Wissinger B - Search Results

1

Spatial and temporal resolution of the photoreceptors rescue dynamics after treatment with voretigene neparvovec.

Stingl K, Kempf M, Bartz-Schmidt KU, Dimopoulos S, Reichel F, Jung R, Kelbsch C, Kohl S, Kortüm FC, Nasser F, Peters T, Wilhelm B, Wissinger B, Wozar F, Zrenner E, Fischer MD, Stingl K. Stingl K, et al. Among authors: wissinger b. Br J Ophthalmol. 2022 Jun;106(6):831-838. doi: 10.1136/bjophthalmol-2020-318286. Epub 2021 Jan 20. Br J Ophthalmol. 2022. PMID: 33472769 Free PMC article.

2

Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.

Leo-Kottler B, Christ-Adler M, Baumann B, Zrenner E, Wissinger B. Leo-Kottler B, et al. Among authors: wissinger b. Ger J Ophthalmol. 1996 Jul;5(4):233-40. Ger J Ophthalmol. 1996. PMID: 8854108

3

Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of cases.

Weber BH, Sander S, Kopp C, Walker D, Eckstein A, Wissinger B, Zrenner E, Grimm T. Weber BH, et al. Among authors: wissinger b. Br J Ophthalmol. 1996 Aug;80(8):745-9. doi: 10.1136/bjo.80.8.745. Br J Ophthalmol. 1996. PMID: 8949721 Free PMC article.

4

RDS/peripherin gene mutations are frequent causes of central retinal dystrophies.

Kohl S, Christ-Adler M, Apfelstedt-Sylla E, Kellner U, Eckstein A, Zrenner E, Wissinger B. Kohl S, et al. Among authors: wissinger b. J Med Genet. 1997 Aug;34(8):620-6. doi: 10.1136/jmg.34.8.620. J Med Genet. 1997. PMID: 9279751 Free PMC article.

5

Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel.

Kohl S, Marx T, Giddings I, Jägle H, Jacobson SG, Apfelstedt-Sylla E, Zrenner E, Sharpe LT, Wissinger B. Kohl S, et al. Among authors: wissinger b. Nat Genet. 1998 Jul;19(3):257-9. doi: 10.1038/935. Nat Genet. 1998. PMID: 9662398

6

[Diagnostic error in Leber's optic neuropathy. Value of clinical and molecular genetic studies].

Leo-Kottler B, Christ-Adler M, Wissinger B, Zrenner E. Leo-Kottler B, et al. Among authors: wissinger b. Ophthalmologe. 1998 Aug;95(8):549-54. doi: 10.1007/s003470050314. Ophthalmologe. 1998. PMID: 9782731 German.

7

The role of the peripherin/RDS gene in retinal dystrophies.

Kohl S, Giddings I, Besch D, Apfelstedt-Sylla E, Zrenner E, Wissinger B. Kohl S, et al. Among authors: wissinger b. Acta Anat (Basel). 1998;162(2-3):75-84. doi: 10.1159/000046471. Acta Anat (Basel). 1998. PMID: 9831753 Review.

8

Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis.

Seeliger MW, Biesalski HK, Wissinger B, Gollnick H, Gielen S, Frank J, Beck S, Zrenner E. Seeliger MW, et al. Among authors: wissinger b. Invest Ophthalmol Vis Sci. 1999 Jan;40(1):3-11. Invest Ophthalmol Vis Sci. 1999. PMID: 9888420

9

Direct visual resolution of gene copy number in the human photopigment gene array.

Wolf S, Sharpe LT, Schmidt HJ, Knau H, Weitz S, Kioschis P, Poustka A, Zrenner E, Lichter P, Wissinger B. Wolf S, et al. Among authors: wissinger b. Invest Ophthalmol Vis Sci. 1999 Jun;40(7):1585-9. Invest Ophthalmol Vis Sci. 1999. PMID: 10359341

10

Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene.

Besch D, Leo-Kottler B, Zrenner E, Wissinger B. Besch D, et al. Among authors: wissinger b. Graefes Arch Clin Exp Ophthalmol. 1999 Sep;237(9):745-52. doi: 10.1007/s004170050307. Graefes Arch Clin Exp Ophthalmol. 1999. PMID: 10447650

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