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

Year Number of Results
1975 1
1976 1
1981 2
1984 2
1986 1
1989 1
1990 2
1991 3
1993 1
1994 1
1995 1
1996 2
1997 3
1998 1
1999 7
2000 1
2001 2
2002 3
2003 5
2004 2
2005 1
2006 3
2007 2
2008 6
2009 5
2010 3
2011 1
2012 6
2013 4
2014 7
2015 3
2016 5
2017 12
2018 6
2019 3
2020 7
2021 2
2022 4
2023 4
2024 1

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112 results

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Page 1
Normal and abnormal foveal development.
Thomas MG, Papageorgiou E, Kuht HJ, Gottlob I. Thomas MG, et al. Br J Ophthalmol. 2022 May;106(5):593-599. doi: 10.1136/bjophthalmol-2020-316348. Epub 2020 Nov 4. Br J Ophthalmol. 2022. PMID: 33148537 Review.
The outer segment thickness is a surrogate marker for cone density and in foveal hypoplasia this correlates strongly with visual acuity. In preverbal children grading FH can help predict future visual acuity....
The outer segment thickness is a surrogate marker for cone density and in foveal hypoplasia this correlates strongly with visual acuity. In …
Superior segmental optic nerve hypoplasia: A review.
Wu JH, Lin CW, Liu CH, Weinreb RN, Welsbie DS. Wu JH, et al. Surv Ophthalmol. 2022 Sep-Oct;67(5):1467-1475. doi: 10.1016/j.survophthal.2022.02.008. Epub 2022 Feb 18. Surv Ophthalmol. 2022. PMID: 35189184 Review.
Optical coherence tomography can be helpful in distinguishing SSONH by demonstrating superonasal retinal nerve fiber layer thinning, as compared to the inferotemporal thinning seen in glaucoma, and an aberrant extension of retinal pigment epithelium over Bruch membrane. Overall, …
Optical coherence tomography can be helpful in distinguishing SSONH by demonstrating superonasal retinal nerve fiber layer thinning, as comp …
Childhood blindness.
Steinkuller PG, Du L, Gilbert C, Foster A, Collins ML, Coats DK. Steinkuller PG, et al. J AAPOS. 1999 Feb;3(1):26-32. doi: 10.1016/s1091-8531(99)70091-1. J AAPOS. 1999. PMID: 10071898
Optic Nerve Hypoplasia and Crouzon Syndrome.
Eves D, O'Connor SJ, Boyle MA. Eves D, et al. J Pediatr Ophthalmol Strabismus. 2018 Dec 19;55:e45-e48. doi: 10.3928/01913913-20181012-02. J Pediatr Ophthalmol Strabismus. 2018. PMID: 30571838
Genetic testing confirmed a molecular diagnosis of Crouzon syndrome. He had a complicated course in relation to choanal stenosis management, and was discharged home at 10 weeks of age. ...
Genetic testing confirmed a molecular diagnosis of Crouzon syndrome. He had a complicated course in relation to choanal stenosis mana …
Reappraisal of the optic nerve hypoplasia syndrome.
Borchert M. Borchert M. J Neuroophthalmol. 2012 Mar;32(1):58-67. doi: 10.1097/WNO.0b013e31824442b8. J Neuroophthalmol. 2012. PMID: 22330852 Review.
Other common neuroradiographic associations, such as corpus callosum hypoplasia, gyrus dysplasia, and cortical heterotopia, may have prognostic significance. CONCLUSIONS: Children with ONH need to be monitored for many systemic, developmental, and even life-threatening pro …
Other common neuroradiographic associations, such as corpus callosum hypoplasia, gyrus dysplasia, and cortical heterotopia, may have prog …
Neuroimaging and endocrine disorders in paediatric optic nerve hypoplasia.
Qian X, Fouzdar Jain S, Morgan LA, Kruse T, Cabrera M, Suh DW. Qian X, et al. Br J Ophthalmol. 2018 Jul;102(7):906-910. doi: 10.1136/bjophthalmol-2017-310763. Epub 2017 Oct 5. Br J Ophthalmol. 2018. PMID: 28982953
CONCLUSION: This study has determined that abnormal MRI findings do not have the sensitivity to predict endocrinopathy, nor does a normal MRI rule out possible endocrine abnormalities. ...
CONCLUSION: This study has determined that abnormal MRI findings do not have the sensitivity to predict endocrinopathy, nor does a no …
Optic nerve hypoplasia: a review.
Ouvrier R, Billson F. Ouvrier R, et al. J Child Neurol. 1986 Jul;1(3):181-8. doi: 10.1177/088307388600100302. J Child Neurol. 1986. PMID: 3298397 Review.
Precocious puberty and hypogonadism have also been observed. The prognosis of optic nerve hypoplasia depends upon the severity of the changes in the optic nerves and especially the degree of associated cerebral malformation. ...
Precocious puberty and hypogonadism have also been observed. The prognosis of optic nerve hypoplasia depends upon the severity of the …
Congenital anomalies of the optic disc: insights from optical coherence tomography imaging.
Jeng-Miller KW, Cestari DM, Gaier ED. Jeng-Miller KW, et al. Curr Opin Ophthalmol. 2017 Nov;28(6):579-586. doi: 10.1097/ICU.0000000000000425. Curr Opin Ophthalmol. 2017. PMID: 28817389 Review.
Further study employing OCT to elucidate structure-function relationships of congenital optic nerve anomalies will help expand the role of OCT in clinical practice related to diagnosis, prognosis, and management of these entities....
Further study employing OCT to elucidate structure-function relationships of congenital optic nerve anomalies will help expand the role of O …
Use of sweep visual evoked potential in preverbal children with optic nerve hypoplasia.
Bradfield YS, Ver Hoeve JN, Aul B, Struck MC. Bradfield YS, et al. J AAPOS. 2022 Jun;26(3):131.e1-131.e6. doi: 10.1016/j.jaapos.2022.01.012. Epub 2022 May 13. J AAPOS. 2022. PMID: 35577018
Sweep VEP, and the combination of ONH severity and neurologic status, were significant predictors (P < 0.05) of logMAR optotype acuity, together accounting for 54%-61% of the variance in final recognition acuity. ...

Sweep VEP, and the combination of ONH severity and neurologic status, were significant predictors (P < 0.05) of logMAR optotype ac

…
Brain Malformations Do Not Predict Hypopituitarism in Young Children with Optic Nerve Hypoplasia.
Garcia-Filion P, Almarzouki H, Fink C, Geffner M, Nelson M, Borchert M. Garcia-Filion P, et al. Horm Res Paediatr. 2017;88(3-4):251-257. doi: 10.1159/000479029. Epub 2017 Aug 22. Horm Res Paediatr. 2017. PMID: 28848142 Free PMC article.
No association was noted for absent septum pellucidum (38%; p = 0.073), corpus callosum abnormality (51%; p = 0.625), and major malformations (22%; p = 0.407). A malformation conferred a positive predictive value of 71% (95% CI: 62%, 80%), and a negative predictive …
No association was noted for absent septum pellucidum (38%; p = 0.073), corpus callosum abnormality (51%; p = 0.625), and major malformation …
112 results