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[Ophthalmological screening studies in newborn infants. German Ophthalmological Society].
Clemens S, Eckardt C, Gerding H, Grote A, Jandeck C, Kellner U, Lorenz B, Petersen J, Seiberth V, Stärk N, Ulbig MW, Zubcov A, Jorch G, Pohlandt F. Clemens S, et al. Among authors: lorenz b. Ophthalmologe. 1999 Apr;96(4):257-63. doi: 10.1007/s003470050402. Ophthalmologe. 1999. PMID: 10409854 German. No abstract available.
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.
Kohl S, Varsanyi B, Antunes GA, Baumann B, Hoyng CB, Jägle H, Rosenberg T, Kellner U, Lorenz B, Salati R, Jurklies B, Farkas A, Andreasson S, Weleber RG, Jacobson SG, Rudolph G, Castellan C, Dollfus H, Legius E, Anastasi M, Bitoun P, Lev D, Sieving PA, Munier FL, Zrenner E, Sharpe LT, Cremers FP, Wissinger B. Kohl S, et al. Among authors: lorenz b. Eur J Hum Genet. 2005 Mar;13(3):302-8. doi: 10.1038/sj.ejhg.5201269. Eur J Hum Genet. 2005. PMID: 15657609
[Guidelines for ophthalmological screening of premature infants in Germany].
Jandeck C, Kellner U, Lorenz B, Seiberth V; Arbeitsgruppe der Retinologischen Gesellschaft zur Erstellung der Leitlinie zur augenärztlichen Screening-Untersuchung von Frühgeborenen. Jandeck C, et al. Among authors: lorenz b. Klin Monbl Augenheilkd. 2008 Feb;225(2):123-30. doi: 10.1055/s-2008-1027168. Klin Monbl Augenheilkd. 2008. PMID: 18293263 German.
[Acute retinopathy of prematurity].
Lorenz B. Lorenz B. Ophthalmologe. 2008 Dec;105(12):1090-1. doi: 10.1007/s00347-008-1786-z. Ophthalmologe. 2008. PMID: 19011870 German. No abstract available.
[Guidelines for ophthalmologic screening of premature infants].
Jandeck C, Kellner U, Lorenz B, Seiberth V. Jandeck C, et al. Among authors: lorenz b. Ophthalmologe. 2008 Oct;105(10):955-63. doi: 10.1007/s00347-008-1841-9. Ophthalmologe. 2008. PMID: 19224267 German. No abstract available.
502 results