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

2

A mutational hot spot in the mitochondrial ND6 gene in patients with Leber's hereditary optic neuropathy.

Luberichs J, Leo-Kottler B, Besch D, Fauser S. Luberichs J, et al. Among authors: besch d. Graefes Arch Clin Exp Ophthalmol. 2002 Feb;240(2):96-100. doi: 10.1007/s00417-001-0423-1. Graefes Arch Clin Exp Ophthalmol. 2002. PMID: 11931086

3

Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations.

Fauser S, Luberichs J, Besch D, Leo-Kottler B. Fauser S, et al. Among authors: besch d. Biochem Biophys Res Commun. 2002 Jul 12;295(2):342-7. doi: 10.1016/s0006-291x(02)00672-1. Biochem Biophys Res Commun. 2002. PMID: 12150954

4

Leber's hereditary optic neuropathy: clinical and molecular genetic results in a patient with a point mutation at np T11253C (isoleucine to threonine) in the ND4 gene and spontaneous recovery.

Leo-Kottler B, Luberichs J, Besch D, Christ-Adler M, Fauser S. Leo-Kottler B, et al. Among authors: besch d. Graefes Arch Clin Exp Ophthalmol. 2002 Sep;240(9):758-64. doi: 10.1007/s00417-002-0494-7. Epub 2002 Aug 2. Graefes Arch Clin Exp Ophthalmol. 2002. PMID: 12271374

5

Confirmation of the 14568 mutation in the mitochondrial ND6 gene as causative in Leber's hereditary optic neuropathy.

Fauser S, Leo-Kottler B, Besch D, Luberichs J. Fauser S, et al. Among authors: besch d. Ophthalmic Genet. 2002 Sep;23(3):191-7. doi: 10.1076/opge.23.3.191.7881. Ophthalmic Genet. 2002. PMID: 12324878

6

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: besch d. Biochem Biophys Res Commun. 1997 May 19;234(2):511-5. doi: 10.1006/bbrc.1997.6660. Biochem Biophys Res Commun. 1997. PMID: 9177303

7

[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. Ophthalmologe. 2000 Jan;97(1):22-6. doi: 10.1007/s003470050006. Ophthalmologe. 2000. PMID: 10663786 German.

8

Progressive cone dystrophy with deutan genotype and phenotype.

Scholl HP, Kremers J, Besch D, Zrenner E, Jägle H. Scholl HP, et al. Among authors: besch d. 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

9

Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa.

Schuster A, Weisschuh N, Jägle H, Besch D, Janecke AR, Zierler H, Tippmann S, Zrenner E, Wissinger B. Schuster A, et al. Among authors: besch d. Br J Ophthalmol. 2005 Oct;89(10):1258-64. doi: 10.1136/bjo.2004.063933. Br J Ophthalmol. 2005. PMID: 16170112 Free PMC article.

10

Safety evaluation of "retina implant alpha IMS"--a prospective clinical trial.

Kitiratschky VB, Stingl K, Wilhelm B, Peters T, Besch D, Sachs H, Gekeler F, Bartz-Schmidt KU, Zrenner E. Kitiratschky VB, et al. Among authors: besch d. Graefes Arch Clin Exp Ophthalmol. 2015 Mar;253(3):381-7. doi: 10.1007/s00417-014-2797-x. Epub 2014 Sep 16. Graefes Arch Clin Exp Ophthalmol. 2015. PMID: 25219982 Clinical Trial.

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