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Page 1
Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype.
Al Tuwaijri A, Alyafee Y, Umair M, Alsubait A, Alharbi M, AlEidi H, Ballow M, Aldrees M, Alam Q, Al Abdulrahman A, Alrifai MT, Alfadhel M. Al Tuwaijri A, et al. Among authors: aldrees m. Mol Genet Genomic Med. 2023 Apr;11(4):e2117. doi: 10.1002/mgg3.2117. Epub 2022 Nov 24. Mol Genet Genomic Med. 2023. PMID: 36426412 Free PMC article.
Evolving sequence mutations in the Middle East Respiratory Syndrome Coronavirus (MERS-CoV).
AlBalwi MA, Khan A, AlDrees M, Gk U, Manie B, Arabi Y, Alabdulkareem I, AlJohani S, Alghoribi M, AlAskar A, AlAjlan A, Hajeer A. AlBalwi MA, et al. Among authors: aldrees m. J Infect Public Health. 2020 Oct;13(10):1544-1550. doi: 10.1016/j.jiph.2020.06.030. Epub 2020 Jul 1. J Infect Public Health. 2020. PMID: 32654959 Free PMC article.
Mutated VWA8 Is Associated With Developmental Delay, Microcephaly, and Scoliosis and Plays a Novel Role in Early Development and Skeletal Morphogenesis in Zebrafish.
Umair M, Farooq Khan M, Aldrees M, Nashabat M, Alhamoudi KM, Bilal M, Alyafee Y, Al Tuwaijri A, Aldarwish M, Al-Rumayyan A, Alkhalaf H, Wadaan MAM, Alfadhel M. Umair M, et al. Among authors: aldrees m. Front Cell Dev Biol. 2021 Oct 1;9:736960. doi: 10.3389/fcell.2021.736960. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34660594 Free PMC article.
Pancytopenia, Recurrent Infection, Poor Wound Healing, Heterotopia of the Brain Probably Associated with A Candidate Novel de Novo CDC42 Gene Defect: Expanding the Molecular and Phenotypic Spectrum.
Asiri A, Alwadaani D, Umair M, Alhamoudi KM, Almuhanna MH, Nasir A, Alrfaei BM, Al Tuwaijri A, Barhoumi T, Alyafee Y, Almuzzaini B, Aldrees M, Ballow M, Alayyar L, Al Abdulrahman A, Alhaidan Y, Al Ghasham N, Al-Ajaji S, Alsalamah M, Al Suwairi W, Alfadhel M. Asiri A, et al. Among authors: aldrees m. Genes (Basel). 2021 Feb 20;12(2):294. doi: 10.3390/genes12020294. Genes (Basel). 2021. PMID: 33672558 Free PMC article.
Multi-drug carbapenem-resistant Klebsiella pneumoniae infection carrying the OXA-48 gene and showing variations in outer membrane protein 36 causing an outbreak in a tertiary care hospital in Riyadh, Saudi Arabia.
Uz Zaman T, Aldrees M, Al Johani SM, Alrodayyan M, Aldughashem FA, Balkhy HH. Uz Zaman T, et al. Among authors: aldrees m. Int J Infect Dis. 2014 Nov;28:186-92. doi: 10.1016/j.ijid.2014.05.021. Epub 2014 Sep 19. Int J Infect Dis. 2014. PMID: 25245001 Free article.