Results 21 to 30 of about 110,885 (306)
Polymorphisms in ARMS2/HTRA1 and complement genes and age-related macular degeneration in India: findings from the INDEYE study. [PDF]
, 2012 PURPOSE: Association between genetic variants in complement factor H (CFH), factor B (CFB), component 2 (C2), and in the ARMS2/HTRA1 region with age-related macular degeneration (AMD) comes mainly from studies of European ancestry and case-control ...
Chakravarthy, Usha +8 more
core +1 more source
Hepatology, EarlyView., 2022 A deleterious variant of FCHSD1 results in mTOR pathway overactivation and may cause porto‐sinusoidal vascular disorder (PSVD). The pedigree of the family demonstrated an autosomal dominant disease with variable expressivity. Whole‐genome sequencing and Sanger sequencing both validated the existence of the FCHSD1 variant and the heterozygosity of c ...
Jingxuan Shan +19 more
wiley +1 more source
Drugs associated with cataract formation represent an unmet need in cataract research
Frontiers in Medicine, 2022 Decreased light transmittance through the ocular lens, termed cataract, is a leading cause of low vision and blindness worldwide. Cataract causes significantly decreased quality of life, particularly in the elderly.
Jack Carlson +4 more
doaj +1 more source
Histidine nutrition and genotype affect cataract development in Atlantic salmon, Salmo salar L. [PDF]
, 2005 The aim of this study was to investigate effects of dietary levels of histidine (His) and iron (Fe) on cataract development in two strains of Atlantic salmon monitored through parr-smolt transformation.
Bjerkas, E +5 more
core +1 more source
Open Veterinary Journal, 2023 Background: Although ocular findings in diabetic patients are well described, prevalence data for those is unknown. Aim: To describe the prevalence of ocular findings and their association with glycemia in dogs with diabetes mellitus.
Francisco Cantero +3 more
doaj +1 more source
Pan African Medical Journal, 2020 Sutural cataract is uncommon crystalline opacities that affect Y-sutures of the fetal lens nucleus, which is usually congenital and hereditary with X-linked transmission. We report the clinical observation of a 26-year-old patient with no significant pathological history, who consults for a decrease in bilateral progressive visual acuity.
Hassan Moutei, Meriem Abdellaoui
openaire +4 more sources
Double-pass technique and compensation-comparison method in eyes with cataract [PDF]
, 2016 PURPOSE To clinically assess the objective scatter index (OSI) obtained from double-pass images and the log(s) parameter measured with the direct compensation-comparison psychophysical technique in eyes with cataract.
Almudí Cortés, Lorena +7 more
core +2 more sources
Comparing the performance of the SF-6D and the EQ-5D in different patient groups [PDF]
, 2014 Introduction: This research aims to explore the performance of the SF-6D and the EQ-5D in patients suffering from asthma, chronic obstructive pulmonary disease, cataracts, and rheumatoid arthritis.
Ferreira, Lara N. +2 more
core +1 more source
Further genetic heterogeneity for autosomal dominant human sutural cataracts [PDF]
, 2003 A unique sutural cataract was observed in a 4-generation German family to be transmitted as an isolated autosomal, dominant trait. Since mutations in the gamma-crystallin encoding CRYG genes have previously been demonstrated to be the most frequent ...
Billingsley, G. +6 more
core +1 more source
Pesquisa Veterinária Brasileira, 2010 Com o aumento do número de intervenções cirúrgicas para a remoção da catarata em cães, observa-se a necessidade de exames específicos que devem ser realizados antes da indicação cirúrgica. A catarata é uma das principais causas de cegueira em cães.
Angélica M.V. Safatle +5 more
doaj +1 more source