Results 31 to 40 of about 56,893 (104)
Kerala Journal of OphthalmologyPurpose: This study aims to evaluate the central corneal thickness (CCT), intraocular pressure (IOP), and glycemic status in uncontrolled diabetic patients at baseline, 1 week, and 12 weeks, and to examine the relationship between changes in CCT and IOP ...
Vaisna Gopi +2 more
doaj +1 more source
Kerala Journal of OphthalmologyType 1 neurofibromatosis (NF1) is an autosomal dominant multisystem disease caused by a mutation in the neurofibromin 1 gene, which affects tissues derived from the neural crest.
Sujit Das
doaj +1 more source
Kerala Journal of OphthalmologyTo report a rare case of extrusion of Aurolab aqueous drainage implant (AADI). A 65-year-old male presented with a history of blunt trauma, loss of vision, and irritation in his left eye (oculus sinister [OS]) for 1 year.
Devendra Maheshwari +4 more
doaj +1 more source
Congenital stationary night blindness linked to a CACNA1F gene mutation [PDF]
Revista Brasileira de OftalmologiaCongenital stationary night blindness encompasses a heterogeneous group of inherited retinal dystrophies characterized by impaired scotopic vision from birth.
Flávio Mac Cord Medina +4 more
doaj +1 more source
UEG Week 2019 Poster Presentations
, 2019 United European Gastroenterology Journal, Volume 7, Issue S8, Page 189-1030, October 2019.
wiley +1 more source
ОфтальмохирургияPurpose. To present the development stages and results of 18 years of experience in laser technologies application for the treatment of premature infants with active ROP in the Kaluga branch of S.
A.V. Tereshchenko +4 more
doaj +1 more source
UEG Week 2018 Poster Presentations
, 2018 United European Gastroenterology Journal, Volume 6, Issue S8, Page A135-A747, October 2018.
wiley +1 more source