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Eye (London, England)|February 26, 2024
A comparison of keratoconus progression following collagen cross-linkage using standard or personalised keratometry thresholdsJi-Peng Olivia Li, Howard P Maile, Catey Bunce, et al.Eye (London, England)|February 19, 2026
Influence of inflammatory and metabolic factors on keratoconus risk: a causal inference analysisPirro G Hysi, Alison J Hardcastle, Alice E Davidson, et al.Investigative Ophthalmology & Visual Science|January 8, 2015
Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconusAlice E Davidson, Edmondo Borasio, Petra Liskova, et al.Molecular Vision|October 26, 2007
Molecular analysis of the VSX1 gene in familial keratoconusPetra Liskova, Neil D Ebenezer, Pirro G Hysi, et al.Journal of the American Podiatric Medical Association|April 10, 2019
Does Immobilization Affect Braking Time?Faith A Schick, Homyar Karanjia, Nicholas Taweel, et al.Connecticut Medicine|August 24, 2005
The demographics, histopathology and patterns of treatment of anal cancer in Connecticut: 1980-2000Ioannis Hatzaras, Farshad Abir, Robert Kozol, et al.Eye (London, England)|May 13, 2024
Factors affecting anatomical and visual outcomes in Terson syndrome managed by surgery or observationBeatrice Gallo, Ramy Khader, Julia Fajardo-Sanchez, et al.American Journal of Ophthalmology|January 18, 2005
Novel CHST6 nonsense and missense mutations responsible for macular corneal dystrophyMohamed F El-Ashry, Mai M Abd El-Aziz, Osama Shalaby, et al.Human Mutation|February 14, 2015
Mutations in collagen, type XVII, alpha 1 (COL17A1) cause epithelial recurrent erosion dystrophy (ERED)Frida Jonsson, Berit Byström, Alice E Davidson, et al.European Journal of Human Genetics : EJHG|October 29, 2015
Heterozygous deletions at the ZEB1 locus verify haploinsufficiency as the mechanism of disease for posterior polymorphous corneal dystrophy type 3Petra Liskova, Cerys J Evans, Alice E Davidson, et al.Pageof 17