In Vivo Corneal Confocal Microscopy and Histopathology of Keratitis Fugax Hereditaria From a Pathogenic Variant in NLRP3-Reference-Cited by-同舟云学术

In Vivo Corneal Confocal Microscopy and Histopathology of Keratitis Fugax Hereditaria From a Pathogenic Variant in NLRP3

Published:2020-05 Issue: Volume:213 Page:217-225
ISSN:0002-9394
Container-title:American Journal of Ophthalmology
language:en
Short-container-title:American Journal of Ophthalmology

Author:

Turunen Joni A.^ORCID,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.

Funder

Silmäsäätiö

Silmä- ja kudospankkisäätiö

Publisher

Elsevier BV

Subject

Ophthalmology

Reference36 articles.

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3. 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;Am J Ophthalmol,2018

4. Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome;Hoffman;Nat Genet,2001

5. Transcription profiling of NOD-like receptors in the human cornea with disease;Oh;Ocul Immunol Inflamm,2017

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1. In vivo confocal microscopy evaluation of infiltrated immune cells in corneal stroma treated with cell therapy in advanced keratoconus;Journal of Ophthalmic Inflammation and Infection;2024-01-26

2. Keratitis Fugax Hereditaria Associated With a Novel NLRP3 Mutation in a Non-Finnish Patient;Cornea;2023-10-11

3. Functional consequences of pathogenic variant c.61G>C in the inflammasome geneNLRP3underlying keratitis fugax hereditaria;British Journal of Ophthalmology;2022-11-16

4. NLRP3 inflammasome and NLRP3-related autoinflammatory diseases: From cryopyrin function to targeted therapies;Frontiers in Immunology;2022-10-06

5. Keratitis fugax hereditaria: hiding in plain sight in Sweden?;Acta Ophthalmologica;2022-08-10