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Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations.
Yahia A, Hamed AAA, Mohamed IN, Elseed MA, Salih MA, El-Sadig SM, Siddig HE, Nasreldien AEM, Abdullah MA, Elzubair M, Omer FY, Bakhiet AM, Abubaker R, Abozar F, Adil R, Emad S, Musallam MA, Eltazi IZM, Omer Z, Malik H, Mohamed MOE, Elhassan AA, Mohamed EOE, Ahmed AKMA, Ahmed EAA, Eltaraifee E, Hussein BK, Abd Allah ASI, Salah L, Nimir M, Tag Elseed OM, Elhassan TEA, Elbashier A, Alfadul ESA, Fadul M, Ali KF, Taha SOMA, Bushara EE, Amin M, Koko M, Ibrahim ME, Ahmed AE, Elsayed LEO, Stevanin G. Yahia A, et al. Among authors: mohamed in. Eur J Hum Genet. 2024 Oct;32(10):1214-1226. doi: 10.1038/s41431-023-01344-6. Epub 2023 Apr 3. Eur J Hum Genet. 2024. PMID: 37012327 Free PMC article.
Sudanese female doctors in paediatrics.
Mohamed IN, Abdelraheem MB, Abdullah MA. Mohamed IN, et al. Sudan J Paediatr. 2012;12(2):36-43. Sudan J Paediatr. 2012. PMID: 27493343 Free PMC article.
Prevalence of epilepsy in 74,949 school children in Khartoum State, Sudan.
Mohamed IN, Elseed MA, Hamed AA, Abdel-Rahman ME, El-Sadig SM, Omer IM, Osman AH, Ahmed AE, Karrar ZA, Salih MA. Mohamed IN, et al. Paediatr Int Child Health. 2017 Aug;37(3):188-192. doi: 10.1080/20469047.2016.1278110. Epub 2017 Feb 6. Paediatr Int Child Health. 2017. PMID: 28162058
95 results