- Mutations in RD3 are associated with an extremely rare and severe form of early onset retinal dystrophy EOSRD.
Preising MN, Hausotter-Will N, Solbach MC, Friedburg C, Ruschendorf F, Lorenz B.
Invest Opthalmol Vis Sci 2012 Jun 8;53(7):3463-3472
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- Automated segmentation of retinal blood vessels in spectral domain optical coherence tomography scans.
Pilch M, Wenner W, Strohmayr E, Preising MN, Friedburg C, Meyer zu Bexten E, Lorenz B, Stieger K.
Biomed Opt Express. 2012 Jul 1;3(7):1478-91
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- Chromatic pupillometry dissects function of the three light sensitive retinal cell populations in RPE65 deficiency.
Lorenz B, Strohmayr E, Zahn S, Friedburg C, Kramer M, Preising MN, Stieger K.
Invest Ophthalmol Vis Sci 2012 July 53(9):5641-5652
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- Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.
Audo I, Bujakowska K, Orhan E, Poloschek CM, Defoort-Dhellemmes S, Drumare I, Kohl S, Luu TD, Lecompte O, Zrenner E, Lancelot ME, Antonio A, Germain A, Michiels C, Audier C, Letexier M, Saraiva JP, Leroy BP, Munier FL, Mohand-Saïd S, Lorenz B, Friedburg C, Preising M, Kellner U, Renner AB, Moskova-Doumanova V, Berger W, Wissinger B, Hamel CP, Schorderet DF, De Baere E, Sharon D, Banin E, Jacobson SG, Bonneau D, Zanlonghi X, Le Meur G, Casteels I, Koenekoop R, Long VW, Meire F, Prescott K, de Ravel TJ, Simmons I, Nguyen H, Dollfus H, Poch O, Léveillard T, Nguyen-Ba-Charvet K, Sahel JA, Bhattacharya SS, Zeitz C.
Am J Hum Genet. 2012 Feb 10;90(2):321-30.
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- Häufige Pupillenstörungen
Gräf M.
Z. prakt. Augenheilkd. 33:106-110
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- Beidseitige medialis-Rücklagerung mit Fadenoperation bei großer
frühkindlicher Esotropie
Gräf M, Gerlach T, Getmann O, Lorenz B.
Klin Monbl Augenheilk 2012; 229(10):987-994
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- How to deal with diplopia?
Gräf M, Lorenz B.
Revue Neurologique 168(10):720-728
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- Heritability of strabismus: genetic influence is specitif to eso-deviation
and independent of refractive error
Sanfilippo PG, Hammond CJ, Staffieri SE, Kearns LS, Melissa Liew SH,
Barbour JM, Hewitt AW, Ge D, Snieder H, Mackinnon JR, Brown SA,
Lorenz B, Spector TD, Martin NG, Wilmer JB, Mackey DA.
Twin Research and Human Genetics 15(5):624-630
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