PubMed

Molecular Genetic Study of Egyptian Patients with Macular Corneal Dystrophy.

El-Ashry MF, Abd El-Aziz MM, Shalaby O, Bhattacharya S.

Br J Ophthalmol. 2009 Sep 3. [Epub ahead of print]PMID: 19734134 [PubMed - as supplied by publisher]Related articles

The article by Fintak et al on the incidence of endophthalmitis related to intravitreal injection of bevacizumab and ranibizumab.

El-Ashry MF, Dhillon B.

Retina. 2009 May;29(5):720-1; author reply 721-2. No abstract available. PMID: 19430287 [PubMed - indexed for MEDLINE]Related articles

EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa.

Abd El-Aziz MM, Barragan I, O'Driscoll CA, Goodstadt L, Prigmore E, Borrego S, Mena M, Pieras JI, El-Ashry MF, Safieh LA, Shah A, Cheetham ME, Carter NP, Chakarova C, Ponting CP, Bhattacharya SS, Antinolo G.

Nat Genet. 2008 Nov;40(11):1285-7. Epub 2008 Oct 5.PMID: 18836446 [PubMed - indexed for MEDLINE]Related articlesFree article

Linkage validation of RP25 Using the 10K genechip array and further refinement of the locus by new linked families.

Barragán I, Abd El-Aziz MM, Borrego S, El-Ashry MF, O'Driscoll C, Bhattacharya SS, Antiñolo G.

Ann Hum Genet. 2008 Jul;72(Pt 4):454-62. Epub 2007 May 29.PMID: 18510647 [PubMed - indexed for MEDLINE]Related articles

Large-scale molecular analysis of a 34 Mb interval on chromosome 6q: major refinement of the RP25 interval.

Abd El-Aziz MM, Barragan I, O'Driscoll C, Borrego S, Abu-Safieh L, Pieras JI, El-Ashry MF, Prigmore E, Carter N, Antinolo G, Bhattacharya SS.

Ann Hum Genet. 2008 Jul;72(Pt 4):463-77. Epub 2007 May 29.PMID: 18510646 [PubMed - indexed for MEDLINE]Related articlesFree article

Molecular analysis of the VSX1 gene in familial keratoconus.

Liskova P, Ebenezer ND, Hysi PG, Gwilliam R, El-Ashry MF, Moodaley LC, Hau S, Twa M, Tuft SJ, Bhatacharya SS.

Mol Vis. 2007 Oct 4;13:1887-91.PMID: 17960127 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRs.

Barragán I, Borrego S, Abd El-Aziz MM, El-Ashry MF, Abu-Safieh L, Bhattacharya SS, Antiñolo G.

Ann Hum Genet. 2008 Jan;72(Pt 1):26-34. Epub 2007 Sep 5.PMID: 17803723 [PubMed - indexed for MEDLINE]Related articles

Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online.

Ramprasad VL, Ebenezer ND, Aung T, Rajagopal R, Yong VH, Tuft SJ, Viswanathan D, El-Ashry MF, Liskova P, Tan DT, Bhattacharya SS, Kumaramanickavel G, Vithana EN.

Hum Mutat. 2007 May;28(5):522-3.PMID: 17397048 [PubMed - indexed for MEDLINE]Related articles

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.

J Glaucoma. 2007 Jan;16(1):104-11.PMID: 17224759 [PubMed - indexed for MEDLINE]Related articles

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.

Ann Hum Genet. 2007 May;71(Pt 3):281-94. Epub 2006 Nov 29.PMID: 17156103 [PubMed - indexed for MEDLINE]Related articles

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.

Curr Eye Res. 2005 Dec;30(12):1081-7.PMID: 16354621 [PubMed - indexed for MEDLINE]Related articles

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.

Ophthalmic Res. 2006;38(1):19-23. Epub 2005 Sep 23.PMID: 16192744 [PubMed - indexed for MEDLINE]Related articles

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.

Ophthalmic Res. 2005 Nov-Dec;37(6):310-7. Epub 2005 Aug 23.PMID: 16118514 [PubMed - indexed for MEDLINE]Related articles

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.

Am J Ophthalmol. 2005 Jan;139(1):192-3.PMID: 15652851 [PubMed - indexed for MEDLINE]Related articles

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.

Eye (Lond). 2004 Jul;18(7):723-8.PMID: 15017378 [PubMed - indexed for MEDLINE]Related articles

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.

Br J Ophthalmol. 2003 Jul;87(7):839-42.PMID: 12812879 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Invest Ophthalmol Vis Sci. 2002 Feb;43(2):377-82.PMID: 11818380 [PubMed - indexed for MEDLINE]Related articlesFree article

A novel keratocan mutation causing autosomal recessive cornea plana.

Lehmann OJ, El-ashry MF, Ebenezer ND, Ocaka L, Francis PJ, Wilkie SE, Patel RJ, Ficker L, Jordan T, Khaw PT, Bhattacharya SS.

Invest Ophthalmol Vis Sci. 2001 Dec;42(13):3118-22.PMID: 11726611 [PubMed - indexed for MEDLINE]Related articlesFree article