Zrenner E - Search Results

1

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: zrenner e. Graefes Arch Clin Exp Ophthalmol. 1999 Sep;237(9):745-52. doi: 10.1007/s004170050307. Graefes Arch Clin Exp Ophthalmol. 1999. PMID: 10447650

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: zrenner e. Ger J Ophthalmol. 1996 Jul;5(4):233-40. Ger J Ophthalmol. 1996. PMID: 8854108

3

Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathy.

Wissinger B, Besch D, Baumann B, Fauser S, Christ-Adler M, Jurklies B, Zrenner E, Leo-Kottler B. Wissinger B, et al. Among authors: zrenner e. Biochem Biophys Res Commun. 1997 May 19;234(2):511-5. doi: 10.1006/bbrc.1997.6660. Biochem Biophys Res Commun. 1997. PMID: 9177303

4

Ocular symptoms in association with antiphospholipid antibodies.

Leo-Kottler B, Klein R, Berg PA, Zrenner E. Leo-Kottler B, et al. Among authors: zrenner e. Graefes Arch Clin Exp Ophthalmol. 1998 Sep;236(9):658-68. doi: 10.1007/s004170050138. Graefes Arch Clin Exp Ophthalmol. 1998. PMID: 9782426

5

[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: zrenner e. Ophthalmologe. 1998 Aug;95(8):549-54. doi: 10.1007/s003470050314. Ophthalmologe. 1998. PMID: 9782731 German.

6

[A case of Leber optic neuropathy with a new point mutation in the cytochrome b gene].

Besch D, Wissinger B, Zrenner E, Leo-Kotter B. Besch D, et al. Among authors: zrenner e. Ophthalmologe. 2000 Jan;97(1):22-6. doi: 10.1007/s003470050006. Ophthalmologe. 2000. PMID: 10663786 German.

7

Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy.

Jacobi FK, Leo-Kottler B, Mittelviefhaus K, Zrenner E, Meyer J, Pusch CM, Wissinger B. Jacobi FK, et al. Among authors: zrenner e. Invest Ophthalmol Vis Sci. 2001 May;42(6):1208-14. Invest Ophthalmol Vis Sci. 2001. PMID: 11328729

8

[Correlation between clinical and molecular genetic findings in Leber's optic atrophy].

Leo-Kottler B, Christ-Adler M, Reck B, Wissinger B, Zrenner E. Leo-Kottler B, et al. Among authors: zrenner e. Ophthalmologe. 1995 Feb;92(1):86-92. Ophthalmologe. 1995. PMID: 7719084 German.

9

Inner retinal contributions to the multifocal electroretinogram: patients with Leber's hereditary optic neuropathy (LHON). Multifocal ERG in patients with LHON.

Kurtenbach A, Leo-Kottler B, Zrenner E. Kurtenbach A, et al. Among authors: zrenner e. Doc Ophthalmol. 2004 May;108(3):231-40. doi: 10.1007/s10633-004-8676-8. Doc Ophthalmol. 2004. PMID: 15573947

10

Progressive cone dystrophy with deutan genotype and phenotype.

Scholl HP, Kremers J, Besch D, Zrenner E, Jägle H. Scholl HP, et al. Among authors: zrenner e. Graefes Arch Clin Exp Ophthalmol. 2006 Feb;244(2):183-91. doi: 10.1007/s00417-005-0022-7. Epub 2005 Aug 5. Graefes Arch Clin Exp Ophthalmol. 2006. PMID: 16082559

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