Kellner U - Search Results

1

[Screening for retinopathy of prematurity-the most important changes in the new German guidelines 2020].

Li JQ, Kellner U, Lorenz B, Stahl A, Krohne TU. Li JQ, et al. Among authors: kellner u. Ophthalmologe. 2021 Dec;118(12):1240-1244. doi: 10.1007/s00347-021-01393-6. Epub 2021 Apr 30. Ophthalmologe. 2021. PMID: 33931789 Free PMC article. Review. German.

2

[Evaluation of published recommendations for screening studies of retinopathy of prematurity].

Kellner U, Jandeck C, Helbig H, Versmold H, Bossi E, Körner F, Foerster MH. Kellner U, et al. Ophthalmologe. 1995 Oct;92(5):681-4. Ophthalmologe. 1995. PMID: 8750996 German.

3

[Limits and possibilities of vitreous body surgery in diabetic retinopathy].

Helbig H, Kellner U, Bornfeld N, Foerster MH. Helbig H, et al. Among authors: kellner u. Ophthalmologe. 1996 Dec;93(6):647-54. doi: 10.1007/s003470050052. Ophthalmologe. 1996. PMID: 9081518 German.

4

[Long-term vision follow-up after vitrectomy in diabetic retinopathy].

Helbig H, Kellner U, Bornfeld N, Foerster MH. Helbig H, et al. Among authors: kellner u. Ophthalmologe. 1997 Apr;94(4):268-72. doi: 10.1007/s003470050111. Ophthalmologe. 1997. PMID: 9229494 German.

5

[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: kellner u. Ophthalmologe. 1999 Apr;96(4):257-63. doi: 10.1007/s003470050402. Ophthalmologe. 1999. PMID: 10409854 German. No abstract available.

6

[Ocular changes in premature infants].

Jandeck C, Kellner U, Foerster MH. Jandeck C, et al. Among authors: kellner u. Ophthalmologe. 2000 Nov;97(11):799-818. doi: 10.1007/s003470070033. Ophthalmologe. 2000. PMID: 11130173 German. No abstract available.

7

Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsia.

Kohl S, Baumann B, Rosenberg T, Kellner U, Lorenz B, Vadalà M, Jacobson SG, Wissinger B. Kohl S, et al. Among authors: kellner u. Am J Hum Genet. 2002 Aug;71(2):422-5. doi: 10.1086/341835. Epub 2002 Jun 20. Am J Hum Genet. 2002. PMID: 12077706 Free PMC article.

8

[Retinopathy of prematurity].

Jandeck C, Kellner U, Foerster MH. Jandeck C, et al. Among authors: kellner u. Klin Monbl Augenheilkd. 2004 Mar;221(3):147-59. doi: 10.1055/s-2004-812886. Klin Monbl Augenheilkd. 2004. PMID: 15052520 Review. German.

9

[Comparison of the anatomical and functional outcome after laser or cryotherapy for retinopathy of prematurity (ROP)].

Jandeck C, Kellner U, Heimann H, Foerster MH. Jandeck C, et al. Among authors: kellner u. Ophthalmologe. 2005 Jan;102(1):33-8. doi: 10.1007/s00347-004-1049-6. Ophthalmologe. 2005. PMID: 15221254 German.

10

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: kellner u. Eur J Hum Genet. 2005 Mar;13(3):302-8. doi: 10.1038/sj.ejhg.5201269. Eur J Hum Genet. 2005. PMID: 15657609

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