
Autor:
Bader Al Shabrain, Ahmed Mohammed Saleh Alduais, Abdullah Al Enazi, Salah Ghalib Mogali, Fuad Al-awad
Publikováno v:
IOSR Journal of Nursing and Health Science. 3:72-85
Purpose: The aim of this study was to find out the barriers preventing staff from reporting medical errors and identifying the strategies which might encourage the staff reporting the medical errors at Riyadh, Saudi Arabia. Method: The data was colle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0c6c3465c9da49caeae4e9ac0698eaa
https://doi.org/10.9790/1959-03537285
https://doi.org/10.9790/1959-03537285