Results 111 to 120 of about 7,016 (169)

Brain derived neurotrophic factor keeps pattern electroretinogram from dropping after superior colliculus lesion in mice.

Int J Ophthalmol, 2016
Yang BB, Yang X, Ding HY.
europepmc   +1 more source

Genotype-phenotype correlations in Chinese patients with congenital stationary night blindness and early-onset high myopia: evidence from electrophysiology and whole-exome sequencing. [PDF]

Int J Ophthalmol
Qi R, Zhou Q, Ma MJ, Lian YY, Rong WN, Sheng XL.   +5 more
europepmc   +1 more source

Expanding the Genotypic Landscape of Congenital Stationary Night Blindness in an Ethnically Diverse Canadian Population. [PDF]

Hum Mutat
Ling J, Pindwarawala M, Gregory-Evans CY, Kirby M, Gregory-Evans K.   +4 more
europepmc   +1 more source

Unilateral Retinitis Pigmentosa, Glial Tissue Abnormality, and Microphthalmia in a Young Female Patient: A Case Report. [PDF]

Cureus
Bivona L, Rama T, Wolfe GJ, Maris PJ, Lopez R.   +4 more
europepmc   +1 more source

Effects of nicotinamide supplementation in normal-tension glaucoma: a crossover placebo-controlled randomised clinical trial. [PDF]

Br J Ophthalmol
Ha A, Kim YK, Lee CK, Williams PA, Morgan JE, Shin YI, Kim E, Kim M, Rho S.   +8 more
europepmc   +1 more source

Multimodal imaging of stellate nonhereditary idiopathic foveomacular retinoschisis with midperipheral retinoschisis and microvasculopathy. [PDF]

Am J Ophthalmol Case Rep
Bourdin A, Audo I, Benadji A, Fajnkuchen F, Paques M, Mrejen S.   +5 more
europepmc   +1 more source

Short-Term Effects of Low-Level Red-Light Therapy on Central Retinal Function: A Combined Pattern ERG and Photopic ERG Study. [PDF]

Vision (Basel)
Qasim M, Fernandes P, Jorge J.
europepmc   +1 more source

Identification of novel mutations in the <i>GRK1</i> gene in an Algerian family with Oguchi disease. [PDF]

Int J Ophthalmol
Molina Martín JC, García GPG, Campos Mollo E, García Navarro MM, Molina Martín LA, Desco Esteban C, Piñero DP.   +6 more
europepmc   +1 more source