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

Year Number of Results
1969 1
1971 1
1979 3
1980 1
1983 1
1986 1
1987 3
1988 2
1989 9
1990 2
1991 3
1992 8
1993 3
1994 3
1995 4
1996 4
1997 5
1998 3
1999 3
2000 5
2001 6
2002 4
2003 3
2004 2
2005 6
2006 11
2007 5
2008 4
2009 4
2010 3
2011 9
2012 9
2013 5
2014 7
2015 8
2016 5
2017 7
2018 8
2019 10
2020 8
2021 7
2022 10
2023 4
2024 2

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205 results

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Page 1
Nystagmus in childhood.
Papageorgiou E, McLean RJ, Gottlob I. Papageorgiou E, et al. Pediatr Neonatol. 2014 Oct;55(5):341-51. doi: 10.1016/j.pedneo.2014.02.007. Epub 2014 Jul 31. Pediatr Neonatol. 2014. PMID: 25086850 Free article. Review.
Nystagmus can be grouped into infantile nystagmus (IN), which usually appears in the first 3-6 months of life, and acquired nystagmus (AN), which appears later. ...It is important to differentiate between infantile and acquired nystagmus. This can be a …
Nystagmus can be grouped into infantile nystagmus (IN), which usually appears in the first 3-6 months of life, and acquired …
Congenital and infantile cataract: aetiology and management.
Chan WH, Biswas S, Ashworth JL, Lloyd IC. Chan WH, et al. Eur J Pediatr. 2012 Apr;171(4):625-30. doi: 10.1007/s00431-012-1700-1. Epub 2012 Mar 1. Eur J Pediatr. 2012. PMID: 22383071 Review.
Congenital cataract is the commonest worldwide cause of lifelong visual loss in children. ...Despite early surgery and aggressive optical rehabilitation, children may still develop deprivation amblyopia, nystagmus, strabismus, and glaucoma. The diagnosis and managem …
Congenital cataract is the commonest worldwide cause of lifelong visual loss in children. ...Despite early surgery and aggressive opt …
Oculocutaneous albinism.
Grønskov K, Ek J, Brondum-Nielsen K. Grønskov K, et al. Orphanet J Rare Dis. 2007 Nov 2;2:43. doi: 10.1186/1750-1172-2-43. Orphanet J Rare Dis. 2007. PMID: 17980020 Free PMC article. Review.
The clinical spectrum of OCA ranges, with OCA1A being the most severe type with a complete lack of melanin production throughout life, while the milder forms OCA1B, OCA2, OCA3 and OCA4 show some pigment accumulation over time. Clinical manifestations include various degrees of …
The clinical spectrum of OCA ranges, with OCA1A being the most severe type with a complete lack of melanin production throughout life, while …
Leber's Congenital Amaurosis: Current Concepts of Genotype-Phenotype Correlations.
Huang CH, Yang CM, Yang CH, Hou YC, Chen TC. Huang CH, et al. Genes (Basel). 2021 Aug 19;12(8):1261. doi: 10.3390/genes12081261. Genes (Basel). 2021. PMID: 34440435 Free PMC article. Review.
Leber's congenital amaurosis (LCA), one of the most severe inherited retinal dystrophies, is typically associated with extremely early onset of visual loss, nystagmus, and amaurotic pupils, and is responsible for 20% of childhood blindness. ...
Leber's congenital amaurosis (LCA), one of the most severe inherited retinal dystrophies, is typically associated with extremely earl …
Congenital Nystagmus and Its Congeners.
Brodsky MC. Brodsky MC. J Binocul Vis Ocul Motil. 2020 Apr-Jun;70(2):63-70. doi: 10.1080/2576117X.2020.1760072. Epub 2020 May 12. J Binocul Vis Ocul Motil. 2020. PMID: 32397854 Review.
In recent years, we have made enormous strides in elucidating the phenomenology of congenital nystagmus. The purpose of this review is to briefly summarize our current understanding of congenital nystagmus in terms of its clinical symptomatology, patho …
In recent years, we have made enormous strides in elucidating the phenomenology of congenital nystagmus. The purpose of this r …
Ciliopathy: Alström Syndrome.
Tsang SH, Aycinena ARP, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:179-180. doi: 10.1007/978-3-319-95046-4_35. Adv Exp Med Biol. 2018. PMID: 30578508 Review.
Alstrom syndrome is an autosomal recessive disease with multisystem involvement, including cone-rod dystrophy, hearing loss, type 2 diabetes, insulin resistance with hyperinsulinemia, dilated cardiomyopathy, and progressive hepatic and renal failure. Patients present in childhood …
Alstrom syndrome is an autosomal recessive disease with multisystem involvement, including cone-rod dystrophy, hearing loss, type 2 diabetes …
Cannabinoids and the eye.
Wang MTM, Danesh-Meyer HV. Wang MTM, et al. Surv Ophthalmol. 2021 Mar-Apr;66(2):327-345. doi: 10.1016/j.survophthal.2020.07.002. Epub 2020 Aug 4. Surv Ophthalmol. 2021. PMID: 32763339 Review.
Neuro-ophthalmic associations include ocular motility deficits and decrements in smooth pursuit and saccadic eye movements, although potential therapeutic effects for congenital and acquired nystagmus have been observed....
Neuro-ophthalmic associations include ocular motility deficits and decrements in smooth pursuit and saccadic eye movements, although potenti …
Treatment of Nystagmus.
Thurtell MJ. Thurtell MJ. Semin Neurol. 2015 Oct;35(5):522-6. doi: 10.1055/s-0035-1563575. Epub 2015 Oct 6. Semin Neurol. 2015. PMID: 26444397 Review.
Acquired and congenital forms of nystagmus are commonly encountered in the course of clinical practice. ...The approach must be tailored depending on the type of nystagmus, its characteristics, and in some cases, its cause. In this review, the treatment appro …
Acquired and congenital forms of nystagmus are commonly encountered in the course of clinical practice. ...The approach must b …
Nystagmus.
Gottlob I. Gottlob I. Curr Opin Ophthalmol. 2001 Oct;12(5):378-83. doi: 10.1097/00055735-200110000-00010. Curr Opin Ophthalmol. 2001. PMID: 11588502 Review.
This article reviews the recent literature on nystagmus and various aspects of the pathophysiology of congenital idiopathic nystagmus and nystagmus treatment. ...Important contributions have been made to the genetics of various forms of nystagmus …
This article reviews the recent literature on nystagmus and various aspects of the pathophysiology of congenital idiopathic …
Nystagmus.
Neely DE, Sprunger DT. Neely DE, et al. Curr Opin Ophthalmol. 1999 Oct;10(5):320-6. doi: 10.1097/00055735-199910000-00007. Curr Opin Ophthalmol. 1999. PMID: 10621545 Review.
Nystagmus continues to be a complex subject of study. Our ability to characterize nystagmus has improved, but our comprehension of the oculomotor control process underlying this condition remains vague. We review recent advances in the characterization, classificati …
Nystagmus continues to be a complex subject of study. Our ability to characterize nystagmus has improved, but our comprehensio …
205 results