Ophthalmic manifestations of inherited neurodegenerative disorders-Reference-Cited by-同舟云学术

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Ophthalmic manifestations of inherited neurodegenerative disorders

Published:2014-05-20 Issue:6 Volume:10 Page:349-362
ISSN:1759-4758
Container-title:Nature Reviews Neurology
language:en
Short-container-title:Nat Rev Neurol

Author:

Kersten Hannah M.,Roxburgh Richard H.,Danesh-Meyer Helen V.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical)

Link

http://www.nature.com/articles/nrneurol.2014.79.pdf

Reference211 articles.

1. Chung, K. W. et al. Early onset severe and late-onset mild Charcot–Marie–Tooth disease with mitofusin 2 (MFN2) mutations. Brain 129, 2103–2118 (2006).

2. Fortuna, F. et al. Visual system involvement in patients with Friedreich's ataxia. Brain 132, 116–123 (2009).

3. Klebe, S. et al. Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy. Brain 135, 2980–2993 (2012).

4. Pula, J. H., Gomez, C. M. & Kattah, J. C. Ophthalmologic features of the common spinocerebellar ataxias. Curr. Opin. Ophthalmol. 21, 447–453 (2010).

5. Grainger, B. T., Papchenko, T. L. & Danesh-Meyer, H. V. Optic nerve atrophy in adrenoleukodystrophy detectable by optic coherence tomography. J. Clin. Neurosci. 17, 122–124 (2010).

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