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Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye.
JAMA. 2021 Feb 23;325(8):753-764. doi: 10.1001/jama.2021.0507.
JAMA. 2021.
PMID: 33620406
Free PMC article.
Twenty-four-hour intraocular pressure monitoring in normotensive patients undergoing chronic hemodialysis.
Panagiotou ES, Liakopoulos V, Giannopoulos T, Voudouragkaki IC, Demirtzi P, Paschalinou E, Nikitidou O, Kapis PV, Konstas AG.
Panagiotou ES, et al.
Eur J Ophthalmol. 2016 Jan-Feb;26(1):24-9. doi: 10.5301/ejo.5000651. Epub 2015 Jul 8.
Eur J Ophthalmol. 2016.
PMID: 26165324
Clinical Trial.
Item in Clipboard
How Successful is Switching from Bevacizumab or Ranibizumab to Aflibercept in Age-Related Macular Degeneration? A Systematic Overview.
Empeslidis T, Storey M, Giannopoulos T, Konidaris V, Tranos PG, Panagiotou ES, Voudouragkaki IC, Konstas AG.
Empeslidis T, et al. Among authors: panagiotou es.
Adv Ther. 2019 Jul;36(7):1532-1548. doi: 10.1007/s12325-019-00971-0. Epub 2019 May 17.
Adv Ther. 2019.
PMID: 31102206
Free PMC article.
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Management of Full-Thickness Macular Hole in A Genetically Confirmed Case with Usher Syndrome.
Panagiotou ES, Papathomas T, Nikopoulos K, Koukoula S, Quinodoz M, Rehman AU, Giannopoulos T, Rivolta C, Konstas AG.
Panagiotou ES, et al.
Ophthalmol Ther. 2020 Sep;9(3):677-684. doi: 10.1007/s40123-020-00276-4. Epub 2020 Jun 21.
Ophthalmol Ther. 2020.
PMID: 32566994
Free PMC article.
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Preservative-free tafluprost/timolol fixed combination: comparative 24-h efficacy administered morning or evening in open-angle glaucoma patients.
Konstas AG, Katsanos A, Athanasopoulos GP, Voudouragkaki IC, Panagiotou ES, Pagkalidou E, Haidich AB, Giannoulis DA, Spathi E, Giannopoulos T, Katz LJ.
Konstas AG, et al. Among authors: panagiotou es.
Expert Opin Pharmacother. 2018 Dec;19(18):1981-1988. doi: 10.1080/14656566.2018.1534958. Epub 2018 Oct 17.
Expert Opin Pharmacother. 2018.
PMID: 30328725
Clinical Trial.
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Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia.
Panagiotou ES, Fernandez-Fuentes N, Farraj LA, McKibbin M, Elçioglu NH, Jafri H, Cerman E, Parry DA, Logan CV, Johnson CA, Inglehearn CF, Toomes C, Ali M.
Panagiotou ES, et al.
Mol Vis. 2022 May 17;28:57-69. eCollection 2022.
Mol Vis. 2022.
PMID: 35693420
Free PMC article.
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Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani origin.
Ravesh Z, El Asrag ME, Weisschuh N, McKibbin M, Reuter P, Watson CM, Baumann B, Poulter JA, Sajid S, Panagiotou ES, O'Sullivan J, Abdelhamed Z, Bonin M, Soltanifar M, Black GC, Amin-ud Din M, Toomes C, Ansar M, Inglehearn CF, Wissinger B, Ali M.
Ravesh Z, et al. Among authors: panagiotou es.
Mol Vis. 2015 Mar 7;21:236-43. eCollection 2015.
Mol Vis. 2015.
PMID: 25802487
Free PMC article.
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Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
Panagiotou ES, Sanjurjo Soriano C, Poulter JA, Lord EC, Dzulova D, Kondo H, Hiyoshi A, Chung BH, Chu YW, Lai CHY, Tafoya ME, Karjosukarso D, Collin RWJ, Topping J, Downey LM, Ali M, Inglehearn CF, Toomes C.
Panagiotou ES, et al.
Am J Hum Genet. 2017 Jun 1;100(6):960-968. doi: 10.1016/j.ajhg.2017.05.001.
Am J Hum Genet. 2017.
PMID: 28575650
Free PMC article.
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