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Page 1
Long-Term Follow-Up of a Family with Retinal Dystrophy Caused by RPE65 Mutation.
Case Rep Ophthalmol. 2023 Sep 19;14(1):454-461. doi: 10.1159/000530086. eCollection 2023 Jan-Dec.
Case Rep Ophthalmol. 2023.
PMID: 37901629
Free PMC article.
[Ophthalmologic manifestations of Bardet-Biedl syndrome].
Sohár N, Jánossy Á, Janáky M, Facskó A.
Sohár N, et al. Among authors: janossy a.
Orv Hetil. 2013 Dec 29;154(52):2071-7. doi: 10.1556/OH.2013.29748.
Orv Hetil. 2013.
PMID: 24374583
Hungarian.
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[Gene therapy treatment based on an ophthalmic indication in hereditary retinal dystrophy caused by RPE65 biallelic gene mutation.].
Vizvári E, Smeller L, Jánossy Á, Lőrincz M, Janáky M, Tóth-Molnár E.
Vizvári E, et al. Among authors: janossy a.
Orv Hetil. 2022 Nov 27;163(48):1923-1931. doi: 10.1556/650.2022.32636. Print 2022 Nov 27.
Orv Hetil. 2022.
PMID: 36436058
Hungarian.
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Immunohistochemical Analysis of a Vitreous Membrane Removed from a Patient with Incontinentia Pigmenti-Related Retinal Detachment.
Janáky M, Hári Kovács A, Jánossy Á, Török D, Ivanyi B, Braunitzer G, Benedek G.
Janáky M, et al. Among authors: janossy a.
Vision (Basel). 2020 Jan 2;4(1):5. doi: 10.3390/vision4010005.
Vision (Basel). 2020.
PMID: 31906444
Free PMC article.
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