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1966
2025

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

Year Number of Results
1966 1
1969 1
1970 1
1975 1
1976 1
1978 2
1982 1
1983 1
1985 1
1986 1
1988 2
1989 2
1990 3
1991 5
1992 3
1993 5
1994 6
1995 4
1996 1
1997 3
1998 7
1999 3
2000 2
2001 9
2002 6
2003 5
2004 7
2005 9
2006 6
2007 4
2008 7
2009 9
2010 5
2011 9
2012 7
2013 12
2014 11
2015 10
2016 11
2017 8
2018 19
2019 5
2020 13
2021 14
2022 18
2023 23
2024 16
2025 2

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272 results

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Page 1
Ciliopathies and the Kidney: A Review.
McConnachie DJ, Stow JL, Mallett AJ. McConnachie DJ, et al. Am J Kidney Dis. 2021 Mar;77(3):410-419. doi: 10.1053/j.ajkd.2020.08.012. Epub 2020 Oct 9. Am J Kidney Dis. 2021. PMID: 33039432 Free article. Review.
Disorders of vision in multiple sclerosis.
Dhanapalaratnam R, Markoulli M, Krishnan AV. Dhanapalaratnam R, et al. Clin Exp Optom. 2022 Jan;105(1):3-12. doi: 10.1080/08164622.2021.1947745. Epub 2021 Aug 4. Clin Exp Optom. 2022. PMID: 34348598 Free article. Review.
Assessment of visual pathways is critical, considering MS can involve multiple components of the visual pathway, including optic nerves, uvea, retina and occipital cortex. Optical coherence tomography is increasingly being recognised as a highly sensitive tool in detecting …
Assessment of visual pathways is critical, considering MS can involve multiple components of the visual pathway, including optic nerv …
Mitochondrial dynamics: overview of molecular mechanisms.
Tilokani L, Nagashima S, Paupe V, Prudent J. Tilokani L, et al. Essays Biochem. 2018 Jul 20;62(3):341-360. doi: 10.1042/EBC20170104. Print 2018 Jul 20. Essays Biochem. 2018. PMID: 30030364 Free PMC article. Review.
Mitochondrial fusion is driven by a two-step process with the outer mitochondrial membrane fusion mediated by mitofusins 1 and 2 followed by inner membrane fusion, mediated by optic atrophy 1. In addition to the role of membrane lipid composition, several members of …
Mitochondrial fusion is driven by a two-step process with the outer mitochondrial membrane fusion mediated by mitofusins 1 and 2 followed by …
Retinal layer segmentation in multiple sclerosis: a systematic review and meta-analysis.
Petzold A, Balcer LJ, Calabresi PA, Costello F, Frohman TC, Frohman EM, Martinez-Lapiscina EH, Green AJ, Kardon R, Outteryck O, Paul F, Schippling S, Vermersch P, Villoslada P, Balk LJ; ERN-EYE IMSVISUAL. Petzold A, et al. Lancet Neurol. 2017 Oct;16(10):797-812. doi: 10.1016/S1474-4422(17)30278-8. Epub 2017 Sep 12. Lancet Neurol. 2017. PMID: 28920886 Free article. Review.
Data were taken from cross-sectional cohorts and from one timepoint from longitudinal studies (at least 3 months after onset in studies of optic neuritis). We classified data on eyes into healthy controls, multiple-sclerosis-associated optic neuritis (MSON), …
Data were taken from cross-sectional cohorts and from one timepoint from longitudinal studies (at least 3 months after onset in studi …
The Phenotypic Continuum of ATP1A3-Related Disorders.
Vezyroglou A, Akilapa R, Barwick K, Koene S, Brownstein CA, Holder-Espinasse M, Fry AE, Németh AH, Tofaris GK, Hay E, Hughes I, Mansour S, Mordekar SR, Splitt M, Turnpenny PD, Demetriou D, Koopmann TT, Ruivenkamp CAL, Agrawal PB, Carr L, Clowes V, Ghali N, Holder SE, Radley J, Male A, Sisodiya SM, Kurian MA, Cross JH, Balasubramanian M. Vezyroglou A, et al. Neurology. 2022 Oct 4;99(14):e1511-e1526. doi: 10.1212/WNL.0000000000200927. Epub 2022 Jul 18. Neurology. 2022. PMID: 36192182 Free PMC article. Review.
BACKGROUND AND OBJECTIVES: ATP1A3 is associated with a broad spectrum of predominantly neurologic disorders, which continues to expand beyond the initially defined phenotypes of alternating hemiplegia of childhood, rapid-onset dystonia parkinsonism, and cerebellar ataxia, areflex …
BACKGROUND AND OBJECTIVES: ATP1A3 is associated with a broad spectrum of predominantly neurologic disorders, which continues to expand beyon …
Geographic atrophy: current and future therapeutic agents and practical considerations for retinal specialists.
Vakharia P, Eichenbaum D. Vakharia P, et al. Curr Opin Ophthalmol. 2024 May 1;35(3):165-169. doi: 10.1097/ICU.0000000000001046. Epub 2024 Feb 28. Curr Opin Ophthalmol. 2024. PMID: 38421937 Review.
PURPOSE OF REVIEW: Geographic atrophy (GA) from age-related macular degeneration (AMD) remains a leading cause of vision loss. ...Initial indications seem to be that pegcetacoplan therapy has higher risks of inflammation, vasculitis, and nonarteritic ischemic optic
PURPOSE OF REVIEW: Geographic atrophy (GA) from age-related macular degeneration (AMD) remains a leading cause of vision loss. ...Ini …
Delineating Wolfram-like syndrome: A systematic review and discussion of the WFS1-associated disease spectrum.
de Muijnck C, Brink JBT, Bergen AA, Boon CJF, van Genderen MM. de Muijnck C, et al. Surv Ophthalmol. 2023 Jul-Aug;68(4):641-654. doi: 10.1016/j.survophthal.2023.01.012. Epub 2023 Feb 9. Surv Ophthalmol. 2023. PMID: 36764396 Free article. Review.
Wolfram-like syndrome (WFLS) is a recently described autosomal dominant disorder with phenotypic similarities to autosomal recessive Wolfram syndrome (WS), including optic atrophy, hearing impairment, and diabetes mellitus. We summarize current literature, define th …
Wolfram-like syndrome (WFLS) is a recently described autosomal dominant disorder with phenotypic similarities to autosomal recessive Wolfram …
Pathologic Myopia.
Ohno-Matsui K. Ohno-Matsui K. Asia Pac J Ophthalmol (Phila). 2016 Nov/Dec;5(6):415-423. doi: 10.1097/APO.0000000000000230. Asia Pac J Ophthalmol (Phila). 2016. PMID: 27898445 Free article. Review.
On the basis of this study, PM has been defined as eyes having atrophic changes equal to or more severe than diffuse atrophy. Posterior staphyloma and eye deformity are important causes of developing vision-threatening complications. ...The mechanical load onto the importa …
On the basis of this study, PM has been defined as eyes having atrophic changes equal to or more severe than diffuse atrophy. Posteri …
Hereditary Retinal Dystrophy.
Hohman TC. Hohman TC. Handb Exp Pharmacol. 2017;242:337-367. doi: 10.1007/164_2016_91. Handb Exp Pharmacol. 2017. PMID: 28035529 Review.
These studies provided the essential proof-of-concept needed to advance monogenic gene therapies into clinic development; these therapies include treatments for: Leber's congenital amaurosis type 2, caused by mutations to RPE65, retinoid isomerohydrolase; choroideremia, caused by …
These studies provided the essential proof-of-concept needed to advance monogenic gene therapies into clinic development; these therapies in …
272 results