Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Salma Abdallah"'
Autor:
Osama M. Sarhan, Ahmed Al Farhan, Salma Abdallah, Hamzah Al Ghwanmah, Deena Boqari, Helmy Omar, Abdulmohsin Al Faddagh, Hanan Al Kanani, Fouad Al Kawai
Publikováno v:
Surgical Case Reports, Vol 8, Iss 1, Pp 1-5 (2022)
Abstract Background Metanephric adenoma (MA) is a rare benign renal tumor that resembles renal cell carcinoma and Wilms’ tumor in radiological as well as pathological appearance. It can present at any age or gender, and it is extremely rare in the
Externí odkaz:
https://doaj.org/article/512f9315fb864bf5bc316d538fda9c0f
Publikováno v:
Journal of Advanced Pharmacy Research. 7:111-119
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f41c713fccf5c4fd12af9f8c04a7602
https://doi.org/10.21608/aprh.2023.177396.1202
https://doi.org/10.21608/aprh.2023.177396.1202
Autor:
null Abdalla Eltoum Ali, null Sitana Alkhwad Hassan Mohamed, null Salma Abdallah Ali, null Salih A Elmahdi
Publikováno v:
International Journal of Biological and Pharmaceutical Sciences Archive. 4:013-024
Background: Atorvastatin is a lipid-lowering medication that causes skeletal muscle side effects by altering serum levels of skeletal muscle biomarkers. The aim of this study is to assess the effect of atorvastatin on muscle function and biomarker se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fcad9d2a0c079f6e8d10c66dc494413
https://doi.org/10.53771/ijbpsa.2022.4.2.0081
https://doi.org/10.53771/ijbpsa.2022.4.2.0081
Autor:
SALMA, ABDALLAH JAMEEL ABU1 abdullah.abusalma@aau.ac.ae, PRASOLOV, VALERIY2, GLAZKOVA, IRINA3 glazkovair3@rambler.ru, ROGULIN, RODION4
Publikováno v:
Montenegrin Journal of Economics. Sep2021, Vol. 17 Issue 3, p131-143. 13p.
Publikováno v:
Blood Coagulation & Fibrinolysis. 30:277-280
Rare clotting factor (F) deficiency is a deficiency of one or more of coagulation factors other than FVIII, FIX and vonWillebrand (FI, FII, FV, FV + FVIII, FVII, FIX, FX, FXI and FXIII) that cause bleeding disorders and are inherited as autosomal rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d86976ee01db421c80f8d0bd37c6f76
https://doi.org/10.1097/mbc.0000000000000834
https://doi.org/10.1097/mbc.0000000000000834