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

Year Number of Results
1975 1
1977 1
1985 1
1988 1
1991 1
1994 1
1995 1
1998 2
1999 1
2001 1
2003 1
2004 1
2005 1
2006 2
2007 2
2008 2
2009 1
2010 1
2011 3
2012 5
2013 3
2014 2
2015 1
2016 3
2017 2
2018 5
2019 4
2020 3
2021 3
2022 3
2023 3
2024 1

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55 results

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Page 1
Coats disease: An overview of classification, management and outcomes.
Sen M, Shields CL, Honavar SG, Shields JA. Sen M, et al. Indian J Ophthalmol. 2019 Jun;67(6):763-771. doi: 10.4103/ijo.IJO_841_19. Indian J Ophthalmol. 2019. PMID: 31124484 Free PMC article. Review.
Coats disease is an idiopathic retinal vascular disorder with retinal telangiectasia with intraretinal and/or subretinal exudation without appreciable retinal or vitreal traction. ...Over the years, we have shifted from enucleation to a more conservative appr …
Coats disease is an idiopathic retinal vascular disorder with retinal telangiectasia with intraretinal and/or subretinal exuda …
Recent advances in the diagnosis and treatment of Coats' disease.
Yang X, Wang C, Su G. Yang X, et al. Int Ophthalmol. 2019 Apr;39(4):957-970. doi: 10.1007/s10792-019-01095-8. Epub 2019 Mar 20. Int Ophthalmol. 2019. PMID: 30895419 Review.
RESULTS: Coats' disease is characterized by idiopathic leaky retinal vascular telangiectasia and microvascular abnormalities often accompanied by intraretinal or subretinal exudation and retinal detachment. ...Coats' disease has significant diversity i …
RESULTS: Coats' disease is characterized by idiopathic leaky retinal vascular telangiectasia and microvascular abnormalities o …
Familial Exudative Vitreoretinopathy: Pathophysiology, Diagnosis, and Management.
Tauqeer Z, Yonekawa Y. Tauqeer Z, et al. Asia Pac J Ophthalmol (Phila). 2018 May-Jun;7(3):176-182. doi: 10.22608/APO.201855. Epub 2018 Apr 9. Asia Pac J Ophthalmol (Phila). 2018. PMID: 29633588 Free article. Review.
This in turn can cause further pathological changes including neovascularization, exudation, hemorrhage, and retinal detachment. The biological basis of the disease is thought to be from defects in the Wnt signaling pathway. ...The current treatment paradigm …
This in turn can cause further pathological changes including neovascularization, exudation, hemorrhage, and retinal detachment
Foveal photoreceptor disruption in ocular diseases: An optical coherence tomography-based differential diagnosis.
Singh SR, Vaidya H, Borrelli E, Chhablani J. Singh SR, et al. Surv Ophthalmol. 2023 Jul-Aug;68(4):655-668. doi: 10.1016/j.survophthal.2023.03.003. Epub 2023 Mar 18. Surv Ophthalmol. 2023. PMID: 36934831 Review.
Focal photoreceptor disruption usually involves loss or rarefaction of ellipsoid/interdigitation zone, either in isolation or associated with external limiting membrane or retinal pigment epithelium disruption in the fovea. Vitreomacular interface (VMI) disorders including …
Focal photoreceptor disruption usually involves loss or rarefaction of ellipsoid/interdigitation zone, either in isolation or associated wit …
Occult globe rupture: diagnostic and treatment challenge.
Chronopoulos A, Ong JM, Thumann G, Schutz JS. Chronopoulos A, et al. Surv Ophthalmol. 2018 Sep-Oct;63(5):694-699. doi: 10.1016/j.survophthal.2018.04.001. Epub 2018 Apr 9. Surv Ophthalmol. 2018. PMID: 29649485 Review.
Occult globe rupture is a traumatic dehiscence of the sclera at or posterior to the rectus muscle insertions without a visible eye wall defect on slit lamp examination. Occult scleral ruptures are important because they can be difficult to diagnose, but normally require pr …
Occult globe rupture is a traumatic dehiscence of the sclera at or posterior to the rectus muscle insertions without a visible eye wall d
The use of emergency apheresis in the management of plasma cell disorders.
Kalayoglu-Besisik S. Kalayoglu-Besisik S. Transfus Apher Sci. 2018 Feb;57(1):35-39. doi: 10.1016/j.transci.2018.02.014. Epub 2018 Feb 20. Transfus Apher Sci. 2018. PMID: 29477943 Review.
The most commonly used replacement fluid is 4%-5% human albumin in physiologic saline. FFP may be used in patients with coagulation abnormalities. Plasmapheresis should be continued until acute symptoms abate. Hyperviscosity impairs the circulation in the retina and causes …
The most commonly used replacement fluid is 4%-5% human albumin in physiologic saline. FFP may be used in patients with coagulation abnor
Retinopathy of Prematurity: Pathogenesis and Current Treatment Options.
Quimson SK. Quimson SK. Neonatal Netw. 2015;34(5):284-7. doi: 10.1891/0730-0832.34.5.284. Neonatal Netw. 2015. PMID: 26802829 Review.
Retinopathy of prematurity (ROP) is a vasoproliferative retinal disorder that continues to be the major cause of preventable childhood blindness worldwide. ...Approximately 65 percent of neonates with <1,250 g birth weight and 80 percent of those with 1,000 g birth weig …
Retinopathy of prematurity (ROP) is a vasoproliferative retinal disorder that continues to be the major cause of preventable childhoo …
A Review of DNA and Histone Methylation Alterations in the New Era of Diagnosis and Treatment of Retinal Diseases.
Rasoulinejad SA, Maroufi F. Rasoulinejad SA, et al. Curr Mol Med. 2021;21(8):607-619. doi: 10.2174/1566524020666201209103603. Curr Mol Med. 2021. PMID: 33297915 Review.
Here, we reviewed the DNA and histone methylation alterations in common retinal diseases, focusing on agerelated macular degeneration (AMD), diabetic retinopathy, retinal detachment (RD), retinitis pigmentosa, retinal aging, and retinoblastoma. Then we …
Here, we reviewed the DNA and histone methylation alterations in common retinal diseases, focusing on agerelated macular degeneration …
Redesigning services for the management of vitreomacular traction and macular hole.
Amoaku W, Cackett P, Tyagi A, Mahmood U, Nosek J, Mennie G, Rumney N. Amoaku W, et al. Eye (Lond). 2014 Jul;28 Suppl 1(Suppl 1):S1-10. doi: 10.1038/eye.2014.125. Eye (Lond). 2014. PMID: 25008433 Free PMC article. Review.
However, ocriplasmin has demonstrated favourable efficacy and safety in specific patient groups with VMT/MH and is now recommended as a treatment option for certain patients by the National Institute of Health and Care Excellence. This means that services for managing pati …
However, ocriplasmin has demonstrated favourable efficacy and safety in specific patient groups with VMT/MH and is now recommended as a trea …
Genetic testing results of children suspected to have Stickler syndrome type collagenopathy after ocular examination.
Khan AO, AlAbdi L, Patel N, Helaby R, Hashem M, Abdulwahab F, AlBadr FB, Alkuraya FS. Khan AO, et al. Mol Genet Genomic Med. 2021 May;9(5):e1628. doi: 10.1002/mgg3.1628. Epub 2021 May 5. Mol Genet Genomic Med. 2021. PMID: 33951325 Free PMC article.
METHODS: Retrospective consecutive case series (2014-2016) of children (<12 years old) suspected to have Stickler syndrome type collagenopathy by a single ophthalmologist and able to complete genetic testing for this possibility. Suspicion was based on vitreous abnormalitie
METHODS: Retrospective consecutive case series (2014-2016) of children (<12 years old) suspected to have Stickler syndrome type collageno …
55 results