Abd El-Aziz MM - Search Results

1

A clinical and molecular genetic study of autosomal-dominant stromal corneal dystrophy in British population.

El-Ashry MF, Abd El-Aziz MM, Hardcastle AJ, Bhattacharya SS, Ebenezer ND. El-Ashry MF, et al. Ophthalmic Res. 2005 Nov-Dec;37(6):310-7. doi: 10.1159/000087791. Epub 2005 Aug 23. Ophthalmic Res. 2005. PMID: 16118514

2

A clinical, histopathological, and genetic study of Avellino corneal dystrophy in British families.

El-Ashry MF, Abd El-Aziz MM, Larkin DF, Clarke B, Cree IA, Hardcastle AJ, Bhattacharya SS, Ebenezer ND. El-Ashry MF, et al. Br J Ophthalmol. 2003 Jul;87(7):839-42. doi: 10.1136/bjo.87.7.839. Br J Ophthalmol. 2003. PMID: 12812879 Free PMC article.

3

BIGH3 mutation in a Bangladeshi family with a variable phenotype of LCDI.

El-Ashry MF, Abd El-Aziz MM, Ficker LA, Hardcastle AJ, Bhattacharya SS, Ebenezer ND. El-Ashry MF, et al. Eye (Lond). 2004 Jul;18(7):723-8. doi: 10.1038/sj.eye.6701313. Eye (Lond). 2004. PMID: 15017378 Free article.

4

Identification of novel mutations in the carbohydrate sulfotransferase gene (CHST6) causing macular corneal dystrophy.

El-Ashry MF, Abd El-Aziz MM, Wilkins S, Cheetham ME, Wilkie SE, Hardcastle AJ, Halford S, Bayoumi AY, Ficker LA, Tuft S, Bhattacharya SS, Ebenezer ND. El-Ashry MF, et al. Invest Ophthalmol Vis Sci. 2002 Feb;43(2):377-82. Invest Ophthalmol Vis Sci. 2002. PMID: 11818380

5

Novel CHST6 nonsense and missense mutations responsible for macular corneal dystrophy.

El-Ashry MF, Abd El-Aziz MM, Shalaby O, Wilkins S, Poopalasundaram S, Cheetham M, Tuft SJ, Hardcastle AJ, Bhattacharya SS, Ebenezer ND. El-Ashry MF, et al. Am J Ophthalmol. 2005 Jan;139(1):192-3. doi: 10.1016/j.ajo.2004.07.001. Am J Ophthalmol. 2005. PMID: 15652851

6

Exclusion of four candidate genes, KHDRBS2, PTP4A1, KIAA1411 and OGFRL1, as causative of autosomal recessive retinitis pigmentosa.

Abd El-Aziz MM, Patel RJ, El-Ashry MF, Barragan I, Marcos I, Borrego S, Antiñolo G, Bhattacharya SS. Abd El-Aziz MM, et al. Ophthalmic Res. 2006;38(1):19-23. doi: 10.1159/000088493. Epub 2005 Sep 23. Ophthalmic Res. 2006. PMID: 16192744

7

Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus.

Abd El-Aziz MM, El-Ashry MF, Barragan I, Marcos I, Borrego S, Antiñolo G, Bhattacharya SS. Abd El-Aziz MM, et al. Curr Eye Res. 2005 Dec;30(12):1081-7. doi: 10.1080/02713680500351039. Curr Eye Res. 2005. PMID: 16354621

8

A clinical and molecular genetic study of Egyptian and Saudi Arabian patients with primary congenital glaucoma (PCG).

El-Ashry MF, Abd El-Aziz MM, Bhattacharya SS. El-Ashry MF, et al. J Glaucoma. 2007 Jan;16(1):104-11. doi: 10.1097/01.ijg.0000212288.00917.e1. J Glaucoma. 2007. PMID: 17224759

9

Molecular genetic study of Egyptian patients with macular corneal dystrophy.

El-Ashry MF, Abd El-Aziz MM, Shalaby O, Bhattacharya SS. El-Ashry MF, et al. Br J Ophthalmol. 2010 Feb;94(2):250-5. doi: 10.1136/bjo.2009.161810. Epub 2009 Sep 3. Br J Ophthalmol. 2010. PMID: 19734134

10

A novel genetic study of Chinese families with autosomal recessive retinitis pigmentosa.

Abd El-Aziz MM, El-Ashry MF, Chan WM, Chong KL, Barragan I, Antiñolo G, Pang CP, Bhattacharya SS. Abd El-Aziz MM, et al. Ann Hum Genet. 2007 May;71(Pt 3):281-94. doi: 10.1111/j.1469-1809.2006.00333.x. Epub 2006 Nov 29. Ann Hum Genet. 2007. PMID: 17156103

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