Rosenberg T - Search Results

1

Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy.

Rosenberg T, Roos B, Johnsen T, Bech N, Scheetz TE, Larsen M, Stone EM, Fingert JH. Rosenberg T, et al. Mol Vis. 2010 Dec 9;16:2659-68. Mol Vis. 2010. PMID: 21179233 Free PMC article.

2

North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13.

Small KW, DeLuca AP, Whitmore SS, Rosenberg T, Silva-Garcia R, Udar N, Puech B, Garcia CA, Rice TA, Fishman GA, Héon E, Folk JC, Streb LM, Haas CM, Wiley LA, Scheetz TE, Fingert JH, Mullins RF, Tucker BA, Stone EM. Small KW, et al. Among authors: rosenberg t. Ophthalmology. 2016 Jan;123(1):9-18. doi: 10.1016/j.ophtha.2015.10.006. Epub 2015 Oct 24. Ophthalmology. 2016. PMID: 26507665 Free PMC article.

3

Oligocone trichromacy: clinical and molecular genetic investigations.

Andersen MK, Christoffersen NL, Sander B, Edmund C, Larsen M, Grau T, Wissinger B, Kohl S, Rosenberg T. Andersen MK, et al. Among authors: rosenberg t. Invest Ophthalmol Vis Sci. 2010 Jan;51(1):89-95. doi: 10.1167/iovs.09-3988. Epub 2009 Sep 24. Invest Ophthalmol Vis Sci. 2010. PMID: 19797231

4

Prevalence and diagnostic spectrum of generalized retinal dystrophy in Danish children.

Bertelsen M, Jensen H, Larsen M, Lorenz B, Preising MN, Rosenberg T. Bertelsen M, et al. Among authors: rosenberg t. Ophthalmic Epidemiol. 2013 Jun;20(3):164-9. doi: 10.3109/09286586.2013.776692. Epub 2013 May 10. Ophthalmic Epidemiol. 2013. PMID: 23662838

5

Generalized choriocapillaris dystrophy, a distinct phenotype in the spectrum of ABCA4-associated retinopathies.

Bertelsen M, Zernant J, Larsen M, Duno M, Allikmets R, Rosenberg T. Bertelsen M, et al. Among authors: rosenberg t. Invest Ophthalmol Vis Sci. 2014 Apr 29;55(4):2766-76. doi: 10.1167/iovs.13-13391. Invest Ophthalmol Vis Sci. 2014. PMID: 24713488 Free PMC article.

6

Lack of autofluorescence in fundus albipunctatus associated with mutations in RDH5.

Schatz P, Preising M, Lorenz B, Sander B, Larsen M, Eckstein C, Rosenberg T. Schatz P, et al. Among authors: rosenberg t. Retina. 2010 Nov-Dec;30(10):1704-13. doi: 10.1097/IAE.0b013e3181dc050a. Retina. 2010. PMID: 20829743

7

Fundus albipunctatus associated with compound heterozygous mutations in RPE65.

Schatz P, Preising M, Lorenz B, Sander B, Larsen M, Rosenberg T. Schatz P, et al. Among authors: rosenberg t. Ophthalmology. 2011 May;118(5):888-94. doi: 10.1016/j.ophtha.2010.09.005. Epub 2011 Jan 6. Ophthalmology. 2011. PMID: 21211845

8

[New treatments of hereditary blindness].

Bertelsen M, Rosenberg T, Larsen M. Bertelsen M, et al. Among authors: rosenberg t. Ugeskr Laeger. 2013 Sep 2;175(36):2038-42. Ugeskr Laeger. 2013. PMID: 23992912 Review. Danish.

9

Clinical Characteristics, Mutation Spectrum, and Prevalence of Åland Eye Disease/Incomplete Congenital Stationary Night Blindness in Denmark.

Hove MN, Kilic-Biyik KZ, Trotter A, Grønskov K, Sander B, Larsen M, Carroll J, Bech-Hansen T, Rosenberg T. Hove MN, et al. Among authors: rosenberg t. Invest Ophthalmol Vis Sci. 2016 Dec 1;57(15):6861-6869. doi: 10.1167/iovs.16-19445. Invest Ophthalmol Vis Sci. 2016. PMID: 28002560 Free PMC article.

10

Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.

Jespersgaard C, Fang M, Bertelsen M, Dang X, Jensen H, Chen Y, Bech N, Dai L, Rosenberg T, Zhang J, Møller LB, Tümer Z, Brøndum-Nielsen K, Grønskov K. Jespersgaard C, et al. Among authors: rosenberg t. Sci Rep. 2019 Feb 4;9(1):1219. doi: 10.1038/s41598-018-38007-2. Sci Rep. 2019. PMID: 30718709 Free PMC article.

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