Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Maha Moustafa"'
Autor:
Alaa Eldin M.A. Morshdy, Ahmed E. Tharwat, Hassan Maarouf, Maha Moustafa, Wageh S. Darwish, Waleed R. El-Ghareeb, Abdullah F. Alsayeqh, Nafissa A. Mustafa
Publikováno v:
Open Veterinary Journal, Vol 13, Iss 12, Pp 1738-1743 (2023)
Background: In Egypt, salted fish is considered a typical processed fish, including salted sardine, salted mullet (feseikh), keeled mullet (sahlia), and herrings. High-quality protein, polyunsaturated fatty acids, vital amino acids, and trace mineral
Externí odkaz:
https://doaj.org/article/9dc040832de54e80bf55aee51d968828
Autor:
Ibrahim H. Borai, Yehia Mohamed Shaker, Maha Moustafa Kamal, Wafaa M. Ezzat, Esmat Ashour, Mie Afify, Weaam Gouda, Maha M. Elbrashy
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 19, Iss 3, Pp 241-246 (2018)
Background and aims: Nonalcoholic fatty liver disease (NAFLD) is a complicated disease linked with dietary habitats, obesity, and a range of comorbidities correlated with insulin resistance.Although environmental parameters are essential in deciding
Externí odkaz:
https://doaj.org/article/1141661868744935a5967891e5938188
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 17, Iss 2, Pp 217-221 (2016)
Background: Polymorphisms of genes encoding enzymes involved in folate metabolism have long been hypothesized to be maternal risk factors for Down syndrome, however, results are conflicting and inconclusive. Aim of the study: To analyze the effect of
Externí odkaz:
https://doaj.org/article/978b4254910c49e2af55e3955bbd6f75
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 16, Iss 3, Pp 233-237 (2015)
Background: Paraoxonase (PON1) is an A-esterase capable of hydrolyzing the active metabolites (oxons) of many organophosphorus (OP) insecticides. Human PON1 displays two polymorphisms in the coding region (Q192R and L55M) and several polymorphisms in
Externí odkaz:
https://doaj.org/article/ef21d178da0442ee8799dfe29edd8813
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 15, Iss 4, Pp 355-360 (2014)
Introduction: Alzheimer’s disease (AD) is a progressive, neurodegenerative disease. Many studies proposed an association of the insertion (I)/deletion (D) polymorphism (indel) in intron 16 of the gene for angiotensin I-converting enzyme (ACE) on ch
Externí odkaz:
https://doaj.org/article/9b6835e228894e2ea04ea81097dfa6a6
Publikováno v:
Journal of Product & Brand Management, 2018, Vol. 27, Issue 7, pp. 832-846.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/JPBM-10-2017-1625
Autor:
Maha Moustafa
Publikováno v:
Transcultural Journal of Humanities and Social Sciences. 4:168-177
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78789cae954da6f61718bafe366224ad
https://doi.org/10.21608/tjhss.2023.292560
https://doi.org/10.21608/tjhss.2023.292560
Autor:
Ahmed, Maha Moustafa1 Maha.moustafa@women.asu.edu.eg, Mady, Heba Yehia1, El Namaky, Amira Hassan2
Publikováno v:
Polish Journal of Entomology. 2021, Vol. 90 Issue 4, p175-193. 19p.
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Publikováno v:
In Egyptian Journal of Medical Human Genetics July 2015 16(3):233-237