Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Shaikha Al Arrayed"'
Autor:
Shaikha Al Arrayed, Amani Al Hajeri
Publikováno v:
Advances in Hematology, Vol 2012 (2012)
Introduction. The incidence of genetic blood disease in Bahrain has declined gradually since 1984 when the Ministry of Health (MOH) instituted a prevention campaign. The national NBS program for hemoglobinopathies was started in May 2007, financed by
Externí odkaz:
https://doaj.org/article/66877b89ee8f4a83b6592a6fd5f46b83
Autor:
Al Alawi Ahmed, Thabet Ahmed, Nabeel J. Al Moamen, Hassan Sanad, Shaikha Al Arrayed, Ruqaya Abbas, Fawzia Mahdi, Ebtihal Salman
Publikováno v:
Hemoglobin. 37:369-377
Silent β-thalassemia (β-thal) is a group of mutations affecting the β-globin gene that cannot be differentiated in heterozygote states from normal conditions by using conventional criteria for the diagnosis of β-thal trait. Here we report the exi
Autor:
Shaikha Al Arrayed, Amani Al Hajeri
Publikováno v:
Annals of Saudi Medicine, Vol 30, Iss 4, Pp 284-288 (2010)
Annals of Saudi Medicine
Annals of Saudi Medicine
Background and Objectives : Previous studies that have assessed patient awareness of the management of sickle cell disease (SCD) indicated a lack of awareness of the disease and possibly a need for more public education. Therefore, we measured public
Autor:
Hanan Hamamy, Shaikha Al-Arrayed
Publikováno v:
Journal of biosocial science. 44(3)
SummaryConsanguineous marriage is traditional and respected in most communities of North Africa, the Middle East and West Asia, including Bahrain, with intra-familial unions accounting for 20–50+% of all marriages. Significant secular changes in co
Autor:
Shaikha Al-Arrayed
Publikováno v:
Bahrain Medical Bulletin. 35:55-55