Saihan Z - Search Results

1

Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk gene.

Tschernutter M, Jenkins SA, Waseem NH, Saihan Z, Holder GE, Bird AC, Bhattacharya SS, Ali RR, Webster AR. Tschernutter M, et al. Among authors: saihan z. Br J Ophthalmol. 2006 Jun;90(6):718-23. doi: 10.1136/bjo.2005.084897. Br J Ophthalmol. 2006. PMID: 16714263 Free PMC article.

2

Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.

Robson AG, Saihan Z, Jenkins SA, Fitzke FW, Bird AC, Webster AR, Holder GE. Robson AG, et al. Among authors: saihan z. Br J Ophthalmol. 2006 Apr;90(4):472-9. doi: 10.1136/bjo.2005.082487. Br J Ophthalmol. 2006. PMID: 16547330 Free PMC article.

3

Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update.

Robson AG, Michaelides M, Saihan Z, Bird AC, Webster AR, Moore AT, Fitzke FW, Holder GE. Robson AG, et al. Among authors: saihan z. Doc Ophthalmol. 2008 Mar;116(2):79-89. doi: 10.1007/s10633-007-9087-4. Epub 2007 Nov 6. Doc Ophthalmol. 2008. PMID: 17985165 Free PMC article. Review.

4

Update on Usher syndrome.

Saihan Z, Webster AR, Luxon L, Bitner-Glindzicz M. Saihan Z, et al. Curr Opin Neurol. 2009 Feb;22(1):19-27. doi: 10.1097/wco.0b013e3283218807. Curr Opin Neurol. 2009. PMID: 19165952 Review.

5

Clinical and biochemical effects of the E139K missense mutation in the TIMP3 gene, associated with Sorsby fundus dystrophy.

Saihan Z, Li Z, Rice J, Rana NA, Ramsden S, Schlottmann PG, Jenkins SA, Blyth C, Black GC, McKie N, Webster AR. Saihan Z, et al. Mol Vis. 2009 Jun 15;15:1218-30. Mol Vis. 2009. PMID: 19536307 Free PMC article.

6

Mutations in the USH1C gene associated with sector retinitis pigmentosa and hearing loss.

Saihan Z, Stabej Ple Q, Robson AG, Rangesh N, Holder GE, Moore AT, Steel KP, Luxon LM, Bitner-Glindzicz M, Webster AR. Saihan Z, et al. Retina. 2011 Sep;31(8):1708-16. doi: 10.1097/IAE.0b013e31820d3fd1. Retina. 2011. PMID: 21487335

7

Comprehensive sequence analysis of nine Usher syndrome genes in the UK National Collaborative Usher Study.

Le Quesne Stabej P, Saihan Z, Rangesh N, Steele-Stallard HB, Ambrose J, Coffey A, Emmerson J, Haralambous E, Hughes Y, Steel KP, Luxon LM, Webster AR, Bitner-Glindzicz M. Le Quesne Stabej P, et al. Among authors: saihan z. J Med Genet. 2012 Jan;49(1):27-36. doi: 10.1136/jmedgenet-2011-100468. Epub 2011 Dec 1. J Med Genet. 2012. PMID: 22135276 Free PMC article.

8

Comparison of fundus autofluorescence with photopic and scotopic fine matrix mapping in patients with retinitis pigmentosa: 4- to 8-year follow-up.

Robson AG, Lenassi E, Saihan Z, Luong VA, Fitzke FW, Holder GE, Webster AR. Robson AG, et al. Among authors: saihan z. Invest Ophthalmol Vis Sci. 2012 Sep 14;53(10):6187-95. doi: 10.1167/iovs.12-10195. Invest Ophthalmol Vis Sci. 2012. PMID: 22899761

9

Natural history and retinal structure in patients with Usher syndrome type 1 owing to MYO7A mutation.

Lenassi E, Saihan Z, Cipriani V, Le Quesne Stabej P, Moore AT, Luxon LM, Bitner-Glindzicz M, Webster AR. Lenassi E, et al. Among authors: saihan z. Ophthalmology. 2014 Feb;121(2):580-7. doi: 10.1016/j.ophtha.2013.09.017. Epub 2013 Nov 5. Ophthalmology. 2014. PMID: 24199935

10

The effect of the common c.2299delG mutation in USH2A on RNA splicing.

Lenassi E, Saihan Z, Bitner-Glindzicz M, Webster AR. Lenassi E, et al. Among authors: saihan z. Exp Eye Res. 2014 May;122:9-12. doi: 10.1016/j.exer.2014.02.018. Epub 2014 Mar 4. Exp Eye Res. 2014. PMID: 24607488

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