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137 results
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Molecular genetics of primary congenital glaucoma in Brazil.
Stoilov IR, Costa VP, Vasconcellos JP, Melo MB, Betinjane AJ, Carani JC, Oltrogge EV, Sarfarazi M. Stoilov IR, et al. Among authors: sarfarazi m. Invest Ophthalmol Vis Sci. 2002 Jun;43(6):1820-7. Invest Ophthalmol Vis Sci. 2002. PMID: 12036985
Common Molecular Challenges in Glaucoma.
Sarfarazi M. Sarfarazi M. J Ophthalmic Vis Res. 2015 Apr-Jun;10(2):95-7. doi: 10.4103/2008-322X.163767. J Ophthalmic Vis Res. 2015. PMID: 26425307 Free PMC article. No abstract available.
Genotype and phenotype correlations in congenital glaucoma.
Hollander DA, Sarfarazi M, Stoilov I, Wood IS, Fredrick DR, Alvarado JA. Hollander DA, et al. Among authors: sarfarazi m. Trans Am Ophthalmol Soc. 2006;104:183-95. Trans Am Ophthalmol Soc. 2006. PMID: 17471339 Free PMC article.
CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.
Chitsazian F, Tusi BK, Elahi E, Saroei HA, Sanati MH, Yazdani S, Pakravan M, Nilforooshan N, Eslami Y, Mehrjerdi MA, Zareei R, Jabbarvand M, Abdolahi A, Lasheyee AR, Etemadi A, Bayat B, Sadeghi M, Banoei MM, Ghafarzadeh B, Rohani MR, Rismanchian A, Thorstenson Y, Sarfarazi M. Chitsazian F, et al. Among authors: sarfarazi m. J Mol Diagn. 2007 Jul;9(3):382-93. doi: 10.2353/jmoldx.2007.060157. J Mol Diagn. 2007. PMID: 17591938 Free PMC article.
Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil.
de Melo MB, Mandal AK, Tavares IM, Ali MH, Kabra M, de Vasconcellos JP, Senthil S, Sallum JM, Kaur I, Betinjane AJ, Moura CR, Paula JS, Costa KA, Sarfarazi M, Paolera MD, Finzi S, Ferraz VE, Costa VP, Belfort R Jr, Chakrabarti S. de Melo MB, et al. Among authors: sarfarazi m. PLoS One. 2015 May 15;10(5):e0127147. doi: 10.1371/journal.pone.0127147. eCollection 2015. PLoS One. 2015. PMID: 25978063 Free PMC article.
137 results