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Year Number of Results
1988 1
1992 1
1994 1
1995 2
1996 1
1998 1
2000 3
2003 3
2004 1
2005 1
2009 1
2010 1
2011 2
2012 3
2013 2
2015 1
2016 6
2017 3
2018 3
2019 4
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2021 9
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2023 4
2024 3
2025 0

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56 results

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Page 1
Immune responses to injury and their links to eye disease.
Stepp MA, Menko AS. Stepp MA, et al. Transl Res. 2021 Oct;236:52-71. doi: 10.1016/j.trsl.2021.05.005. Epub 2021 May 27. Transl Res. 2021. PMID: 34051364 Free PMC article. Review.
As a result, many regions of the eye evolved mechanisms to deliver immune cells to sites of dysgenesis, injury, or in response to the many age-related pathologies. While the purpose of these immune responses is reparative or protective, cytokines released by immune cells c …
As a result, many regions of the eye evolved mechanisms to deliver immune cells to sites of dysgenesis, injury, or in response to the …
Axenfeld-Rieger syndrome.
Seifi M, Walter MA. Seifi M, et al. Clin Genet. 2018 Jun;93(6):1123-1130. doi: 10.1111/cge.13148. Epub 2018 Jan 25. Clin Genet. 2018. PMID: 28972279 Review.
Axenfeld-Rieger syndrome (ARS) is a clinically and genetically heterogeneous group of developmental disorders affecting primarily the anterior segment of the eye, often leading to secondary glaucoma. Patients with ARS may also present with systemic changes, includin …
Axenfeld-Rieger syndrome (ARS) is a clinically and genetically heterogeneous group of developmental disorders affecting primarily the ant
Ring chromosome 6 in a child with anterior segment dysgenesis and review of its overlap with other FOXC1 deletion phenotypes.
Corona-Rivera JR, Corona-Rivera A, Zepeda-Romero LC, Rios-Flores IM, Rivera-Vargas J, Orozco-Vela M, Santana-Bejarano UF, Torres-Anguiano E, Pinto-Cardoso M, David D, Bobadilla-Morales L. Corona-Rivera JR, et al. Congenit Anom (Kyoto). 2019 Sep;59(5):174-178. doi: 10.1111/cga.12309. Epub 2018 Oct 9. Congenit Anom (Kyoto). 2019. PMID: 30225942 Review.
Here, we report a patient with ring chromosome 6 [r(6)], associated with anterior segment dysgenesis (ASD) and other anomalies. The phenotype was due to a 1880 kb microdeletion at 6p25.3 identified by whole-genome array analysis, and was mainly …
Here, we report a patient with ring chromosome 6 [r(6)], associated with anterior segment dysgenesis (ASD …
Update on pediatric corneal diseases and keratoplasty.
Vanathi M, Raj N, Kusumesh R, Aron N, Gupta N, Tandon R. Vanathi M, et al. Surv Ophthalmol. 2022 Nov-Dec;67(6):1647-1684. doi: 10.1016/j.survophthal.2022.07.010. Epub 2022 Jul 30. Surv Ophthalmol. 2022. PMID: 35918016 Review.
Advancements in the genetic basis of congenital corneal diseases and investigations in congenital corneal conditions provide a better understanding of pediatric corneal conditions. ...Graft rejection, graft infection, amblyopia, and glaucoma continue to be serious c …
Advancements in the genetic basis of congenital corneal diseases and investigations in congenital corneal conditions provide a …
Axenfeld-Rieger syndrome: a novel histopathologic finding associated with corneal abnormalities.
Yu T, Dai Z, Peng R, Xiao G, Zhang P, Ma S, Hong J. Yu T, et al. BMC Ophthalmol. 2022 Dec 28;22(1):514. doi: 10.1186/s12886-022-02754-8. BMC Ophthalmol. 2022. PMID: 36577962 Free PMC article. Review.
BACKGROUND: Axenfeld-Rieger syndrome (ARS) is a rare kind of anterior segment dysgenesis (ASD). The most common ocular features of ARS are posterior embryotoxon and iris hypoplasia, while some patients may manifest as corneal opacity and edema. ...CONCLUSION: …
BACKGROUND: Axenfeld-Rieger syndrome (ARS) is a rare kind of anterior segment dysgenesis (ASD). The most common ocular …
Ultrasound biomicroscopy of the anterior segment in patients with primary congenital glaucoma: a review of the literature.
Janssens R, van Rijn LJ, Eggink CA, Jansonius NM, Janssen SF. Janssens R, et al. Acta Ophthalmol. 2022 Sep;100(6):605-613. doi: 10.1111/aos.15082. Epub 2021 Dec 22. Acta Ophthalmol. 2022. PMID: 34939345 Free article. Review.
PURPOSE: Primary congenital glaucoma (PCG) is a form of childhood glaucoma caused by maldevelopment of the anterior chamber. ...The success rate of glaucoma surgery depended on the severity of anterior segment malformations found with UBM. CONCLUSION: …
PURPOSE: Primary congenital glaucoma (PCG) is a form of childhood glaucoma caused by maldevelopment of the anterior chamber. . …
A comprehensive review of the anterior fontanelle: embryology, anatomy, and clinical considerations.
D'Antoni AV, Donaldson OI, Schmidt C, Macchi V, De Caro R, Oskouian RJ, Loukas M, Shane Tubbs R. D'Antoni AV, et al. Childs Nerv Syst. 2017 Jun;33(6):909-914. doi: 10.1007/s00381-017-3406-1. Epub 2017 Apr 10. Childs Nerv Syst. 2017. PMID: 28396968 Review.
METHODS: Using a standard database search, we conducted a review of the anterior fontanelle, including its embryology, anatomy, pathology, and related surgical implications. CONCLUSIONS: The diagnostic value of the anterior fontanelle, through observation of its sha …
METHODS: Using a standard database search, we conducted a review of the anterior fontanelle, including its embryology, anatomy, patho …
[Glaucoma Surgery in Anterior Segment Dysgeneses].
van Oterendorp C. van Oterendorp C. Klin Monbl Augenheilkd. 2019 Jun;236(6):745-750. doi: 10.1055/a-0839-9091. Epub 2019 May 2. Klin Monbl Augenheilkd. 2019. PMID: 31049915 Review. German.
Anterior segment dysgeneses are rare conditions, and mostly occur sporadically. The severity of dysgenesis and the number of structures affected are highly variable. Glaucoma occurs in approximately 50% of all patients, either as part of primary chamber angle
Anterior segment dysgeneses are rare conditions, and mostly occur sporadically. The severity of dysgenesis and the numb
Zika virus and the eye.
de Paula Freitas B, Ventura CV, Maia M, Belfort R Jr. de Paula Freitas B, et al. Curr Opin Ophthalmol. 2017 Nov;28(6):595-599. doi: 10.1097/ICU.0000000000000420. Curr Opin Ophthalmol. 2017. PMID: 28795959 Review.
Five fundus patterns were seen most often: macular chorioretinal atrophy, chorioretinal atrophy elsewhere, focal pigmentary changes in the macular region, optic nerve abnormalities and combined types. A few studies have suggested that the ZIKV might damage the anterior
Five fundus patterns were seen most often: macular chorioretinal atrophy, chorioretinal atrophy elsewhere, focal pigmentary changes in the m …
The phenotypic spectrum of terminal and subterminal 6p deletions based on a social media-derived cohort and literature review.
Rraku E, Kerstjens-Frederikse WS, Swertz MA, Dijkhuizen T, van Ravenswaaij-Arts CMA, Engwerda A. Rraku E, et al. Orphanet J Rare Dis. 2023 Mar 24;18(1):68. doi: 10.1186/s13023-023-02670-0. Orphanet J Rare Dis. 2023. PMID: 36964621 Free PMC article. Review.
BACKGROUND: Terminal 6p deletions are rare, and information on their clinical consequences is scarce, which impedes optimal management and follow-up by clinicians. The parent-driven Chromosome 6 Project collaborates with families of affected children worldwide to better un …
BACKGROUND: Terminal 6p deletions are rare, and information on their clinical consequences is scarce, which impedes optimal management and f …
56 results