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Page 1
Gene therapy for spinal muscular atrophy: the Qatari experience.
Ali HG, Ibrahim K, Elsaid MF, Mohamed RB, Abeidah MIA, Al Rawwas AO, Elshafey K, Almulla H, El-Akouri K, Almulla M, Othman A, Musa S, Al-Mesaifri F, Ali R, Shahbeck N, Al-Mureikhi M, Alsulaiman R, Alkaabi S, Ben-Omran T. Ali HG, et al. Among authors: mohamed rb. Gene Ther. 2021 Nov;28(10-11):676-680. doi: 10.1038/s41434-021-00273-7. Epub 2021 Jul 19. Gene Ther. 2021. PMID: 34276047 Free PMC article.
Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients' cohort from Qatar. A population specific founder variant.
Abdel Aleem A, Elsaid MF, Chalhoub N, Chakroun A, Mohamed KAS, AlShami R, Kuzu O, Mohamed RB, Ibrahim K, AlMudheki N, Osman O, Ross ME, ELalamy O. Abdel Aleem A, et al. Among authors: mohamed rb. Neuromuscul Disord. 2020 Jun;30(6):457-471. doi: 10.1016/j.nmd.2020.03.009. Epub 2020 Apr 17. Neuromuscul Disord. 2020. PMID: 32444167
Permanent cutaneous vesicostomy: a pragmatic approach to safely manage lower urinary tract dysfunction in pediatric patients with chronic and life-limiting conditions and neuropathic bladders.
Vallasciani S, Al Saeedi A, Khalil IA, Mohamed RB, Muneer E, Abdelmaguid N, Pippi Salle JL. Vallasciani S, et al. Among authors: mohamed rb. Front Pediatr. 2024 Jun 25;12:1409608. doi: 10.3389/fped.2024.1409608. eCollection 2024. Front Pediatr. 2024. PMID: 38983461 Free PMC article.
Identification of strain diversity and phylogenetic analysis based on two major essential proteins of Orf viruses isolated from several clinical cases reported in Malaysia.
Bala JA, Balakrishnan KN, Jesse FFA, Abdullah AA, Noorzahari MSB, Ghazali MT, Mohamed RB, Haron AW, Noordin MM, Mohd-Azmi ML. Bala JA, et al. Among authors: mohamed rb. Infect Genet Evol. 2020 Jan;77:104076. doi: 10.1016/j.meegid.2019.104076. Epub 2019 Oct 31. Infect Genet Evol. 2020. PMID: 31678648
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