Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Safa A. Faraj"'
Autor:
Ahmed I. Ansaf, Alaa M. Al-Rubae, Taghreed S. Saeed Al-Rawi, Sarah A. Najem, Hamasat J. Ali, Safa A. Faraj, Raid M. Al-Ani
Publikováno v:
Journal of Applied Hematology, Vol 15, Iss 2, Pp 116-120 (2024)
BACKGROUND: Despite prolonged life expectancy in patients with beta-thalassemia due to modern chelation therapy and planned blood transfusions, they still suffer from multisystem complications of this chronic hemolytic anemia, including endocrine sys
Externí odkaz:
https://doaj.org/article/66bc0ebee8bd4727ab80ec33b38b9dd0
Autor:
Safa A. Faraj
Publikováno v:
مجلة كلية الطب, Vol 58, Iss 2 (2016)
Background: Changes of coagulation profile have been described in patients with B-Thalassemia major. Prolongation of prothrombin time and partial thromboplastin time and reduced levels of coagulation factors and natural anticoagulants have been vario
Externí odkaz:
https://doaj.org/article/acc80fc66c2d4169989d72b2b924e187
Publikováno v:
Iraqi Journal of Hematology, Vol 9, Iss 2, Pp 118-122 (2020)
BACKGROUND: The onus of red blood cell transfusions in the pediatric emergency rooms (ERs) is paramount, with no specified guidelines, and almost all current policies are based on the obtainable adult facts. OBJECTIVES: The aims were to study the cur
Externí odkaz:
https://doaj.org/article/6b7f1232a7cc437da23e832d9ca31432
Autor:
Lika’a Fasih Y. Al-Kzayer, Raghad M. Saeed, Hasanein Habeeb Ghali, Miyuki Tanaka, Mazin F. Al-Jadiry, Safa A. Faraj, Salma A. Al-Hadad, Hussam M. Salih Al Abdullah, Athar A. Majeed, Ali Omer Qadir, Dana Ahmed Abdullah, Kani Dlawar Noori, Zheyan Mohammed Hama, Abdulrahman A. Muhsin, Adnan Anwer Al-Doski, Yasir S. Al-Agele, Abduladheem H. Malallah, Khalid S. Al-Badrani, Asmaa M. A. Khaleel, Minoru Kamata, Motoharu Hamada, Seiji Kojima, Yozo Nakazawa, Yusuke Okuno
Publikováno v:
Translational Pediatrics. 12:827-844
Autor:
Safa A. Faraj, Naeem M. Al-Abedy
Publikováno v:
Iron Metabolism-A Double-Edged Sword
The hepcidin is antimicrobial peptide has antimicrobial effects discover before more than a thousand years; it has a great role in iron metabolism and innate immunity. Hepcidin is a regulator of iron homeostasis. Its production is increased by iron e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d9b2bf57ce783bbb2eeeb888aaa9013
https://mts.intechopen.com/articles/show/title/hepcidin
https://mts.intechopen.com/articles/show/title/hepcidin
Publikováno v:
International Journal of Research in Pharmaceutical Sciences. 12:676-682
Thalassemia is an inherited disorder causing an imbalance in the development of the globin chain with ineffective erythropoiesis and increased peripheral consumption. Expansion of bone marrow decreases bone mineral density. Bone disease in thalassemi
Publikováno v:
Genetic Variation
This chapter sheds light on hepcidin, historical view of hepcidin, and the time of its discovery in the first section. Then this chapter gives information about the genetic aspect and the importance of gene knowledge of hepcidin in explaining many di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::019f4f8142e13d1e133576f997dcf574
http://www.intechopen.com/articles/show/title/serum-hepcidin-hormone-level-and-its-genes-polymorphism
http://www.intechopen.com/articles/show/title/serum-hepcidin-hormone-level-and-its-genes-polymorphism
Publikováno v:
Indian Journal of Forensic Medicine & Toxicology.
Publikováno v:
Annals of Tropical Medicine and Public Health. 22:158-170
Publikováno v:
Medico-Legal Update.
Case control study was used,with Glanzmann’s thrombasthenia (GT) patients (n=15) and healthy individualcontrol (n=20).It was successfully identified three SNP in ITGB3 gene by using PCR technique and direct sequencing . Thefirst SNP c. * 1479T> C (