Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mohamad Abdel-Aziz"'
Autor:
Eslam Maamoun, mohamad abdel aziz
Publikováno v:
Iranian Journal of Medical Physics, Vol 17, Iss 5, Pp 298-302 (2020)
Introduction: The image quality of computed tomography (CT) can be seriously lowered by metal implants of patients. These implants are known to exert a significant impact on diagnostic accuracy due to artifacts. The current study aimed to assess the
Externí odkaz:
https://doaj.org/article/b57c8d0dcc0842bfb06dc777d05ca9eb
Publikováno v:
Pharmacological Reports. 74:570-582
The indole moiety is one of the most widespread heterocycles found in both natural products and biological systems. Indoles have important biological activities including anticancer, antioxidant, anti-inflammatory, antifungal, anticholinesterase, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bf50e3be4261bc3c3c2ed1cec4bd2ed
https://doi.org/10.1007/s43440-022-00370-3
https://doi.org/10.1007/s43440-022-00370-3
Publikováno v:
Canadian Journal of Civil Engineering. 32:1138-1151
Fiber reinforced polymer (FRP) tendons are being increasingly used nowadays in prestressing and (or) post-tensioning concrete structures. However, designers are faced with lack of practical analysis procedure that leads to proper evaluation of their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f119ff9fa31879c669c1a38b791c6905
https://doi.org/10.1139/l05-071
https://doi.org/10.1139/l05-071
Publikováno v:
Journal of Heterocyclic Chemistry. 42:943-946
Several new benzo[ij]pyrano[2,3-b]quinolizine-8-ones 5 and 4H-pyrano[2,3-b]pyridine 8 derivatives were synthesized from 4-hydroxyquinolines 1. Reacting 3-acetyl-4-hydroxy-1-phenyl-1H-quinoline-2-one with dimethylformamide dimethylacetal afforded 3-(3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfadc6a4dd5af21d8d45ef6d0b0dee64
https://doi.org/10.1002/jhet.5570420529
https://doi.org/10.1002/jhet.5570420529
Publikováno v:
ChemInform. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2e31e80702aba43c8edbe13ddee81be
https://doi.org/10.1002/chin.200547143
https://doi.org/10.1002/chin.200547143
Publikováno v:
Journal of Heterocyclic Chemistry; Jul2005, Vol. 42 Issue 5, p943-946, 4p
Publikováno v:
Journal of Heterocyclic Chemistry; July 2005, Vol. 42 Issue: 5 p943-946, 4p
Publikováno v:
ChemInform; Nov2005, Vol. 36 Issue 47, pno-no, 1p