Corneal endothelial assessment in xeroderma pigmentosum: a case–control study
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
https://link.springer.com/content/pdf/10.1007/s10792-020-01398-1.pdf
Reference21 articles.
1. Kraemer KH, Patronas NJ, Schiffmann R et al (2007) Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype–phenotype relationship. Neuroscience 145:1388–1396
2. Kraemer KH, Lee MM, Scotto J (1987) Xeroderma pigmentosum. Cutaneous, ocular, and neurologic abnormalities in 830 published cases. Arch Dermatol 123:241–250
3. Brooks BP, Thompson AH, Bishop RJ et al (2013) Ocular manifestations of xeroderma pigmentosum: long-term follow-up highlights the role of DNA repair in protection from sun damage. Ophthalmology 120(7):1324–1336
4. Chaurasia S, Mulay K, Ramappa M, Sangwan V, Murthy S, Nair R, Vemuganti G (2014) Corneal changes in xeroderma pigmentosum: a clinicopathologic report. Am J Ophthalmol 157(2):495–500
5. Vira D, Fernandes M, Mittal R (2016) Descemet stripping automated endothelial keratoplasty for endothelial dysfunction in xeroderma pigmentosum: a clinicopathological correlation and review of literature. Eye Contact Lens 42(4):e17–e19
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