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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.
Tugal-Tutkun I, Smit DP, Abu El-Asrar AM, Herbort CP Jr, Thorne JE. Tugal-Tutkun I, et al. Ocul Immunol Inflamm. 2024 May;32(4):363-366. doi: 10.1080/09273948.2024.2331401. Epub 2024 Apr 24. Ocul Immunol Inflamm. 2024. PMID: 38657222 No abstract available.
Classification Criteria for Vogt-Koyanagi-Harada Disease.
Standardization of Uveitis Nomenclature (SUN) Working Group. Standardization of Uveitis Nomenclature (SUN) Working Group. Am J Ophthalmol. 2021 Aug;228:205-211. doi: 10.1016/j.ajo.2021.03.036. Epub 2021 Apr 9. Am J Ophthalmol. 2021. PMID: 33845018 Free PMC article.
PURPOSE: To determine classification criteria for Vogt-Koyanagi-Harada (VKH) disease. DESIGN: Machine learning of cases with VKH disease and 5 other panuveitides. ...
PURPOSE: To determine classification criteria for Vogt-Koyanagi-Harada (VKH) disease. DESIGN: Machine learning o …
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.
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 …
[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 disease.
Street D, Sivaguru A, Sreekantam S, Mollan SP. Street D, et al. Pract Neurol. 2019 Aug;19(4):364-367. doi: 10.1136/practneurol-2018-002152. Epub 2019 Mar 19. Pract Neurol. 2019. PMID: 30890584
Vogt-Koyanagi-Harada disease is a rare, multisystem, autoimmune disorder with numerous clinical manifestations, mediated through a T-helper 1 response against melanocytes in the eye, inner ear, central nervous system, hair and skin. ...Following treatm …
Vogt-Koyanagi-Harada disease is a rare, multisystem, autoimmune disorder with numerous clinical manifestations, …
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 in Spain.
Arriola-Villalobos P, Moll-Udina A, Carrasco-López-Brea M, Sacristan C, Capella MJ, Peiteado D, Garrote-Llordén A, Albert Fort M, Jódar Márquez M, Jacobo Gonzalez Guijarro J, Demetrio-Pablo R, Luis Sánchez Sevilla J, Carreño E, González-López J, Miguel-Escuder L, Cuadros C, Díaz-Valle D, Adan A; Contributors: VKH Spanish Study Group; Benítez Del Castillo JM, Fonollosa A, Cordero M, Martínez Costa L, Blanco-Alonso R. Arriola-Villalobos P, et al. Eur J Ophthalmol. 2022 May;32(3):1547-1554. doi: 10.1177/11206721211033477. Epub 2021 Jul 16. Eur J Ophthalmol. 2022. PMID: 34269103
PURPOSE: To describe the clinical and epidemiological characteristics of patients with Vogt-Koyanagi-Harada (VKH) disease in Spain. METHODS: This was a retrospective multicenter analysis of data from VKH patients followed for at least 6 months. ...Ethn …
PURPOSE: To describe the clinical and epidemiological characteristics of patients with Vogt-Koyanagi-Harada (VKH) di …
2,081 results