Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Mohamed El-Awady"'
Publikováno v:
Egyptian Journal of Ear, Nose, Throat and Allied Sciences. 24:1-7
Publikováno v:
Delta University Scientific Journal. 5:76-107
Publikováno v:
Journal of Fluorescence. 32:1941-1948
We hereby introduce a sensitive fast straightforward spectrofluorometric method for the estimation of remdesivir and favipiravir. The two drugs are prescribed in some regimens to treat COVID‐19 pandemic disease, which is caused by SARS‐CoV‐2. T
Autor:
Maha, Wahdan, Sally, Hakim, Maha, El Gaafary, Dalia, Sos, Ghada, Wassif, Wafaa, Hussein, Amany, Mokhtar, Amr, Hussein, Mohamed, El Awady, Mervat, Rady, Wagida, Anwar
Publikováno v:
Eastern Mediterranean Health Journal. 28:336-344
Caesarean section (CS) is a life-saving operation when vaginal delivery is risky to the mother or baby. However, if not medically indicated or performed under suboptimal conditions, it can be harmful and resource-intensive.To estimate the prevalence
Autor:
mohamed El awady
Publikováno v:
Egyptian Journal of Ear, Nose, Throat and Allied Sciences. 23:1-6
Autor:
mohamed El awady, mohamed Ali
Publikováno v:
Egyptian Journal of Ear, Nose, Throat and Allied Sciences. 23:1-6
Publikováno v:
Egyptian Academic Journal of Biological Sciences, G. Microbiology. 13:79-90
Publikováno v:
Al-Azhar International Medical Journal.
Publikováno v:
Azhar International Journal of Pharmaceutical and Medical Sciences. 1:92-101
Validated, accurate, simple and reliable spectrophotometric method was described for the assay of dipyridamole and lamivudine in their different dosage forms. The suggested method depended on a binary reddish orange coloured complexformation between
Autor:
Nivine A. Helmy, Mervat Rady, Alaa K. Kamel, Mohamed El-Awady, Mona O. El Ruby, Mona K. Mekkawy, Khaled M Refaat, Ola M. Eid, Amal M. Mohamed, Engy A. Ashaat
Publikováno v:
Molecular Syndromology. 12:87-95
Mowat-Wilson syndrome (MWS) is a rare autosomal dominant syndrome characterized by dysmorphic features, mental retardation, and congenital heart disease (CHD). MWS results from microdeletions of chromosome 2q23 or de novo SNVs involving the ZEB2 gene