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Mutations in FYCO1 identified in families with congenital cataracts.
Iqbal H, Khan SY, Zhou L, Irum B, Ali M, Ahmed MR, Shahzad M, Ali MH, Naeem MA, Riazuddin S, Hejtmancik JF, Riazuddin SA. Iqbal H, et al. Among authors: ali m, ali mh. Mol Vis. 2020 Apr 28;26:334-344. eCollection 2020. Mol Vis. 2020. PMID: 32355443 Free PMC article.
Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening.
Chen J, Wang Q, Cabrera PE, Zhong Z, Sun W, Jiao X, Chen Y, Govindarajan G, Naeem MA, Khan SN, Ali MH, Assir MZ, Rahman FU, Qazi ZA, Riazuddin S, Akram J, Riazuddin SA, Hejtmancik JF. Chen J, et al. Among authors: ali mh. Invest Ophthalmol Vis Sci. 2017 Apr 1;58(4):2207-2217. doi: 10.1167/iovs.17-21469. Invest Ophthalmol Vis Sci. 2017. PMID: 28418495 Free PMC article.
A missense allele of PEX5 is responsible for the defective import of PTS2 cargo proteins into peroxisomes.
Ali M, Khan SY, Rodrigues TA, Francisco T, Jiao X, Qi H, Kabir F, Irum B, Rauf B, Khan AA, Mehmood A, Naeem MA, Assir MZ, Ali MH, Shahzad M, Abu-Amero KK, Akram SJ, Akram J, Riazuddin S, Riazuddin S, Robinson ML, Baes M, Azevedo JE, Hejtmancik JF, Riazuddin SA. Ali M, et al. Among authors: ali mh. Hum Genet. 2021 Apr;140(4):649-666. doi: 10.1007/s00439-020-02238-z. Epub 2021 Jan 2. Hum Genet. 2021. PMID: 33389129
Challenges in the management of glaucoma in developing countries.
Butt NH, Ayub MH, Ali MH. Butt NH, et al. Among authors: ali mh. Taiwan J Ophthalmol. 2016 Jul-Sep;6(3):119-122. doi: 10.1016/j.tjo.2016.01.004. Epub 2016 Apr 20. Taiwan J Ophthalmol. 2016. PMID: 29018725 Free PMC article. Review.
Ophthalmic Manifestations of Acute Leukemia.
Hafeez MU, Ali MH, Najib N, Ayub MH, Shafi K, Munir M, Butt NH. Hafeez MU, et al. Among authors: ali mh. Cureus. 2019 Jan 7;11(1):e3837. doi: 10.7759/cureus.3837. Cureus. 2019. PMID: 30891378 Free PMC article.
407 results