Results 141 to 150 of about 6,502 (203)

Elucidating the genetic landscape of inherited retinal disorders in India. [PDF]

Hum Genomics
Mathias GP, Raj Rajendran K, Selot R, Shetty R, Kumaramanickavel G, Ghosh A, Ghosh A.   +6 more
europepmc   +1 more source

Genetic Spectrum of Negative Electroretinograms in a Predominantly Pediatric Cohort of 177 Patients. [PDF]

Invest Ophthalmol Vis Sci
Zaslavsky K, Tumber A, Millar E, Boginskaia O, MacDonald H, Klatt R, Ali A, Heon E, Vincent A.   +8 more
europepmc   +1 more source

Long-term surgical outcome of high myopic full-thickness macular hole without retinoschisis. [PDF]

BMC Ophthalmol
Cho SD, Lee EK, Yoon CK, Park UC.
europepmc   +1 more source

A case of bilateral stellate nonhereditary idiopathic foveomacular retinoschisis with 14-month follow-up: clinical features, OCT findings and treatment outcome. [PDF]

BMC Ophthalmol
Hassanpoor N, Tahmasebi A, Aminsobhani E, Niyousha M.   +3 more
europepmc   +1 more source

Surgical Outcomes of Vitrectomy with Flower-Petal Fovea-Sparing Inverted Internal Limiting Membrane Flap Technique for Myopic Tractional Maculopathy with Retinal Detachment: A Retrospective Study. [PDF]

J Clin Med
Suh H, Park YH, Park YG.
europepmc   +1 more source

Profound Effect of Light on Cysts in X-Linked Retinoschisis. [PDF]

Invest Ophthalmol Vis Sci
Hassan S, Stanley ST, Brandauer E, Hsu Y, Rankin TJ, Laird J, Lobeck B, Thompson JM, Bengen MA, Wang K, Drack AV.   +10 more
europepmc   +1 more source

Hypotony after 25-gauge pars plana vitrectomy with suturing all sclerotomies. [PDF]

PLoS One
Takahashi S, Ueda-Consolvo T, Takata Y, Ishida M, Yanagisawa S, Hayashi A.   +5 more
europepmc   +1 more source

Idiopathic Giant Retinal Cyst: A Case Report. [PDF]

Case Rep Ophthalmol
Kacerik M, Sustykevicova Z.
europepmc   +1 more source

Amniotic membrane placement without endotamponade for optic nerve coloboma with extensive serous retinal detachment in papillorenal syndrome: A case report. [PDF]

Am J Ophthalmol Case Rep
Lucchini S, Carini E, Premi E, Ranno S, Govetto A, Radice P.   +5 more
europepmc   +1 more source

Characterisation and prevalence of inherited retinal diseases in the Finnish population reveals enrichment of population-specific phenotypes and causative variants. [PDF]

Br J Ophthalmol
Lähteenoja L, Ohtonen P, Falck A, Rahikkala EJ.   +3 more
europepmc   +1 more source