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Archiv Der Pharmazie|April 10, 2010
Novel thiophenes, thienopyrimidines, and triazolothienopyrimidines for the evaluation of anticancer and augmentation effects of gamma-radiationMohamed A Shaaban, Mostafa M Ghorab, Helmy I Heiba, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|October 20, 2017
Randomized controlled trial of the effect of endometrial injury on implantation and clinical pregnancy rates during the first ICSI cycleAhmed M Maged, Hamsa Rashwan, Suzy AbdelAziz, et al.
Journal of Immunoassay & Immunochemistry|July 22, 2021
Interleukin19 gene polymorphism and its serum level in acne vulgaris patientsHeba Bazid, Alaa Marae, Nermin Tayel, et al.
Clinical Dysmorphology|March 15, 2006
3-M syndrome: a report of three Egyptian cases with review of the literatureSamia A Temtamy, Mona S Aglan, Adel M Ashour, et al.
Archives of Oral Biology|July 30, 2024
A novel missense variant in CAT gene causing acatalasemia with gangrenous periodontitis (Takahara's disease)Nehal F Hassib, Mennat Mehrez, Maha R Abouzaid, et al.
Journal of Pediatric Genetics|November 6, 2019
Early Detection and Management of Prader-Willi Syndrome in Egyptian PatientsHala T El-Bassyouni, Nagwa Hassan, Inas Mahfouz, et al.
Bioinorganic Chemistry and Applications|July 31, 2010
Antineoplastic Activity of New Transition Metal Complexes of 6-Methylpyridine-2-carbaldehyde-N(4)-ethylthiosemicarbazone: X-Ray Crystal Structures of [VO(2)(mpETSC)] and [Pt(mpETSC)Cl]Shadia A Elsayed, Ahmed M El-Hendawy, Sahar I Mostafa, et al.
International Journal of Dermatology|July 6, 2022
Study of purine derivatives and their relation to renal disorders in patients with psoriasisHeba A S Bazid, Mohamed A Shoeib, Samar El-Sayed, et al.
Journal of Immunoassay & Immunochemistry|March 15, 2023
Assessment of cytochrome P450 1A1 gene polymorphism and vitamin A serum level in psoriasis vulgarisHeba A S Bazid, Alaa Marae, Nermin Tayel, et al.
European Journal of Medical Genetics|August 25, 2020
Two new families with enamel renal syndrome: A novel FAM20A gene mutation and review of literatureNehal F Hassib, Mona A Shoeib, Hoda A ElSadek, et al.
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