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A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational investigations.
Ammar M, Safi W, Tlili A, Alila-Fersi O, Frikha F, Chouchen J, Mnif F, Kharrat M, Maalej M, Felhi R, Abid M, Mnif-Feki M, Kacem FH, Fakhfakh F, Mkaouar-Rebai E. Ammar M, et al. Among authors: safi w. Int J Dev Neurosci. 2022 Nov;82(7):626-638. doi: 10.1002/jdn.10215. Epub 2022 Jul 25. Int J Dev Neurosci. 2022. PMID: 35841120
Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation.
Moalla M, Safi W, Babiker Mansour M, Hadj Kacem M, Mahfood M, Abid M, Kammoun T, Hachicha M, Mnif-Feki M, Hadj Kacem F, Hadj Kacem H. Moalla M, et al. Among authors: safi w. Front Endocrinol (Lausanne). 2021 Jul 29;12:684018. doi: 10.3389/fendo.2021.684018. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34393998 Free PMC article. Review.
Effect of COVID-19 Pandemic on Depression and Medications Use on Nursing Home Residents.
Dahab L, Dahab L, Abdelgadir K, Obeid T, Dey S, Ahmed M, Al-Safi W, Mohamed A, Lungba R, Abu Bakr A, Abdelrahman N. Dahab L, et al. Among authors: al safi w. J Am Med Dir Assoc. 2021 Mar;22(3):B20-B21. doi: 10.1016/j.jamda.2021.01.046. Epub 2021 Feb 24. J Am Med Dir Assoc. 2021. PMID: 34287166 Free PMC article. No abstract available.
Occurrence of Hypopituitarism in Tunisian Turner Syndrome patients: familial versus sporadic cases.
Mnif-Feki M, Safi W, Bougacha-Elleuch N, Abid G, Moalla M, Elleuch M, Ben Salah DH, Rekik N, Belguith N, Abdelhedi F, Kammoun T, Hachicha M, Charfi N, Mnif F, Kammoun H, Hadj Kacem H, Hadj-Kacem F, Abid M. Mnif-Feki M, et al. Among authors: safi w. Gynecol Endocrinol. 2021 Sep;37(9):848-852. doi: 10.1080/09513590.2021.1939298. Epub 2021 Jun 14. Gynecol Endocrinol. 2021. PMID: 34124982
31 results