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Diagnostic genome sequencing improves diagnostic yield: a prospective single-centre study in 1000 patients with inherited eye diseases.
Weisschuh N, Mazzola P, Zuleger T, Schaeferhoff K, Kühlewein L, Kortüm F, Witt D, Liebmann A, Falb R, Pohl L, Reith M, Stühn LG, Bertrand M, Müller A, Casadei N, Kelemen O, Kelbsch C, Kernstock C, Richter P, Sadler F, Demidov G, Schütz L, Admard J, Sturm M, Grasshoff U, Tonagel F, Heinrich T, Nasser F, Wissinger B, Ossowski S, Kohl S, Riess O, Stingl K, Haack TB. Weisschuh N, et al. Among authors: nasser f. J Med Genet. 2024 Jan 19;61(2):186-195. doi: 10.1136/jmg-2023-109470. J Med Genet. 2024. PMID: 37734845 Free PMC article.
Fixation Location and Stability Using the MP-1 Microperimeter in Stargardt Disease: ProgStar Report No. 3.
Schönbach EM, Ibrahim MA, Strauss RW, Birch DG, Cideciyan AV, Hahn GA, Ho A, Kong X, Nasser F, Sunness JS, Zrenner E, Sadda SR, West SK, Scholl HPN; Progression of Stargardt Disease Study Group. Schönbach EM, et al. Among authors: nasser f. Ophthalmol Retina. 2017 Jan-Feb;1(1):68-76. doi: 10.1016/j.oret.2016.08.009. Epub 2016 Oct 31. Ophthalmol Retina. 2017. PMID: 31047397
FUNDUS ALBIPUNCTATUS ASSOCIATED WITH CONE DYSFUNCTION.
Kuehlewein L, Nasser F, Gloeckle N, Kohl S, Zrenner E. Kuehlewein L, et al. Among authors: nasser f. Retin Cases Brief Rep. 2017 Winter;11 Suppl 1:S73-S76. doi: 10.1097/ICB.0000000000000420. Retin Cases Brief Rep. 2017. PMID: 27627638
A case of X-linked retinoschisis with atypical fundus appearance.
Nasser F, Kohl S, Kuehlewein L, Wissinger B, Obermaier CD, Kurtenbach A, Zrenner E. Nasser F, et al. Doc Ophthalmol. 2019 Aug;139(1):75-81. doi: 10.1007/s10633-019-09698-3. Epub 2019 Apr 20. Doc Ophthalmol. 2019. PMID: 31006083
151 results