Tuft SJ - Search Results

1

Tuft SJ, Hassan H, George S, Frazer DG, Willoughby CE, Liskova P. Tuft SJ, et al. Acta Ophthalmol. 2012 Sep;90(6):e482-6. doi: 10.1111/j.1755-3768.2012.02448.x. Epub 2012 Jun 8. Acta Ophthalmol. 2012. PMID: 22682160 Free article.

2

Acute corneal hydrops in keratoconus.

Tuft SJ, Gregory WM, Buckley RJ. Tuft SJ, et al. Ophthalmology. 1994 Oct;101(10):1738-44. doi: 10.1016/s0161-6420(94)31110-9. Ophthalmology. 1994. PMID: 7936572

3

Prognostic factors for the progression of keratoconus.

Tuft SJ, Moodaley LC, Gregory WM, Davison CR, Buckley RJ. Tuft SJ, et al. Ophthalmology. 1994 Mar;101(3):439-47. doi: 10.1016/s0161-6420(94)31313-3. Ophthalmology. 1994. PMID: 8127564

4

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. Ramprasad VL, et al. Among authors: tuft sj. Hum Mutat. 2007 May;28(5):522-3. doi: 10.1002/humu.9487. Hum Mutat. 2007. PMID: 17397048

5

Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy.

Liskova P, Tuft SJ, Gwilliam R, Ebenezer ND, Jirsova K, Prescott Q, Martincova R, Pretorius M, Sinclair N, Boase DL, Jeffrey MJ, Deloukas P, Hardcastle AJ, Filipec M, Bhattacharya SS. Liskova P, et al. Among authors: tuft sj. Hum Mutat. 2007 Jun;28(6):638. doi: 10.1002/humu.9495. Hum Mutat. 2007. PMID: 17437275 Free PMC article.

6

Study of p.N247S KERA mutation in a British family with cornea plana.

Liskova P, Hysi PG, Williams D, Ainsworth JR, Shah S, de la Chapelle A, Tuft SJ, Bhattacharya SS. Liskova P, et al. Among authors: tuft sj. Mol Vis. 2007 Jul 27;13:1339-47. Mol Vis. 2007. PMID: 17679937

7

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. Liskova P, et al. Among authors: tuft sj. Mol Vis. 2007 Oct 4;13:1887-91. Mol Vis. 2007. PMID: 17960127 Free PMC article.

8

Sequencing of the CHST6 gene in Czech macular corneal dystrophy patients supports the evidence of a founder mutation.

Liskova P, Veraitch B, Jirsova K, Filipec M, Neuwirth A, Ebenezer ND, Hysi PG, Hardcastle AJ, Tuft SJ, Bhattacharya SS. Liskova P, et al. Among authors: tuft sj. Br J Ophthalmol. 2008 Feb;92(2):265-7. doi: 10.1136/bjo.2007.125252. Epub 2007 Oct 25. Br J Ophthalmol. 2008. PMID: 17962390

9

British family with early-onset Fuchs' endothelial corneal dystrophy associated with p.L450W mutation in the COL8A2 gene.

Liskova P, Prescott Q, Bhattacharya SS, Tuft SJ. Liskova P, et al. Among authors: tuft sj. Br J Ophthalmol. 2007 Dec;91(12):1717-8. doi: 10.1136/bjo.2007.115154. Br J Ophthalmol. 2007. PMID: 18024822 Free PMC article. No abstract available.

10

Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech families.

Liskova P, Klintworth GK, Bowling BL, Filipec M, Jirsova K, Tuft SJ, Bhattacharya SS, Hardcastle AJ, Ebenezer ND. Liskova P, et al. Among authors: tuft sj. Ophthalmic Res. 2008;40(2):105-8. doi: 10.1159/000115325. Epub 2008 Feb 6. Ophthalmic Res. 2008. PMID: 18259096

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