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Clinical heterogeneity in retinitis pigmentosa caused by variants in RP1 and RLBP1 in five extended consanguineous pedigrees.
Mol Vis. 2020 Jun 19;26:445-458. eCollection 2020.
Mol Vis. 2020.
PMID: 32587456
Free PMC article.
Novel CERKL variant in consanguineous Jordanian pedigrees with inherited retinal dystrophies.
Azab B, Barham R, Ali D, Dardas Z, Rashdan L, Bijawi M, Maswadi R, Awidi A, Jafar H, Abu-Ameerh M, Al-Bdour M, Amr S, Awidi A.
Azab B, et al. Among authors: maswadi r.
Can J Ophthalmol. 2019 Feb;54(1):51-59. doi: 10.1016/j.jcjo.2018.02.018. Epub 2018 Apr 10.
Can J Ophthalmol. 2019.
PMID: 30851774
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Unique Variant Spectrum in a Jordanian Cohort with Inherited Retinal Dystrophies.
Azab B, Dardas Z, Aburizeg D, Al-Bdour M, Abu-Ameerh M, Saleh T, Barham R, Maswadi R, Ababneh NA, Alsalem M, Zouk H, Amr S, Awidi A.
Azab B, et al. Among authors: maswadi r.
Genes (Basel). 2021 Apr 19;12(4):593. doi: 10.3390/genes12040593.
Genes (Basel). 2021.
PMID: 33921607
Free PMC article.
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Cataract Surgical Services in Palestine.
Maswadi R, Bascaran C, Clare G, Ramadan MA, Al Talbishi A, Foster A.
Maswadi R, et al.
Ophthalmic Epidemiol. 2022 Apr;29(2):223-231. doi: 10.1080/09286586.2021.1923755. Epub 2021 Jun 13.
Ophthalmic Epidemiol. 2022.
PMID: 34121602
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Effectiveness of interventions to increase uptake and completion of treatment for diabetic retinopathy in low- and middle-income countries: a rapid review protocol.
Bascaran C, Mwangi N, D'Esposito F, Cleland C, Gordon I, Ulloa JAL, Maswadi R, Mdala S, Ramke J, Evans JR, Burton M.
Bascaran C, et al. Among authors: maswadi r.
Syst Rev. 2021 Jan 14;10(1):27. doi: 10.1186/s13643-020-01562-9.
Syst Rev. 2021.
PMID: 33446272
Free PMC article.
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