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Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European study.
Stingl K, Kurtenbach A, Hahn G, Kernstock C, Hipp S, Zobor D, Kohl S, Bonnet C, Mohand-Saïd S, Audo I, Fakin A, Hawlina M, Testa F, Simonelli F, Petit C, Sahel JA, Zrenner E. Stingl K, et al. Among authors: hawlina m. Doc Ophthalmol. 2019 Oct;139(2):151-160. doi: 10.1007/s10633-019-09704-8. Epub 2019 Jul 2. Doc Ophthalmol. 2019. PMID: 31267413
Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy.
Fakin A, Šuštar M, Brecelj J, Bonnet C, Petit C, Zupan A, Glavač D, Jarc-Vidmar M, Battelino S, Hawlina M. Fakin A, et al. Among authors: hawlina m. Genes (Basel). 2019 Nov 21;10(12):956. doi: 10.3390/genes10120956. Genes (Basel). 2019. PMID: 31766479 Free PMC article.
ISCEV standard for clinical pattern electroretinography--2007 update.
Holder GE, Brigell MG, Hawlina M, Meigen T, Vaegan, Bach M; International Society for Clinical Electrophysiology of Vision. Holder GE, et al. Among authors: hawlina m. Doc Ophthalmol. 2007 May;114(3):111-6. doi: 10.1007/s10633-007-9053-1. Epub 2007 Apr 14. Doc Ophthalmol. 2007. PMID: 17435967 Free PMC article.
Phenotypic variation in enhanced S-cone syndrome.
Audo I, Michaelides M, Robson AG, Hawlina M, Vaclavik V, Sandbach JM, Neveu MM, Hogg CR, Hunt DM, Moore AT, Bird AC, Webster AR, Holder GE. Audo I, et al. Among authors: hawlina m. Invest Ophthalmol Vis Sci. 2008 May;49(5):2082-93. doi: 10.1167/iovs.05-1629. Invest Ophthalmol Vis Sci. 2008. PMID: 18436841
Genotyping microarray (gene chip) for the ABCR (ABCA4) gene.
Jaakson K, Zernant J, Külm M, Hutchinson A, Tonisson N, Glavac D, Ravnik-Glavac M, Hawlina M, Meltzer MR, Caruso RC, Testa F, Maugeri A, Hoyng CB, Gouras P, Simonelli F, Lewis RA, Lupski JR, Cremers FP, Allikmets R. Jaakson K, et al. Among authors: hawlina m. Hum Mutat. 2003 Nov;22(5):395-403. doi: 10.1002/humu.10263. Hum Mutat. 2003. PMID: 14517951
120 results