Advanced search
Publication Cover
Ophthalmic Genetics Volume 23, 2002 - Issue 1
Submit an article Journal homepage
35
Views
14
CrossRef citations to date
0
Altmetric
Research Article

Progressive autosomal dominant optic atrophy and sensorineural hearing loss in a Turkish family

Serap Özden Departments of Ophthalmology,
,
Füsun Düzcan Departments of Medical Biology,
,
Bernd Wollnik Departments of Division of Medical Genetics, Institute of Child Health, Istanbul University, Istanbul, Turkey
,
G. Ozan Çetin Departments of Medical Biology,
,
Türker Sahiner Departments of Neurology,
,
Ismet Bayramoglu Departments of Otorhinolaringology, Medical Faculty, Pamukkale University, Denizli, and
,
Memnune Yüksel-Apak Departments of Division of Medical Genetics, Institute of Child Health, Istanbul University, Istanbul, Turkey
&
Hüseyin Bagci Departments of Medical Biology,
 show all
Pages 29-36 | Published online: 08 Jul 2009

Citations (14)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (1)

Golge Acaroglu, Yasemin Alanay, Pascal Reynier, Patrizia Amati-Bonneau & Gamze Men. (2005) Clinical Heterogeneity of Hereditary Optic Atrophy in a Turkish Family. Neuro-Ophthalmology 29:1, pages 9-15.
Read now

Articles from other publishers (13)

Michael C. BrodskyMichael C. Brodsky. 2016. Pediatric Neuro-Ophthalmology. Pediatric Neuro-Ophthalmology 199 274 .
Michelle Y. Wang, Alfredo A. Sadun & Jane W. Chan. 2014. Optic Nerve Disorders. Optic Nerve Disorders 209 248 .
Michael C. BrodskyMichael C. Brodsky. 2010. Pediatric Neuro-Ophthalmology. Pediatric Neuro-Ophthalmology 155 211 .
Will Yarosh, Jessica Monserrate, James Jiayuan Tong, Stephanie Tse, Phung Khanh Le, Kimberly Nguyen, Carrie B Brachmann, Douglas C Wallace & Taosheng Huang. (2008) The Molecular Mechanisms of OPA1-Mediated Optic Atrophy in Drosophila Model and Prospects for Antioxidant Treatment. PLoS Genetics 4:1, pages e6.
Crossref
Valerio Carelli, Chiara Morgia, Luisa Iommarini, Rosanna Carroccia, Marina Mattiazzi, Simonetta Sangiorgi, Sabrina Farne’, Alessandra Maresca, Beatrice Foscarini, Lucia Lanzi, Marcello Amadori, Marzio Bellan & Maria Lucia Valentino. (2007) Mitochondrial Optic Neuropathies: How Two Genomes may Kill the Same Cell Type?. Bioscience Reports 27:1-3, pages 173-184.
Crossref
Amy C. Cohn, Carmel Toomes, Catherine Potter, Katherine V. Towns, Alex W. Hewitt, Chris F. Inglehearn, Jamie E. Craig & David A. Mackey. (2007) Autosomal Dominant Optic Atrophy: Penetrance and Expressivity in Patients With OPA1 Mutations. American Journal of Ophthalmology 143:4, pages 656-662.e1.
Crossref
C. Hamel & G. Lenaers. (2007) Neuropathies optiques héréditaires. EMC - Ophtalmologie 4:3, pages 1-16.
Crossref
Jane W. Chan. 2007. Optic Nerve Disorders. Optic Nerve Disorders 171 200 .
Patrizia Amati‐Bonneau, Agnès Guichet, Aurélien Olichon, Arnaud Chevrollier, Frédérique Viala, Stéphanie Miot, Carmen Ayuso, Sylvie Odent, Catherine Arrouet, Christophe Verny, Marie‐Noelle Calmels, Gilles Simard, Pascale Belenguer, Jing Wang, Jean‐Luc Puel, Christian Hamel, Yves Malthièry, Dominique Bonneau, Guy Lenaers & Pascal Reynier. (2005) OPA1 R445H mutation in optic atrophy associated with sensorineural deafness. Annals of Neurology 58:6, pages 958-963.
Crossref
Chunmei Li, Gregory Kosmorsky, Kang Zhang, Bradley J. Katz, Jian Ge & Elias I. Traboulsi. (2005) Optic atrophy and sensorineural hearing loss in a family caused by an R445HOPA1 mutation. American Journal of Medical Genetics Part A 138A:3, pages 208-211.
Crossref
Anu Puomila, Kirsi Huoponen, Maija Mäntyjärvi, Petra Hämäläinen, Reetta Paananen, Eeva-Marja Sankila, Marja-Liisa Savontaus, Mirja Somer & Eeva Nikoskelainen. (2005) Dominant optic atrophy: correlation between clinical and molecular genetic studies. Acta Ophthalmologica Scandinavica 83:3, pages 337-346.
Crossref
Valerio Carelli, Fred N. Ross-Cisneros & Alfredo A. Sadun. (2004) Mitochondrial dysfunction as a cause of optic neuropathies. Progress in Retinal and Eye Research 23:1, pages 53-89.
Crossref
Patrizia Amati-Bonneau, Sylvie Odent, Christelle Derrien, Laurent Pasquier, Yves Malthi?ry, Pascal Reynier & Dominique Bonneau. (2003) The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 gene. American Journal of Ophthalmology 136:6, pages 1170-1171.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.