PubMed for id: 377837

Year	Number of Results
2003	1
2006	3
2007	2
2008	15
2009	21
2010	31
2011	20
2012	32
2013	32
2014	44
2015	37
2016	37
2017	43
2018	40
2019	40
2020	42
2021	43
2022	48
2023	41
2024	12

1

Identification of copy number variation in the gene for autosomal dominant optic atrophy, OPA1, in a Chinese pedigree.

Jin X, Chen YH, Liu Z, Deng Y, Li NN, Huang H, Qi M, Yi X, Zhu J. Jin X, et al. Genet Mol Res. 2015 Sep 21;14(3):10961-72. doi: 10.4238/2015.September.21.8. Genet Mol Res. 2015. PMID: 26400325 Free article.

2

First cases of dominant optic atrophy in Saudi Arabia: report of two novel OPA1 mutations.

Galvez-Ruiz A, Neuhaus C, Bergmann C, Bolz H. Galvez-Ruiz A, et al. J Neuroophthalmol. 2013 Dec;33(4):349-53. doi: 10.1097/WNO.0b013e31829ffb9a. J Neuroophthalmol. 2013. PMID: 24051421

3

Dominant optic atrophy.

Lenaers G, Hamel C, Delettre C, Amati-Bonneau P, Procaccio V, Bonneau D, Reynier P, Milea D. Lenaers G, et al. Orphanet J Rare Dis. 2012 Jul 9;7:46. doi: 10.1186/1750-1172-7-46. Orphanet J Rare Dis. 2012. PMID: 22776096 Free PMC article. Review.

4

[Genetic basis of hereditary optic atrophies].

Wawrocka A, Krawczyński MR. Wawrocka A, et al. Klin Oczna. 2007;109(10-12):470-4. Klin Oczna. 2007. PMID: 18488399 Review. Polish.

5

Colonization and vertical transmission of Streptococcus mutans in Turkish children.

Hameş-Kocabaş EE, Uçar F, Kocataş Ersin N, Uzel A, Alpöz AR. Hameş-Kocabaş EE, et al. Microbiol Res. 2008;163(2):168-72. doi: 10.1016/j.micres.2006.03.016. Epub 2006 Jun 2. Microbiol Res. 2008. PMID: 16735109 Free article.

6

Structural model of the OPA1 GTPase domain may explain the molecular consequences of a novel mutation in a family with autosomal dominant optic atrophy.

Dadgar S, Hagens O, Dadgar SR, Haghighi EN, Schimpf S, Wissinger B, Garshasbi M. Dadgar S, et al. Exp Eye Res. 2006 Sep;83(3):702-6. doi: 10.1016/j.exer.2006.03.004. Epub 2006 May 12. Exp Eye Res. 2006. PMID: 16698014

7

Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.

Eiberg H, Hansen L, Kjer B, Hansen T, Pedersen O, Bille M, Rosenberg T, Tranebjaerg L. Eiberg H, et al. J Med Genet. 2006 May;43(5):435-40. doi: 10.1136/jmg.2005.034892. J Med Genet. 2006. PMID: 16648378 Free PMC article.

8

Antibody specificities and effect of meningococcal carriage in icelandic teenagers receiving the Norwegian serogroup B outer membrane vesicle vaccine.

Wedege E, Kuipers B, Bolstad K, van Dijken H, Frøholm LO, Vermont C, Caugant DA, van den Dobbelsteen G. Wedege E, et al. Infect Immun. 2003 Jul;71(7):3775-81. doi: 10.1128/IAI.71.7.3775-3781.2003. Infect Immun. 2003. PMID: 12819059 Free PMC article.

9

Therapeutic benefit of idebenone in patients with Leber hereditary optic neuropathy: The LEROS nonrandomized controlled trial.

Yu-Wai-Man P, Carelli V, Newman NJ, Silva MJ, Linden A, Van Stavern G, Szaflik JP, Banik R, Lubiński W, Pemp B, Liao YJ, Subramanian PS, Misiuk-Hojło M, Newman S, Castillo L, Kocięcki J, Levin MH, Muñoz-Negrete FJ, Yagan A, Cherninkova S, Katz D, Meunier A, Votruba M, Korwin M, Dziedziak J, Jurkutė N, Harvey JP, La Morgia C, Priglinger C, Llòria X, Tomasso L, Klopstock T; LEROS Study Group. Yu-Wai-Man P, et al. Cell Rep Med. 2024 Mar 19;5(3):101437. doi: 10.1016/j.xcrm.2024.101437. Epub 2024 Feb 29. Cell Rep Med. 2024. PMID: 38428428 Free PMC article. Clinical Trial.

10

Thiamine-Responsive Megaloblastic Anaemia With Hypothyroidism, A Puzzling Association.

Rai VR, Ibrahim MN, Javed MN, Khoso Z, Rathore H. Rai VR, et al. J Ayub Med Coll Abbottabad. 2023 Oct-Dec;35(Suppl 1)(4):S804-S806. doi: 10.55519/JAMC-S4-12486. J Ayub Med Coll Abbottabad. 2023. PMID: 38406914 Free article.

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