Fiebig BS - Search Results

1

Phenotypic variability and long-term follow-up of patients with known and novel PRPH2/RDS gene mutations.

Renner AB, Fiebig BS, Weber BH, Wissinger B, Andreasson S, Gal A, Cropp E, Kohl S, Kellner U. Renner AB, et al. Among authors: fiebig bs. Am J Ophthalmol. 2009 Mar;147(3):518-530.e1. doi: 10.1016/j.ajo.2008.09.007. Epub 2008 Nov 26. Am J Ophthalmol. 2009. PMID: 19038374

2

Progression of retinal pigment epithelial alterations during long-term follow-up in female carriers of choroideremia and report of a novel CHM mutation.

Renner AB, Fiebig BS, Cropp E, Weber BH, Kellner U. Renner AB, et al. Among authors: fiebig bs. Arch Ophthalmol. 2009 Jul;127(7):907-12. doi: 10.1001/archophthalmol.2009.123. Arch Ophthalmol. 2009. PMID: 19597113

3

ERG variability in X-linked congenital retinoschisis patients with mutations in the RS1 gene and the diagnostic importance of fundus autofluorescence and OCT.

Renner AB, Kellner U, Fiebig B, Cropp E, Foerster MH, Weber BH. Renner AB, et al. Doc Ophthalmol. 2008 Mar;116(2):97-109. doi: 10.1007/s10633-007-9094-5. Epub 2007 Nov 7. Doc Ophthalmol. 2008. PMID: 17987333

4

Gyrate atrophy: clinical and genetic findings in a female without arginine-restricted diet during her first 39 years of life and report of a new OAT gene mutation.

Renner AB, Walter A, Fiebig BS, Jägle H. Renner AB, et al. Among authors: fiebig bs. Doc Ophthalmol. 2012 Aug;125(1):81-9. doi: 10.1007/s10633-012-9335-0. Epub 2012 Jun 7. Doc Ophthalmol. 2012. PMID: 22674428

5

Lipofuscin- and melanin-related fundus autofluorescence in patients with ABCA4-associated retinal dystrophies.

Kellner S, Kellner U, Weber BH, Fiebig B, Weinitz S, Ruether K. Kellner S, et al. Am J Ophthalmol. 2009 May;147(5):895-902, 902.e1. doi: 10.1016/j.ajo.2008.12.023. Epub 2009 Feb 25. Am J Ophthalmol. 2009. PMID: 19243736

6

Fundus Autofluorescence and SD-OCT Document Rapid Progression in Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Associated with a c.256G > A Mutation in BEST1.

Kellner S, Stöhr H, Fiebig B, Weinitz S, Farmand G, Kellner U, Weber BH. Kellner S, et al. Ophthalmic Genet. 2016 Jun;37(2):201-8. doi: 10.3109/13816810.2015.1033556. Epub 2016 Jan 15. Ophthalmic Genet. 2016. PMID: 26771239

7

[Evidence-based diagnostic approach to inherited retinal dystrophies 2009].

Kellner U, Kellner S, Renner AB, Fiebig BS, Weinitz S, Weber BH. Kellner U, et al. Among authors: fiebig bs. Klin Monbl Augenheilkd. 2009 Dec;226(12):999-1011. doi: 10.1055/s-0028-1109684. Epub 2009 Sep 15. Klin Monbl Augenheilkd. 2009. PMID: 19757352 Review. German.

8

A subgroup of age-related macular degeneration is associated with mono-allelic sequence variants in the ABCA4 gene.

Fritsche LG, Fleckenstein M, Fiebig BS, Schmitz-Valckenberg S, Bindewald-Wittich A, Keilhauer CN, Renner AB, Mackensen F, Mößner A, Pauleikhoff D, Adrion C, Mansmann U, Scholl HP, Holz FG, Weber BH. Fritsche LG, et al. Among authors: fiebig bs. Invest Ophthalmol Vis Sci. 2012 Apr 30;53(4):2112-8. doi: 10.1167/iovs.11-8785. Invest Ophthalmol Vis Sci. 2012. PMID: 22427542

9

Lipofuscin- and melanin-related fundus autofluorescence visualize different retinal pigment epithelial alterations in patients with retinitis pigmentosa.

Kellner U, Kellner S, Weber BH, Fiebig B, Weinitz S, Ruether K. Kellner U, et al. Eye (Lond). 2009 Jun;23(6):1349-59. doi: 10.1038/eye.2008.280. Epub 2008 Sep 12. Eye (Lond). 2009. PMID: 18791550

10

Gross rearrangements in BRCA1 but not BRCA2 play a notable role in predisposition to breast and ovarian cancer in high-risk families of German origin.

Preisler-Adams S, Schönbuchner I, Fiebig B, Welling B, Dworniczak B, Weber BH. Preisler-Adams S, et al. Cancer Genet Cytogenet. 2006 Jul 1;168(1):44-9. doi: 10.1016/j.cancergencyto.2005.07.005. Cancer Genet Cytogenet. 2006. PMID: 16772120

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