Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Finny T. John"'
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 27, Iss , Pp 101610- (2022)
Purpose: To report treatment of uncontrolled intraocular pressure in a patient with uveal melanoma status post plaque radiotherapy with ab interno XEN gel stent implantation. Observations: A 21-year-old female with a history of iris and ciliary body
Externí odkaz:
https://doaj.org/article/741d17c7909749349833cea3cabef640
Publikováno v:
International Ophthalmology. 41:915-922
To describe the presentation, features, and outcomes of patients with Vogt-Koyanagi-Harada disease (VKH) seen by uveitis specialists in Oklahoma. Clinical data were collected for 26 patients (52 eyes) diagnosed with VKH and seen between 1992 and 2018
Publikováno v:
Journal of Cataract and Refractive Surgery Online Case Reports. 10:e00077
Publikováno v:
International ophthalmology. 41(3)
To describe the presentation, features, and outcomes of patients with Vogt-Koyanagi-Harada disease (VKH) seen by uveitis specialists in Oklahoma.Clinical data were collected for 26 patients (52 eyes) diagnosed with VKH and seen between 1992 and 2018.
Autor:
Finny T. John, Jean R. Hausheer
Publikováno v:
Cannabis in Medicine ISBN: 9783030459673
The endocannabinoid system strongly influences a wide variety of physiologic processes within the human body by targeting specific receptors in most organ systems, including the ocular system. Glaucoma is an optic neuropathy that has a wide variety o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5d1ef947824cd0d1b8ed4b566bb4850
https://doi.org/10.1007/978-3-030-45968-0_11
https://doi.org/10.1007/978-3-030-45968-0_11
Autor:
Lea D Bennett, Kaylie D. Jones, Martin Klein, Finny T. John, David G. Birch, Bojana Radojevic
Publikováno v:
Translational Vision Science & Technology
Purpose Mutations in the inosine monophosphate dehydrogenase 1 (IMPDH1) gene are a common cause of inherited retinal degeneration (IRD). Due to species- and tissue-dependent expression of IMPDH1, there are no appropriate models of human IMPDH1 diseas