Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Heba H. Abou-Elew"'
Publikováno v:
Annals of Saudi Medicine, Vol 32, Iss 2, Pp 200-202 (2012)
BACKGROUND AND OBJECTIVE: The risk of blood-borne infections, especially hepatitis C virus (HCV) and human immunodeficiency virus (HIV) infection still remains in developing countries among children receiving blood products as hemophiliacs, but the r
Externí odkaz:
https://doaj.org/article/c9afb4be987c4afc9b716e7a5e0d2dac
Autor:
Ilham Youssry, Nevine Fouad, Heba H Abou-Elew, Shireen Hefny, Rania H. Hashem, Rania A. Zayed
Publikováno v:
Hematology. 23:362-367
Background and aim of work: Sickle cell disease (SCD) is an inherited disease of the beta globin gene. The βS globin gene haplotypes are Senegal, Benin, Bantu, Cameroon, Arab-Indian and atypical haplotypes. In SCD, stroke is a life-threatening event
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9aa65cd2f4fbfd2d242668290863ed32
https://doi.org/10.1080/10245332.2017.1403736
https://doi.org/10.1080/10245332.2017.1403736
Autor:
Heba H, Abou-Elew, Ilham, Youssry, Shireen, Hefny, Rania H, Hashem, Nevine, Fouad, Rania A, Zayed
Publikováno v:
Hematology (Amsterdam, Netherlands). 23(6)
Sickle cell disease (SCD) is an inherited disease of the beta globin gene. The βFifty-two SCD patients were included in the study, they were 26 males and 26 females with age range from 3 to 18 years old. The PCR-RFLP technique was used for the deter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c7247ab71634c77279f882955423bcdb
https://pubmed.ncbi.nlm.nih.gov/29157167
https://pubmed.ncbi.nlm.nih.gov/29157167
Publikováno v:
Annals of clinical and laboratory science. 44(3)
Mutations of the HAMP gene and HFE gene have a role in iron overload. We assessed the frequency of the G71D mutation of the HAMP gene and the H63D mutation of the HFE gene and the correlation between these mutations as well as the correlation between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6032febea31edb4c7670c1a8bb2bfc43
https://pubmed.ncbi.nlm.nih.gov/25117103
https://pubmed.ncbi.nlm.nih.gov/25117103
Autor:
Rania Hammoud, Hanaa H. Arnaout, Hanan Ahmed, Doha A. Mokhtar, Hanan Raslan, Heba H Abou-Elew, Magy Abdelwahab
Publikováno v:
Annals of hematology. 90(5)
Hemophilia A (HA) is the most common severe bleeding disorder in humans, affecting one in 5,000 male births. In severe HA, intron 22 inversion of F8 is the most prevalent mutation, accounting for 40–50% of all mutations; however, little is known ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a281ec50c3537f7e24334d15b56f9cc8
https://pubmed.ncbi.nlm.nih.gov/21072517
https://pubmed.ncbi.nlm.nih.gov/21072517
Autor:
Heba H Abou-Elew, Doha A. Mokhtar, Amira Edris, Ilham Youssry, Lobna El Messery, Naglaa Tawfik, Samia Rizk
Publikováno v:
Pediatrics. 121:S124-S124
INTRODUCTION: For neonatal sepsis, several clinical and laboratory parameters have been proposed for its diagnosis but with variable sensitivity and specificity. The bacterial products in sepsis, including endotoxin, induce the production of proinfla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efb9a2c780d38a296a3d31e22a5eac7f
https://doi.org/10.1542/peds.2007-2022cccc
https://doi.org/10.1542/peds.2007-2022cccc
Autor:
Abou-Elew H; Clinical and Chemical Pathology Department, New Children Hospital, Faculty of Medicine, Cairo University, Cairo, Egypt. heb_rahman@lycos.com, Ahmed H, Raslan H, Abdelwahab M, Hammoud R, Mokhtar D, Arnaout H
Publikováno v:
Annals of hematology [Ann Hematol] 2011 May; Vol. 90 (5), pp. 579-84. Date of Electronic Publication: 2010 Nov 12.