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

Year Number of Results
1991 1
1992 1
1993 1
1995 2
1996 2
1997 1
1999 1
2000 2
2001 1
2003 1
2010 2
2011 1
2012 1
2013 1
2015 2
2016 3
2017 3
2018 5
2019 2
2021 4
2022 3
2023 2
2024 0

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36 results

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Page 1
Posterior keratoconus.
Silas MR, Hilkert SM, Reidy JJ, Farooq AV. Silas MR, et al. Br J Ophthalmol. 2018 Jul;102(7):863-867. doi: 10.1136/bjophthalmol-2017-311097. Epub 2017 Nov 9. Br J Ophthalmol. 2018. PMID: 29122822 Review.
Posterior keratoconus (PKC) is a rare, typically non-inflammatory condition that is characterised by an abnormal posterior corneal curvature, which may be accompanied by overlying stromal opacification. It is usually congenital and can be associated with other ocular and s …
Posterior keratoconus (PKC) is a rare, typically non-inflammatory condition that is characterised by an abnormal posterior corneal curvature …
Anterior segment dysgenesis: Insights into the genetics and pathogenesis.
Kaushik S, Dubey S, Choudhary S, Ratna R, Pandav SS, Khan AO. Kaushik S, et al. Indian J Ophthalmol. 2022 Jul;70(7):2293-2303. doi: 10.4103/ijo.IJO_3223_21. Indian J Ophthalmol. 2022. PMID: 35791109 Free PMC article. Review.
The fundamental pathophysiology of all childhood glaucoma is impaired outflow through the trabecular meshwork. Anterior segment Dysgeneses (ASD) are a group of non-acquired ocular anomalies associated with glaucoma, characterized by developmental abnormalities
The fundamental pathophysiology of all childhood glaucoma is impaired outflow through the trabecular meshwork. Anterior segment
FOXE3 mutations: genotype-phenotype correlations.
Plaisancié J, Ragge NK, Dollfus H, Kaplan J, Lehalle D, Francannet C, Morin G, Colineaux H, Calvas P, Chassaing N. Plaisancié J, et al. Clin Genet. 2018 Apr;93(4):837-845. doi: 10.1111/cge.13177. Clin Genet. 2018. PMID: 29136273 Review.
Among these, is the FOXE3 gene, which was initially described in individuals with dominantly inherited anterior segment dysgenesis and, subsequently, associated with recessively inherited primary aphakia, sclerocornea and microphthalmia. In this work, we desc …
Among these, is the FOXE3 gene, which was initially described in individuals with dominantly inherited anterior segment dys
Relationship between neural crest cell specification and rare ocular diseases.
Akula M, Park JW, West-Mays JA. Akula M, et al. J Neurosci Res. 2019 Jan;97(1):7-15. doi: 10.1002/jnr.24245. Epub 2018 Apr 16. J Neurosci Res. 2019. PMID: 29660784 Free PMC article. Review.
The POM is comprised of neural crest-derived mesenchymal progenitor cells that give rise to numerous important ocular structures including those tissues that form the optic cup and anterior segment of the eye. A number of genes are involved in the migration and spec …
The POM is comprised of neural crest-derived mesenchymal progenitor cells that give rise to numerous important ocular structures including t …
Systematic review and meta-analysis of congenitally missing permanent dentition: Sex dimorphism, occurrence patterns, associated factors and biasing factors.
Rakhshan V, Rakhshan A. Rakhshan V, et al. Int Orthod. 2016 Sep;14(3):273-94. doi: 10.1016/j.ortho.2016.07.016. Epub 2016 Aug 10. Int Orthod. 2016. PMID: 27522615 Review.
RESULTS: Seventy-four studies were included. The mean CMT prevalence was 6.422.76% in males and 7.552.67% in females. Overall, CMT is more prevalent in females but only in epidemiological samples, and not in orthodontic or dental patients. ...There is not a significant pre …
RESULTS: Seventy-four studies were included. The mean CMT prevalence was 6.422.76% in males and 7.552.67% in females. Overall, CMT is …
Clinical and molecular aspects of congenital aniridia - A review of current concepts.
Tibrewal S, Ratna R, Gour A, Agarkar S, Dubey S, Ganesh S, Kekunnaya R, Sangwan V, Liu Y, Vanita V. Tibrewal S, et al. Indian J Ophthalmol. 2022 Jul;70(7):2280-2292. doi: 10.4103/ijo.IJO_2255_21. Indian J Ophthalmol. 2022. PMID: 35791108 Free PMC article. Review.
Congenital aniridia is a pan ocular disorder characterized by partial or total loss of iris tissue as the defining feature. ...Recently, aniridia-like phenotypes have been reported due to non-PAX6 mutations as in PITX2, FOXC1, FOXD3, TRIM44, and CYP1B1 as well wherein ther
Congenital aniridia is a pan ocular disorder characterized by partial or total loss of iris tissue as the defining feature. ...Recent
A comparative approach to anterior segment dysgenesis.
Williams DL. Williams DL. Eye (Lond). 1993;7 ( Pt 5):607-16. doi: 10.1038/eye.1993.142. Eye (Lond). 1993. PMID: 8287980 Review.
The role of animal models in our developing understanding of anterior segment dysgenesis is outlined. Research in avian models shows the importance of the neural crest in the development of the anterior segment and the failure of terms such as …
The role of animal models in our developing understanding of anterior segment dysgenesis is outlined. Research in avian …
Abandoning the Supraorbital Bandeau in Anterior Craniosynostosis Repairs, for a Single-Segment Reconstruction.
Fearon JA, Ditthakasem K, Garcia JC, Herbert M. Fearon JA, et al. Plast Reconstr Surg. 2018 Sep;142(3):334e-341e. doi: 10.1097/PRS.0000000000004649. Plast Reconstr Surg. 2018. PMID: 30148778 Review.
BACKGROUND: Following correction of anterior sutural fusions, long-term forehead irregularities may arise. ...The purpose of this review was to compare outcomes and complications between children who underwent reconstruction with the traditional supraorbital bandeau and th …
BACKGROUND: Following correction of anterior sutural fusions, long-term forehead irregularities may arise. ...The purpose of this rev …
Red reflex test screening for neonates: A systematic review and meta analysis.
Taksande A, Jameel PZ, Taksande B, Meshram R. Taksande A, et al. Indian J Ophthalmol. 2021 Aug;69(8):1994-2003. doi: 10.4103/ijo.IJO_3632_20. Indian J Ophthalmol. 2021. PMID: 34304165 Free PMC article. Review.
The purpose was this review was to systematically evaluate the diagnostic accuracy of RRT for the detection of ocular abnormalities in newborns. PubMed, EMBASE, Scopus, Web of Science, and Cochrane database of systematic reviews were the data sources. ...The results of our …
The purpose was this review was to systematically evaluate the diagnostic accuracy of RRT for the detection of ocular abnormalities i …
Genetics of aniridia and anterior segment dysgenesis.
Churchill A, Booth A. Churchill A, et al. Br J Ophthalmol. 1996 Jul;80(7):669-73. doi: 10.1136/bjo.80.7.669. Br J Ophthalmol. 1996. PMID: 8795384 Free PMC article. Review. No abstract available.
36 results