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Page 1
Vogt-Koyanagi-Harada disease.
Joye A, Suhler E. Joye A, et al. Curr Opin Ophthalmol. 2021 Nov 1;32(6):574-582. doi: 10.1097/ICU.0000000000000809. Curr Opin Ophthalmol. 2021. PMID: 34545845 Review.
PURPOSE OF REVIEW: Here, we provide an overview of Vogt-Koyanagi-Harada disease (VKH), including recent updates in our understanding of disease pathophysiology, classification and therapeutics. ...Multimodal imaging is indispensable in the initi …
PURPOSE OF REVIEW: Here, we provide an overview of Vogt-Koyanagi-Harada disease (VKH), including recent updates …
Vogt-Koyanagi-Harada disease.
O'Keefe GA, Rao NA. O'Keefe GA, et al. Surv Ophthalmol. 2017 Jan-Feb;62(1):1-25. doi: 10.1016/j.survophthal.2016.05.002. Epub 2016 May 27. Surv Ophthalmol. 2017. PMID: 27241814 Review.
Vogt-Koyanagi-Harada disease presents clinically in 4 different phases: prodromal, uveitic, convalescent, and recurrent, with extraocular manifestations including headache, meningismus, hearing loss, poliosis, and vitiligo, to varying degrees. ...Patie
Vogt-Koyanagi-Harada disease presents clinically in 4 different phases: prodromal, uveitic, convalescent, and re
Vogt-Koyanagi-Harada disease.
Burkholder BM. Burkholder BM. Curr Opin Ophthalmol. 2015 Nov;26(6):506-11. doi: 10.1097/ICU.0000000000000206. Curr Opin Ophthalmol. 2015. PMID: 26448042 Review.
PURPOSE OF REVIEW: The purpose of this article is to review the current literature on Vogt-Koyanagi-Harada (VKH) disease, including current treatment options and new research directions. RECENT FINDINGS: Recent publications on VKH disease show a …
PURPOSE OF REVIEW: The purpose of this article is to review the current literature on Vogt-Koyanagi-Harada (VKH) dis
Epidemiology of Pediatric Uveitis.
Gentile P, Ragusa E, Bolletta E, De Simone L, Gozzi F, Cappella M, Fastiggi M, De Fanti A, Cimino L. Gentile P, et al. Ocul Immunol Inflamm. 2023 Dec;31(10):2050-2059. doi: 10.1080/09273948.2023.2271988. Epub 2023 Dec 14. Ocul Immunol Inflamm. 2023. PMID: 37922466 Review.
In low- and middle-income countries, posterior uveitis and panuveitis are prevalent due to the higher rates of infectious etiologies and systemic diseases such as Behcet disease and Vogt-Koyanagi-Harada disease. In recent decades, idiopathic uve …
In low- and middle-income countries, posterior uveitis and panuveitis are prevalent due to the higher rates of infectious etiologies and sys …
Vogt-Koyanagi-Harada disease.
Cunningham ET Jr, Rathinam SR, Tugal-Tutkun I, Muccioli C, Zierhut M. Cunningham ET Jr, et al. Ocul Immunol Inflamm. 2014 Aug;22(4):249-52. doi: 10.3109/09273948.2014.939530. Ocul Immunol Inflamm. 2014. PMID: 25014114 Review. No abstract available.
[Vogt-Koyanagi-Harada disease].
Bonnet C, Daudin JB, Monnet D, Brézin A. Bonnet C, et al. J Fr Ophtalmol. 2017 Jun;40(6):512-519. doi: 10.1016/j.jfo.2017.02.006. Epub 2017 Jun 1. J Fr Ophtalmol. 2017. PMID: 28579215 Review. French.
Vogt-Koyanagi-Harada (VKH) disease is defined as a severe bilateral, chronic granulomatous panuveitis associated with serous retinal detachments, disk edema, and vitritis, with central nervous system, auditory, and integumentary manifestations. It is a
Vogt-Koyanagi-Harada (VKH) disease is defined as a severe bilateral, chronic granulomatous panuveitis associated
Vogt-Koyanagi-Harada syndrome.
Greco A, Fusconi M, Gallo A, Turchetta R, Marinelli C, Macri GF, De Virgilio A, de Vincentiis M. Greco A, et al. Autoimmun Rev. 2013 Sep;12(11):1033-8. doi: 10.1016/j.autrev.2013.01.004. Epub 2013 Apr 6. Autoimmun Rev. 2013. PMID: 23567866 Review.
OBJECTIVES: The objectives of this study are to review our current knowledge of the aetiopathogenesis of Vogt-Koyanagi-Harada syndrome, including viral infection, genetic factors and immunomediated mechanisms, and to discuss pathogenesis and its releva …
OBJECTIVES: The objectives of this study are to review our current knowledge of the aetiopathogenesis of Vogt-Koyanagi-Hara
Vogt-Koyanagi-Harada disease.
Read RW, Rao NA, Cunningham ET. Read RW, et al. Curr Opin Ophthalmol. 2000 Dec;11(6):437-42. doi: 10.1097/00055735-200012000-00009. Curr Opin Ophthalmol. 2000. PMID: 11141638 Review.
Vogt-Koyanagi-Harada (VKH) disease affects primarily persons who are Asian, Latino, Native American, or Asian Indian. Women appear to be affected more commonly than men, and VKH disease may occur at all ages, including childhood. Experimental da
Vogt-Koyanagi-Harada (VKH) disease affects primarily persons who are Asian, Latino, Native American, or Asian In
Vogt-Koyanagi-Harada disease.
Damico FM, Kiss S, Young LH. Damico FM, et al. Semin Ophthalmol. 2005 Jul-Sep;20(3):183-90. doi: 10.1080/08820530500232126. Semin Ophthalmol. 2005. PMID: 16282153 Review.
Vogt-Koyanagi-Harada disease (VKH) is a multisystem autoimmune disorder principally affecting pigmented tissues in the ocular, auditory, integumentary and central nervous systems. ...Depending on revised diagnostic criteria, the disease is class
Vogt-Koyanagi-Harada disease (VKH) is a multisystem autoimmune disorder principally affecting pigmented tissues
Uveitis genetics.
Hou S, Li N, Liao X, Kijlstra A, Yang P. Hou S, et al. Exp Eye Res. 2020 Jan;190:107853. doi: 10.1016/j.exer.2019.107853. Epub 2019 Oct 25. Exp Eye Res. 2020. PMID: 31669406 Free article. Review.
Uveitis is usually considered as a vision-threatening multiple system intraocular inflammatory disease. Among uveitis, Vogt-Koyanagi-Harada (VKH) disease and Behcet's disease (BD) are common non-infectious uveitis entities. Although the e …
Uveitis is usually considered as a vision-threatening multiple system intraocular inflammatory disease. Among uveitis, Vogt- …
155 results