Results 111 to 120 of about 25,332 (224)

R91W mutation in Rpe65 leads to milder early-onset retinal dystrophy due to the generation of low levels of 11-cis-retinal [PDF]

, 2017
RPE65 is a retinal pigment epithelial protein essential for the regeneration of 11-cis-retinal, the chromophore of cone and rod visual pigments. Mutations in RPE65 lead to a spectrum of retinal dystrophies ranging from Leber's congenital amaurosis to ...
Grimm, Christian, Oberhauser, Vitus, Remé, Charlotte E., Samardzija, Marijana, Seeliger, Mathias, Tanimoto, Naoyuki, Thiersch, Markus, von Lintig, Johannes, Wenzel, Andreas   +8 more
core  

Quinine Amaurosis [PDF]

British Journal of Ophthalmology, 1955
openaire   +2 more sources

Ocular manifestations of internal carotid artery insufficiency

Indian Journal of Ophthalmology, 1987
8 cases of internal carotid artery insufficiency were studied to find out the various ophthalmic manifestations in such cases. 50% cases had ophthalmic signs and symptoms.
Nath Rajiv, Mehra M, Nag D, Agarwal J
doaj  

Prevention of spontaneous diabetes in BB rats with FK 506 [PDF]

, 1990
A.L. Drash, Assan, Brayman, D. Mintz, I. Lieberman, Kino, Laupacis, Like, M. Nalesnik, N. Murase, S. Todo, Starzl, Stiller, Stiller, T.E. Starzl, Yale   +15 more
core   +1 more source

Molecular confirmation of the causes of inherited visual impairment in Northern Pakistan [PDF]

, 2009
Families with inherited visual impairment were identified and examined from January 2000 to December 2005 and given a clinical diagnosis. Known genes and loci were screened for mutations or linkage at Institute of Ophthalmology and Neurosciences ...
Adhi, Mehreen, Inglehearn, Chris F, Jafri, Syed Hussain, McKibbin, Martin, Rashid, Yasmin   +4 more
core   +2 more sources

Seven novel variants expand the spectrum of RPE65-related Leber congenital amaurosis in the Chinese population

Molecular Vision, 2019
Purpose: To screen RPE65 in 187 families with Leber congenital amaurosis (LCA). Methods: Sanger sequencing and/or targeted exome sequencing was employed to identify mutations in the RPE65 gene, and intrafamilial cosegregation analysis if DNA was ...
Zilin Zhong, Feng Rong, Yinghui Dai, Alakezi Yibulayin, Lin Zeng, Jian Liao, Liefeng Wang, Zhihua Huang, Zhenping Zhou, Jianjun Chen   +9 more
doaj  

Amaurosis Fugax Dolorosa: A Prodromal Syndrome in Optic Neuritis Associated With Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease. [PDF]

Neurol Neuroimmunol Neuroinflamm
Vilaseca A, Syc-Mazurek SB, Vorasoot N, Tajfirouz DA, Eggenberger E, Chodnicki KD, Pittock SJ, Chen JJ, Flanagan EP.   +8 more
europepmc   +2 more sources

Tauroursodeoxycholic acid binds to the G-protein site on light activated rhodopsin [PDF]

, 2018
Kisselev, O. G, Lobysheva, E., Marshall, G. R, Taylor, C. M   +3 more
core   +2 more sources

Rethinking the impact of amaurosis with contemporary outcomes of carotid endarterectomy among patients with transient monocular blindness. [PDF]

J Vasc Surg
Columbo JA, Martinez-Camblor P, Suckow BD, Krafcik BM, Hicks CW, Huber TS, Scali ST, Stone DH.   +7 more
europepmc   +1 more source

Intra-aortic chord and transient binocular amaurosis. [PDF]

JTCVS Tech
Cheng X, Wang Q, Li J, Song Z, Huang J.
europepmc   +1 more source