Zobrazeno 1 - 10 of 20 pro vyhledávání: '"Faeza El-Dahtory"'
1
Akademický článek
Prevalence and patterns of chromosomal abnormalities among Egyptian patients with infertility: a single institution’s 5-year experience
Autor: Faeza El-Dahtory, Sohier Yahia, Rabab Ahmed Rasheed, Yahya Wahba
Publikováno v: Middle East Fertility Society Journal, Vol 27, Iss 1, Pp 1-5 (2022)
Abstract Background Chromosomal abnormalities represent an important cause of human infertility. Little is known about the prevalence of chromosomal abnormalities among Egyptian couples with infertility. We estimated the cytogenetic profiles and seme
Externí odkaz: https://doaj.org/article/7f558de29cf44c5b922df4ae885bcfbc
Zobrazit plný text záznamu
2
Akademický článek
Prevalence of iron deficiency anemia and beta thalassemia carriers among relatives of beta thalassemia patients in Nile Delta region, Egypt: a multicenter study
Autor: Mohamed R. El-Shanshory, Laila M. Sherief, Hoda M. Hassab, Seham M. Ragab, Sohier Yahia, Ahmed K. Mansour, Adel S. Ahmed, Said H. Abdou, Amal M. Helmy, Mona M. Watany, Ahmed M. Gad ALllah, Myriam A. Guindy, Zeinab I. Mourad, Mohamed A. Soliman, Reham M. El-Farahaty, Faeza El-Dahtory, Ahmad Darwish, Suzy Abd Elmabood, Ibrahim A. Kabbash, Shimaa M. Saied
Publikováno v: Journal of the Egyptian Public Health Association, Vol 96, Iss 1, Pp 1-8 (2021)
Abstract Background Screening of β thalassemia among close relatives is more feasible in highly prevalent countries with limited resources. The purpose of this study is to determine the prevalence of β thalassemia carriers and iron deficiency anemi
Externí odkaz: https://doaj.org/article/5ea6bca306f6434985317f4b2fc98a64
Zobrazit plný text záznamu
4
Prevalence of iron deficiency anemia and beta thalassemia carriers among relatives of beta thalassemia patients in Nile Delta region, Egypt: a multicenter study
Autor: Ahmed K Mansour, Suzy Abd Elmabood, Zeinab I. Mourad, Ahmad Darwish, Said Abdou, Seham M Ragab, Sohier Yahia, Mona Watany, Mohamed A Soliman, Reham M. El-farahaty, Shimaa M. Saied, Hoda Hassab, Laila M. Sherief, Myriam AbouSeif Guindy, Amal M. Helmy, Adel S. Ahmed, Mohamed El-Shanshory, Ahmed M. Gad ALllah, Ibrahim Kabbash, Faeza El-Dahtory
Publikováno v: Journal of the Egyptian Public Health Association
Journal of the Egyptian Public Health Association, Vol 96, Iss 1, Pp 1-8 (2021)
Background Screening of β thalassemia among close relatives is more feasible in highly prevalent countries with limited resources. The purpose of this study is to determine the prevalence of β thalassemia carriers and iron deficiency anemia among r
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::352948fb8a5f148dcee182fffc34970f
http://europepmc.org/articles/PMC8505559
Zobrazit plný text záznamu
5
Melatonin counteracts age-related progression of oxidative stress in young Down syndrome patients
Autor: Mohamed E. Abdraboh, Faeza El-Dahtory, Nissren Khafaga, Mohamed A. El missiry, Azza I. Othman
Publikováno v: Journal of Bioscience and Applied Research. 2:470-479
Melatonin (MLT) is a pineal gland hormone known for its potent antioxidant effect associated with neural protection. The presence of three copies of the SOD gene is considered to be the main cause of oxidative stress-dependent neural degeneration and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d4eff188fc1e9932e02f6e7bc370aa54
https://doi.org/10.21608/jbaar.2016.108736
Zobrazit plný text záznamu
6
The Progins Progesterone Receptor Gene Polymorphism and Polymorphism of the Estrogen Receptor β Gene in Endometriosis
Autor: Amal K. Seleem, Faeza el Dahtory, A. A. Abdel Aziz, Eatimad A. Basha, E. H. El. Sayd
Publikováno v: IOSR Journal of Pharmacy and Biological Sciences. 9:16-22
Objective: To determine the frequency of the PROGINS polymorphism and the estrogen receptor b gene (ERβ) +1730 G/A polymorphism in infertile women with endometriosis and fertile women. Subjects and methods: Case-control study included 50 women with
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::60c9cf50b90eda9d91b57861d048e434
https://doi.org/10.9790/3008-09311622
Zobrazit plný text záznamu
9
Chromosomal abnormalities as a cause of recurrent abortions in Egypt
Autor: Faeza El-Dahtory
Publikováno v: Indian Journal of Human Genetics
Background: In 4%-8% of couples with recurrent abortion, at least one of the partners has chromosomal abnormality. Most spontaneous miscarriages which happen in the first and second trimesters are caused by chromosomal abnormalities. These chromosoma
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf5b1a96efaede7c6ade9645270e687f
http://europepmc.org/articles/PMC3214323
Zobrazit plný text záznamu
10
Hidden Y Chromosome Mosaicism in 48 Egyptian Patients with Turner’s Syndrome
Autor: Sohier Yahia, Faeza El-Dahtory, El Hadidy M. El Hadidy, Sahar Hamed, Mervat M El-Eshmawy, Mohamed Ragab
Publikováno v: Genetics Research International
Genetics Research International, Vol 2013 (2013)
Background. The presence of Y chromosome material in Turner’s syndrome (TS) patients is a risk factor for the development of gonadoblastoma. Although conventional cytogenetic analysis is the definitive diagnosis of TS, low level Y chromosome mosaic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1974a63f4c84cfb3c127d4d0b04f06c7
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje