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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1968 1
1969 1
1970 1
1976 4
1977 2
1978 5
1979 4
1980 2
1981 3
1982 7
1983 8
1984 3
1985 1
1986 2
1987 7
1988 5
1989 5
1990 12
1991 7
1992 16
1993 9
1994 8
1995 9
1996 17
1997 24
1998 26
1999 25
2000 36
2001 31
2002 37
2003 35
2004 49
2005 41
2006 54
2007 74
2008 62
2009 55
2010 74
2011 68
2012 77
2013 76
2014 76
2015 86
2016 86
2017 109
2018 130
2019 117
2020 118
2021 135
2022 134
2023 156
2024 56

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1,912 results

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Quoted phrase not found in phrase index: "Cataract 18"
Page 1
Carotenoids in human nutrition and health.
Eggersdorfer M, Wyss A. Eggersdorfer M, et al. Arch Biochem Biophys. 2018 Aug 15;652:18-26. doi: 10.1016/j.abb.2018.06.001. Epub 2018 Jun 6. Arch Biochem Biophys. 2018. PMID: 29885291 Review.
The benefit of lutein in reducing progression of age-related macular eye disease and cataracts is strengthening; an intake recommendation would help to generate awareness in the general population to have an adequate intake of lutein rich foods. ...
The benefit of lutein in reducing progression of age-related macular eye disease and cataracts is strengthening; an intake recommenda …
The Complications of Myopia: A Review and Meta-Analysis.
Haarman AEG, Enthoven CA, Tideman JWL, Tedja MS, Verhoeven VJM, Klaver CCW. Haarman AEG, et al. Invest Ophthalmol Vis Sci. 2020 Apr 9;61(4):49. doi: 10.1167/iovs.61.4.49. Invest Ophthalmol Vis Sci. 2020. PMID: 32347918 Free PMC article.
PURPOSE: To determine the risk between degree of myopia and myopic macular degeneration (MMD), retinal detachment (RD), cataract, open angle glaucoma (OAG), and blindness. METHODS: A systematic review and meta-analyses of studies published before June 2019 on myopia compli …
PURPOSE: To determine the risk between degree of myopia and myopic macular degeneration (MMD), retinal detachment (RD), cataract, ope …
Cataract surgery is not associated with post-operative binocular vision anomalies in age-related cataract patients.
Tan QQ, Lewis JS, Lan CJ, Liao X, Tang XL, Wang J, Aljohani S, Scheiman MM. Tan QQ, et al. Ophthalmic Physiol Opt. 2022 Sep;42(5):998-1008. doi: 10.1111/opo.13012. Epub 2022 Jun 12. Ophthalmic Physiol Opt. 2022. PMID: 35690924 Free PMC article.
PURPOSE: To compare the binocular vision status of patients pre- and post-cataract surgery, and to investigate the risk factors for patients who develop binocular vision anomalies post-surgery. ...CONCLUSIONS: Binocular vision anomalies, especially convergence insufficienc …
PURPOSE: To compare the binocular vision status of patients pre- and post-cataract surgery, and to investigate the risk factors for p …
DeepLensNet: Deep Learning Automated Diagnosis and Quantitative Classification of Cataract Type and Severity.
Keenan TDL, Chen Q, Agrón E, Tham YC, Goh JHL, Lei X, Ng YP, Liu Y, Xu X, Cheng CY, Bikbov MM, Jonas JB, Bhandari S, Broadhead GK, Colyer MH, Corsini J, Cousineau-Krieger C, Gensheimer W, Grasic D, Lamba T, Magone MT, Maiberger M, Oshinsky A, Purt B, Shin SY, Thavikulwat AT, Lu Z, Chew EY; AREDS Deep Learning Research Group. Keenan TDL, et al. Ophthalmology. 2022 May;129(5):571-584. doi: 10.1016/j.ophtha.2021.12.017. Epub 2022 Jan 3. Ophthalmology. 2022. PMID: 34990643 Free PMC article.
PARTICIPANTS: A total of 18 999 photographs (6333 triplets) from longitudinal follow-up of 1137 eyes (576 AREDS participants). ...For PSC, mean MSE was 171.9 (SD, 38.9), compared with 176.8 (SD, 98.0; P = 0.67) for the ophthalmologists and 398.2 (SD, 645.4; P = 0.18 …
PARTICIPANTS: A total of 18 999 photographs (6333 triplets) from longitudinal follow-up of 1137 eyes (576 AREDS participants). ...For …
Congenital cataracts-facial dysmorphism-neuropathy.
Kalaydjieva L. Kalaydjieva L. Orphanet J Rare Dis. 2006 Aug 29;1:32. doi: 10.1186/1750-1172-1-32. Orphanet J Rare Dis. 2006. PMID: 16939648 Free PMC article. Review.
Congenital Cataracts Facial Dysmorphism Neuropathy (CCFDN) syndrome is a complex developmental disorder of autosomal recessive inheritance. ...Families benefit from genetic counselling and predictive testing. Management includes surgical treatment of the cataracts, …
Congenital Cataracts Facial Dysmorphism Neuropathy (CCFDN) syndrome is a complex developmental disorder of autosomal recessive inheri …
Astigmatism evaluation prior to cataract surgery.
Gupta PC, Caty JT. Gupta PC, et al. Curr Opin Ophthalmol. 2018 Jan;29(1):9-13. doi: 10.1097/ICU.0000000000000446. Curr Opin Ophthalmol. 2018. PMID: 29084004 Review.
PURPOSE OF REVIEW: To evaluate and summarize literature from the past 18 months reporting advancements and issues in astigmatism assessment prior to cataract surgery. ...
PURPOSE OF REVIEW: To evaluate and summarize literature from the past 18 months reporting advancements and issues in astigmatism asse …
Vici syndrome: a review.
Byrne S, Dionisi-Vici C, Smith L, Gautel M, Jungbluth H. Byrne S, et al. Orphanet J Rare Dis. 2016 Feb 29;11:21. doi: 10.1186/s13023-016-0399-x. Orphanet J Rare Dis. 2016. PMID: 26927810 Free PMC article. Review.
Vici syndrome [OMIM242840] is a severe, recessively inherited congenital disorder characterized by the principal features of callosal agenesis, cataracts, oculocutaneous hypopigmentation, cardiomyopathy, and a combined immunodeficiency. ...
Vici syndrome [OMIM242840] is a severe, recessively inherited congenital disorder characterized by the principal features of callosal agenes …
An Evaluation of the IOLMaster 700.
Bullimore MA, Slade S, Yoo P, Otani T. Bullimore MA, et al. Eye Contact Lens. 2019 Mar;45(2):117-123. doi: 10.1097/ICL.0000000000000552. Eye Contact Lens. 2019. PMID: 30325761
METHODS: In a clinical practice, complete measurements were taken on one eye of 100 subjects: 51 with cataracts and 49 with clear lenses. Three sets of measurements were taken by 3 operators with three different IOLMaster 700 units, and one operator took 3 measurements wit …
METHODS: In a clinical practice, complete measurements were taken on one eye of 100 subjects: 51 with cataracts and 49 with clear len …
Clinical, biochemical and molecular analysis in a cohort of individuals with gyrate atrophy.
Palmer E, Stepien KM, Campbell C, Barton S, Iosifidis C, Ghosh A, Broomfield A, Woodall A, Wilcox G, Sergouniotis PI, Black GC. Palmer E, et al. Orphanet J Rare Dis. 2023 Sep 4;18(1):265. doi: 10.1186/s13023-023-02840-0. Orphanet J Rare Dis. 2023. PMID: 37667371 Free PMC article.
The median age at diagnosis was 8 years (range 10 months - 33 years) and all cases had hyperornithinaemia (median: 800 micromoles/L; range: 458-1244 micromoles/L). Common features at presentation included high myopia (10/18) and nyctalopia (5/18). Ophthalmic finding …
The median age at diagnosis was 8 years (range 10 months - 33 years) and all cases had hyperornithinaemia (median: 800 micromoles/L; range: …
Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders.
Maroofian R, Kaiyrzhanov R, Cali E, Zamani M, Zaki MS, Ferla M, Tortora D, Sadeghian S, Saadi SM, Abdullah U, Karimiani EG, Efthymiou S, Yeşil G, Alavi S, Al Shamsi AM, Tajsharghi H, Abdel-Hamid MS, Saadi NW, Al Mutairi F, Alabdi L, Beetz C, Ali Z, Toosi MB, Rudnik-Schöneborn S, Babaei M, Isohanni P, Muhammad J, Khan S, Al Shalan M, Hickey SE, Marom D, Elhanan E, Kurian MA, Marafi D, Saberi A, Hamid M, Spaull R, Meng L, Lalani S, Maqbool S, Rahman F, Seeger J, Palculict TB, Lau T, Murphy D, Mencacci NE, Steindl K, Begemann A, Rauch A, Akbas S, Aslanger AD, Salpietro V, Yousaf H, Ben-Shachar S, Ejeskär K, Al Aqeel AI, High FA, Armstrong-Javors AE, Zahraei SM, Seifi T, Zeighami J, Shariati G, Sedaghat A, Asl SN, Shahrooei M, Zifarelli G, Burglen L, Ravelli C, Zschocke J, Schatz UA, Ghavideldarestani M, Kamel WA, Van Esch H, Hackenberg A, Taylor JC, Al-Gazali L, Bauer P, Gleeson JJ, Alkuraya FS, Lupski JR, Galehdari H, Azizimalamiri R, Chung WK, Baig SM, Houlden H, Severino M. Maroofian R, et al. Brain. 2023 Dec 1;146(12):5031-5043. doi: 10.1093/brain/awad257. Brain. 2023. PMID: 37517035 Free PMC article.
Using exome sequencing and extensive international genetic data sharing, 39 unpublished affected individuals from 18 independent families with biallelic missense variants in MED27 have been identified (29 females, mean age at last follow-up 17 12.4 years, range 0.1-45). .. …
Using exome sequencing and extensive international genetic data sharing, 39 unpublished affected individuals from 18 independent fami …
1,912 results