Similar articles for PMID: 20417568

Year	Number of Results
2001	2
2002	3
2003	5
2004	1
2005	3
2006	4
2007	7
2008	7
2009	5
2010	11
2011	12
2012	6
2013	9
2014	7
2015	9
2016	10
2017	13
2018	9
2019	6
2020	7
2021	12
2022	14
2023	2
2024	0

1

OPA1 mutations associated with dominant optic atrophy influence optic nerve head size.

Barboni P, Carbonelli M, Savini G, Foscarini B, Parisi V, Valentino ML, Carta A, De Negri A, Sadun F, Zeviani M, Sadun AA, Schimpf S, Wissinger B, Carelli V. Barboni P, et al. Ophthalmology. 2010 Aug;117(8):1547-53. doi: 10.1016/j.ophtha.2009.12.042. Epub 2010 Apr 24. Ophthalmology. 2010. PMID: 20417568

2

Retinal nerve fiber layer thickness in dominant optic atrophy measurements by optical coherence tomography and correlation with age.

Barboni P, Savini G, Parisi V, Carbonelli M, La Morgia C, Maresca A, Sadun F, De Negri AM, Carta A, Sadun AA, Carelli V. Barboni P, et al. Ophthalmology. 2011 Oct;118(10):2076-80. doi: 10.1016/j.ophtha.2011.02.027. Epub 2011 May 31. Ophthalmology. 2011. PMID: 21621262

3

The prevalence and natural history of dominant optic atrophy due to OPA1 mutations.

Yu-Wai-Man P, Griffiths PG, Burke A, Sellar PW, Clarke MP, Gnanaraj L, Ah-Kine D, Hudson G, Czermin B, Taylor RW, Horvath R, Chinnery PF. Yu-Wai-Man P, et al. Ophthalmology. 2010 Aug;117(8):1538-46, 1546.e1. doi: 10.1016/j.ophtha.2009.12.038. Epub 2010 Apr 24. Ophthalmology. 2010. PMID: 20417570 Free PMC article.

4

Genetic screening for OPA1 and OPA3 mutations in patients with suspected inherited optic neuropathies.

Yu-Wai-Man P, Shankar SP, Biousse V, Miller NR, Bean LJ, Coffee B, Hegde M, Newman NJ. Yu-Wai-Man P, et al. Ophthalmology. 2011 Mar;118(3):558-63. doi: 10.1016/j.ophtha.2010.07.029. Epub 2010 Oct 30. Ophthalmology. 2011. PMID: 21036400 Free PMC article.

5

Pattern of retinal ganglion cell loss in dominant optic atrophy due to OPA1 mutations.

Yu-Wai-Man P, Bailie M, Atawan A, Chinnery PF, Griffiths PG. Yu-Wai-Man P, et al. Eye (Lond). 2011 May;25(5):596-602. doi: 10.1038/eye.2011.2. Epub 2011 Mar 4. Eye (Lond). 2011. PMID: 21378995 Free PMC article.

6

Heterozygous deletion of the OPA1 gene in patients with dominant optic atrophy.

Hayashi T, Sasano H, Katagiri S, Tsunoda K, Kameya S, Nakazawa M, Iwata T, Tsuneoka H. Hayashi T, et al. Jpn J Ophthalmol. 2017 Sep;61(5):395-401. doi: 10.1007/s10384-017-0522-0. Epub 2017 Jul 1. Jpn J Ophthalmol. 2017. PMID: 28668999

7

Early macular retinal ganglion cell loss in dominant optic atrophy: genotype-phenotype correlation.

Barboni P, Savini G, Cascavilla ML, Caporali L, Milesi J, Borrelli E, La Morgia C, Valentino ML, Triolo G, Lembo A, Carta A, De Negri A, Sadun F, Rizzo G, Parisi V, Pierro L, Bianchi Marzoli S, Zeviani M, Sadun AA, Bandello F, Carelli V. Barboni P, et al. Am J Ophthalmol. 2014 Sep;158(3):628-36.e3. doi: 10.1016/j.ajo.2014.05.034. Epub 2014 Jun 5. Am J Ophthalmol. 2014. PMID: 24907432

8

Autosomal dominant optic atrophy with OPA1 gene mutations accompanied by auditory neuropathy and other systemic complications in a Japanese cohort.

Maeda-Katahira A, Nakamura N, Hayashi T, Katagiri S, Shimizu S, Ohde H, Matsunaga T, Kaga K, Nakano T, Kameya S, Matsuura T, Fujinami K, Iwata T, Tsunoda K. Maeda-Katahira A, et al. Mol Vis. 2019 Oct 5;25:559-573. eCollection 2019. Mol Vis. 2019. PMID: 31673222 Free PMC article.

9

Dominant optic atrophy: correlation between clinical and molecular genetic studies.

Puomila A, Huoponen K, Mäntyjärvi M, Hämäläinen P, Paananen R, Sankila EM, Savontaus ML, Somer M, Nikoskelainen E. Puomila A, et al. Acta Ophthalmol Scand. 2005 Jun;83(3):337-46. doi: 10.1111/j.1600-0420.2005.00448.x. Acta Ophthalmol Scand. 2005. PMID: 15948788 Free article.

10

Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy.

Chen Y, Jia X, Wang P, Xiao X, Li S, Guo X, Zhang Q. Chen Y, et al. Mol Vis. 2013;19:292-302. Epub 2013 Feb 6. Mol Vis. 2013. PMID: 23401657 Free PMC article.

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