Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Alaa Masoud Abd El Gayed"'
Publikováno v:
Bulletin of Egyptian Society for Physiological Sciences. 38:13-26
Background: Polycystic ovary syndrome (PCOS) is one of the commonest endocrine disorder affecting the women in childbearing period. Accumulating evidences from recent studies indicate that vitamin D receptor (VDR)Taq1(Tt) genetic variants may contrib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a541654a42460a67056f139801425c13
https://doi.org/10.21608/besps.2018.8099
https://doi.org/10.21608/besps.2018.8099
Autor:
Aziza Mahmoud Mohamed Zaki, Eman Masoud Abd El Gayed, Alaa Masoud Abd El Gayed, Eman Abd-allah Mahmoud Fouda, Ibrahim Fathi Zaid
Publikováno v:
Gene Reports. 25:101327
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af655b5430decca864ed8ab8d06a58be
https://doi.org/10.1016/j.genrep.2021.101327
https://doi.org/10.1016/j.genrep.2021.101327
Autor:
Aziza Mahmoud Mohamed Zaki, Alaa Masoud Abd El Gayed, Ibrahim Fathi Zaid, Eman Abd-allah Mahmoud Fouda, Eman Masoud Abd El Gayed
Publikováno v:
Gene Reports. 24:101257
Background Preeclampsia (PE) is a familiar gestational complication that affects 3% to 5% of pregnant women. After 20 weeks of pregnancy, PE typically presents as new-onset hypertension and proteinuria. Inadequate trophoblast invasion, accompanied by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac521084618ed810bb2bec51359fbc39
https://doi.org/10.1016/j.genrep.2021.101257
https://doi.org/10.1016/j.genrep.2021.101257
Publikováno v:
Meta Gene. 24:100649
A Preeclampsia (PE) is the commonest dangerous disorder during pregnancy and preeclampsia is characterized by increased level of (epinephrine and nor epinephrine). Renalase is an enzyme that cause break down of catecholamines, that leads to elevation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf7204ed4a6b4ba83eb91228ff5eab5a
https://doi.org/10.1016/j.mgene.2020.100649
https://doi.org/10.1016/j.mgene.2020.100649
Publikováno v:
Meta Gene. 23:100638
Polycystic ovary syndrome (PCOS) is a common endocrine disorder that affects approximately one in 15 females worldwide. A functional polymorphism of the 11-beta-hydroxysteroid dehydrogenase type 1 (HSD11B1) gene has been demonstrated to have a relati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67c38cbcca95cadb9e07fa18548c75df
https://doi.org/10.1016/j.mgene.2019.100638
https://doi.org/10.1016/j.mgene.2019.100638
Publikováno v:
Menoufia Medical Journal. 28:233
Objectives This study aimed to detect the relation between fasting C-peptide level and serum insulin level in pre-eclamptic pregnant women. Background Pre-eclampsia is a systemic disease that is characterized by increased vascular resistance, endothe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d450e3d87986e9be8f5b8c19a6939445
https://doi.org/10.4103/1110-2098.156000
https://doi.org/10.4103/1110-2098.156000
Publikováno v:
Menoufia Medical Journal. 28:873
Objective This study aimed to correlate lower uterine segment (LUS) thickness measured by both transvaginal (TVS) and transabdominal ultrasonography (TAS) after completion of 36 weeks of pregnancy with that measured manually using a caliper at the ti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cabb77882f7268eaaa967e3abcb58759
https://doi.org/10.4103/1110-2098.173606
https://doi.org/10.4103/1110-2098.173606
Publikováno v:
Menoufia Medical Journal. 28:245
Objective The aim of the study was to estimate the value of the nuchal translucency (NT) measurement during the period from 10th to 14th week of gestation in predicting the possibility of congenital malformation in these fetuses. Background First-tri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffef04269e11ce2f943b24192ada209f
https://doi.org/10.4103/1110-2098.156002
https://doi.org/10.4103/1110-2098.156002