Leo-Kottler B - Search Results

1

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. 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

2

Genomic rearrangements in OPA1 are frequent in patients with autosomal dominant optic atrophy.

Fuhrmann N, Alavi MV, Bitoun P, Woernle S, Auburger G, Leo-Kottler B, Yu-Wai-Man P, Chinnery P, Wissinger B. Fuhrmann N, et al. Among authors: leo kottler b. J Med Genet. 2009 Feb;46(2):136-44. doi: 10.1136/jmg.2008.062570. J Med Genet. 2009. PMID: 19181907

3

OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance.

Pesch UE, Leo-Kottler B, Mayer S, Jurklies B, Kellner U, Apfelstedt-Sylla E, Zrenner E, Alexander C, Wissinger B. Pesch UE, et al. Hum Mol Genet. 2001 Jun 15;10(13):1359-68. doi: 10.1093/hmg/10.13.1359. Hum Mol Genet. 2001. PMID: 11440988

4

Ocular symptoms in association with antiphospholipid antibodies.

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

5

[Leber's hereditary optic neuropathy].

Leo-Kottler B, Wissinger B. Leo-Kottler B, et al. Ophthalmologe. 2011 Dec;108(12):1179-92; quiz 1193-4. doi: 10.1007/s00347-011-2482-y. Ophthalmologe. 2011. PMID: 22130685 German.

6

[How to distinguish between autosomal dominant optic atrophy and Leber's hereditary optic neuropathy].

Leo-Kottler B, Jägle H, Küpker T, Schimpf S. Leo-Kottler B, et al. Ophthalmologe. 2007 Dec;104(12):1060-5. doi: 10.1007/s00347-007-1577-y. Ophthalmologe. 2007. PMID: 17899121 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. Invest Ophthalmol Vis Sci. 2001 May;42(6):1208-14. Invest Ophthalmol Vis Sci. 2001. PMID: 11328729

8

[Leber optic neuropathy with clinical improvement].

Leo-Kottler B, Jacobi F, Christ-Adler M. Leo-Kottler B, et al. Ophthalmologe. 2000 Dec;97(12):849-54. doi: 10.1007/s003470070007. Ophthalmologe. 2000. PMID: 11227157 German.

9

[Leber optic neuropathy in women and children].

Leo-Kottler B, Christ-Adler M. Leo-Kottler B, et al. Ophthalmologe. 1999 Nov;96(11):698-701. doi: 10.1007/s003470050479. Ophthalmologe. 1999. PMID: 10631830 German.

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. 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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