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IC3D classification of corneal dystrophies--edition 2.
Weiss JS, Møller HU, Aldave AJ, Seitz B, Bredrup C, Kivelä T, Munier FL, Rapuano CJ, Nischal KK, Kim EK, Sutphin J, Busin M, Labbé A, Kenyon KR, Kinoshita S, Lisch W. Weiss JS, et al. Cornea. 2015 Feb;34(2):117-59. doi: 10.1097/ICO.0000000000000307. Cornea. 2015. PMID: 25564336 Free article.
BAP1 Germline Mutations in Finnish Patients with Uveal Melanoma.
Turunen JA, Markkinen S, Wilska R, Saarinen S, Raivio V, Täll M, Lehesjoki AE, Kivelä TT. Turunen JA, et al. Among authors: kivela tt. Ophthalmology. 2016 May;123(5):1112-7. doi: 10.1016/j.ophtha.2016.01.008. Epub 2016 Feb 12. Ophthalmology. 2016. PMID: 26876698
Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 (NLRP3) Gene.
Turunen JA, Wedenoja J, Repo P, Järvinen RS, Jäntti JE, Mörtenhumer S, Riikonen AS, Lehesjoki AE, Majander A, Kivelä TT. Turunen JA, et al. Among authors: kivela tt. Am J Ophthalmol. 2018 Apr;188:41-50. doi: 10.1016/j.ajo.2018.01.017. Epub 2018 Jan 31. Am J Ophthalmol. 2018. PMID: 29366613 Free article.
323 results