Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Amani Al Hajeri"'
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:
Amani Al Hajeri
Publikováno v:
Journal of the Bahrain Medical Society. 29:41-47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5040c476aa20c3812d976cd4b74e3cf
https://doi.org/10.26715/jbms.29.3.2017.46a
https://doi.org/10.26715/jbms.29.3.2017.46a
Publikováno v:
Cochrane Database Syst Rev
The Cochrane Library
The Cochrane Library
Background Sickle cell disease is one of the most common genetic disorders. Sickle cell crises in which irregular and dehydrated cells contribute to blocking of blood vessels are characterised by episodes of pain. Treatment is mainly supportive and s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74cb68e22180c970a4e615c115434916
https://pubmed.ncbi.nlm.nih.gov/17443614
https://pubmed.ncbi.nlm.nih.gov/17443614
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49924abca7009044a2b10ee2cb0ead43
https://doi.org/10.4103/0256-4947.65256
https://doi.org/10.4103/0256-4947.65256
Publikováno v:
Cochrane Database Syst Rev
The Cochrane Library
The Cochrane Library
Background Thalassaemia is an autosomal recessive blood disorder, caused by mutations in globin genes or their regulatory regions, resulting in a reduced rate of synthesis of one of the globin chains that make up haemoglobin. In β-thalassaemia there
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2298cf11d6b664d38f462c060df84c61
https://doi.org/10.1002/14651858.cd008708.pub3
https://doi.org/10.1002/14651858.cd008708.pub3
Publikováno v:
Annals of Saudi Medicine. 26:49-51
t is increasingly recognized that health care decision-making around the world needs to be informed by high quality and timely research evidence. The randomized controlled trial (RCT) has long been considered the “gold standard” in the hierarchy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c4dbbf1a2b432f7dbbf5de3078a7167
https://doi.org/10.5144/0256-4947.2006.49
https://doi.org/10.5144/0256-4947.2006.49
Publikováno v:
The Cochrane database of systematic reviews. (10)
Thalassemia is an inherited blood disorder, caused by mutations in regulatory genes and transmitted as an autosomal recessive disorder, which results in a reduced rate of synthesis of one of the globin chains that make up haemoglobin. In ß-thalassae
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a5ad3a7fadc118effe8e15e1835bb16a
https://pubmed.ncbi.nlm.nih.gov/25316103
https://pubmed.ncbi.nlm.nih.gov/25316103
Publikováno v:
The Cochrane Library
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e543fb3587520bb40e9c2afea183c7ea
https://doi.org/10.1002/14651858.cd008708
https://doi.org/10.1002/14651858.cd008708