Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Fatma, Elmougy"'
Publikováno v:
Pediatria Polska, Vol 97, Iss 2, Pp 89-94 (2022)
Externí odkaz:
https://doaj.org/article/c4af2719872c4fed8024146ae1a14dec
Autor:
Heba Asfour, Heba Baz, Hend Soliman, Yasmine Elshiwy, Marwa Elsharkawy, Fatma Elmougy, Marianne Morgan
Publikováno v:
Beni-Suef University Journal of Basic and Applied Sciences, Vol 10, Iss 1, Pp 1-7 (2021)
Abstract Background Measurement of multiple steroids, 17 hydroxyprogesterone, 11 deoxycortisol, and 21 deoxycortisol, is required to discriminate between congenital adrenal hyperplasia due to 21 hydroxylase deficiency and that due to 11 beta hydroxyl
Externí odkaz:
https://doaj.org/article/255039256b8941f493f7ac28dcca01ee
Autor:
Aisha Tolba, Iman Mandour, Noha Musa, Fatma Elmougy, Mona Hafez, Sahar Abdelatty, Amany Ibrahim, Hend Soliman, Bahaaeldin Labib, Yasmine Elshiwy, Tarek Ramzy, Marwa Elsharkawy
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Congenital adrenal hyperplasia (CAH) is a monogenic disorder caused by genetic diversity in the CYP21A2 gene, with 21-hydroxylase deficiency (21-OHD) as the most common type. Early sex assignment and early diagnosis of different genetic v
Externí odkaz:
https://doaj.org/article/d54fedd089d84afca5532e910449686d
Autor:
Dina Khedr, Mona Hafez, Jairo Lumpuy-Castillo, Soha Emam, Antoine Abdel-Massih, Fatma Elmougy, Rasha Elkaffas, Ignacio Mahillo-Fernández, Oscar Lorenzo, Noha Musa
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 14, p 5079 (2020)
Uncontrolled type-1 diabetes (T1DM) can lead to dyslipidaemia and albuminuria, which may promote cardiovascular injuries. However, some lipidemic factors could be useful in predicting cardiac dysfunction. Seventy-eight adolescents under insulin treat
Externí odkaz:
https://doaj.org/article/990504e55bb2495aa28609f83cdd8cc7
Autor:
Fatma, Elmougy, Sahar, Sharaf, Mona, Hafez, Ahmed, Khattab, Hazem, Abou-Yousef, Marwa, Elsharkawy, Heba, Baz, Sherif, Ekladious, Balsam, Sherif, Noha, Musa, Yasmin, Elshiwy, Alaa, Afif, Mona, Abdullatif, Ghada, Thabet, Normeen, Rady, Amany, Ibrahim, Hend, Soliman
Publikováno v:
Annals of the New York Academy of Sciences. 1415(1)
CYP21A2 genotyping remains an important element in the diagnosis and management of congenital adrenal hyperplasia, and establishing accurate genotype-phenotype correlations has facillitated adequate genetic counseling and prenatal management for at-r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9ad0e3166d53369a8e05159bba2fef4e
https://pubmed.ncbi.nlm.nih.gov/29266270
https://pubmed.ncbi.nlm.nih.gov/29266270