Leo-Kottler B - Search Results

1

Encephalopathic Susac's Syndrome associated with livedo racemosa in a young woman before the completion of family planning.

Engeholm M, Leo-Kottler B, Rempp H, Lindig T, Lerche H, Kleffner I, Henes M, Dihné M. Engeholm M, et al. Among authors: leo kottler b. BMC Neurol. 2013 Nov 25;13:185. doi: 10.1186/1471-2377-13-185. BMC Neurol. 2013. PMID: 24274741 Free PMC article.

2

[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.

3

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

4

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

5

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

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. 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

[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. Ophthalmologe. 1995 Feb;92(1):86-92. Ophthalmologe. 1995. PMID: 7719084 German.

8

Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy.

Achilli A, Iommarini L, Olivieri A, Pala M, Hooshiar Kashani B, Reynier P, La Morgia C, Valentino ML, Liguori R, Pizza F, Barboni P, Sadun F, De Negri AM, Zeviani M, Dollfus H, Moulignier A, Ducos G, Orssaud C, Bonneau D, Procaccio V, Leo-Kottler B, Fauser S, Wissinger B, Amati-Bonneau P, Torroni A, Carelli V. Achilli A, et al. Among authors: leo kottler b. PLoS One. 2012;7(8):e42242. doi: 10.1371/journal.pone.0042242. Epub 2012 Aug 3. PLoS One. 2012. PMID: 22879922 Free PMC article.

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

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

32 results

Search Page

Filters