In Vivo Corneal Confocal Microscopy and Histopathology of Keratitis Fugax Hereditaria From a Pathogenic Variant in NLRP3
Turunen, Joni A., Immonen, Annamari T., Järvinen, Reetta-Stiina, Kawan, Sabita, Repo, Pauliina, Korsbäck, Anna, Ala-Fossi, Olli, Jaakkola, Aino M., Majander, Anna, Vesaluoma, Minna, Kivelä, Tero T.
Published in American journal of ophthalmology (01.05.2020)
Published in American journal of ophthalmology (01.05.2020)
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TCF4 trinucleotide repeat expansion in Finnish patients with Fuchs' endothelial corneal dystrophy
Pettinen, Inka‐Tuulevi, Immonen, Annamari, Rämö, Joel, Jaakkola, Aino, Krootila, Kari, Kaukonen, Maria, Lohi, Hannes, Kivelä, Tero, Turunen, Joni
Published in Acta ophthalmologica (Oxford, England) (01.12.2022)
Published in Acta ophthalmologica (Oxford, England) (01.12.2022)
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A novel missense TGFBI variant p.(Ser591Phe) in a Finnish family with variant lattice corneal dystrophy
Jaakkola, Aino Maaria, Järventausta, Petri J, Järvinen, Reetta-Stiina, Repo, Pauliina, Kivelä, Tero T, Turunen, Joni A
Published in European journal of ophthalmology (01.07.2022)
Published in European journal of ophthalmology (01.07.2022)
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In Vivo corneal confocal microscopy study of keratoendotheliitis fugax hereditaria caused by a pathogenic variant in the NLRP3 gene
Turunen, Joni, Immonen, Annamari, Järvinen, Reetta‐Stiina, Kawan, Sabita, Repo, Pauliina, Korsbäck, Anna, Jaakkola, Aino, Majander, Anna, Vesaluoma, Minna, Kivelä, Tero
Published in Acta ophthalmologica (Oxford, England) (01.12.2019)
Published in Acta ophthalmologica (Oxford, England) (01.12.2019)
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