Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ghada Mohamed Elhady"'
Sperm chromosomal abnormalities in infertile men with failed intracytoplasmic sperm injection (ICSI)
Autor:
Rania Fathy Elnahas, Amal Kotb Behery, Soha Kholeif, Yasser Ibrahim Orief, Ghada Mohamed Elhady
Publikováno v:
Middle East Fertility Society Journal, Vol 28, Iss 1, Pp 1-12 (2023)
Abstract Background Male infertility is a major health problem with multi-factorial etiology. Intracytoplasmic sperm injection (ICSI) has revolutionized the treatment of men with severely compromised semen parameters and improved their chances of ach
Externí odkaz:
https://doaj.org/article/913d91eff59a4e8eb89496e45c27741a
Publikováno v:
Journal of Human Reproductive Sciences, Vol 13, Iss 4, Pp 340-348 (2020)
Background: Recurrent pregnancy loss (RPL) is a major reproductive health issue, affecting 2%–5% of couples. Genetic factors, mainly chromosomal abnormalities, are the most common cause of early miscarriage accounting for 50%–60% of first trimest
Externí odkaz:
https://doaj.org/article/09503721e53241728a46364280c1efff
Autor:
Ghada Mohamed Elhady, Hanan Mahrous, Soha F. Kholeif, Emad El Din Khalifa, Dalia Mostafa Nayel
Publikováno v:
The Application of Clinical Genetics
Dalia Mostafa Nayel,1 Hanan Salah El Din Mahrous,1 Emad El Din Khalifa,2 Soha Kholeif,1 Ghada Mohamed Elhady1 1Department of Human Genetics, Medical Research Institute, Alexandria University, Alexandria, Egypt; 2Department of Obstetrics and Gynecolog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea214c4a237813ab8c8cb7aa007e97a7
https://doi.org/10.2147/tacg.s299349
https://doi.org/10.2147/tacg.s299349
Publikováno v:
Clinical Ophthalmology. 13:2217-2223
Purpose In the present study, we investigated whether interleukin 1 beta (IL1B) promoter polymorphisms are associated with keratoconus in an Egyptian population and their association with disease severity. Methods A total of 95 Egyptian keratoconus p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab5030672a50451fecf2c58a6769ce14
https://doi.org/10.2147/opth.s220723
https://doi.org/10.2147/opth.s220723
Autor:
Ebtesam M. Abdalla, Adrianna Mostowska, Agnieszka Gaczkowska, Karin Dowidar, Ghada Mohamed Elhady, Paweł P. Jagodziński
Publikováno v:
Archives of Oral Biology. 68:21-28
Objective Mutations in the EDA gene, encoding the epithelial morphogen ectodysplasin-A, can result in different but overlapping phenotypes. Therefore the aim of the study was to search for etiological variations of EDA and other candidate genes in tw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c1d09f55904d7762779badc38ecb3e2
https://doi.org/10.1016/j.archoralbio.2016.03.015
https://doi.org/10.1016/j.archoralbio.2016.03.015
Autor:
Morteza Seifi, Michael A. Walter, Tim Footz, Sherry Taylor, Ghada Mohamed Elhady, Ebtesam M. Abdalla
Publikováno v:
Acta Ophthalmologica. 94:e571-e579
Purpose Mutations in the bicoid-like transcription factor PITX2 gene often result in Axenfeld-Rieger syndrome (ARS), an autosomal-dominant inherited disorder. We report here the discovery and characterization of novel PITX2 deletions in a small kindr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5911af91fd15dd91a1a77e5afc8542c
https://doi.org/10.1111/aos.13030
https://doi.org/10.1111/aos.13030
Publikováno v:
Journal of Human Reproductive Sciences, Vol 13, Iss 4, Pp 340-348 (2020)
Journal of Human Reproductive Sciences
Journal of Human Reproductive Sciences
Background: Recurrent pregnancy loss (RPL) is a major reproductive health issue, affecting 2%–5% of couples. Genetic factors, mainly chromosomal abnormalities, are the most common cause of early miscarriage accounting for 50%–60% of first trimest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bebd4612cea601e915374ac08ba0e777
https://doi.org/10.4103/jhrs.jhrs_11_20
https://doi.org/10.4103/jhrs.jhrs_11_20
Publikováno v:
The Turkish Journal of Pediatrics. 61:780
Nazmy N, Elhady G, Refaat E, Kholeif S. Familial reciprocal non robertsonian translocation t(14;22) resulting in 22q11.2 deletion syndrome. Turk J Pediatr 2019; 61: 780-785. We report the clinical and genetic characterization of 2 cousins sharing the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::183127ff97d21ee9739f7d19fde0628a
https://doi.org/10.24953/turkjped.2019.05.020
https://doi.org/10.24953/turkjped.2019.05.020