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Scholar Results 1 - 2 of 2 citing Patel: Importance of molecular testing in dominant optic atrophy. (0.07 sec) 

Novel mutations in the OPA1 gene and associated clinical features in Japanese patients with …


M Nakamura, J Lin, S Ueno, R Asaoka, T Hirai … - Ophthalmology, 2006 - Elsevier
Autosomal dominant optic atrophy (ADOA) is characterized by symmetrical
bilateral optic atrophy associated with reduced corrected visual acuity (VA),
central or centrocecal scotoma, and color vision disturbances. The disease ...
Cited by 7 - Related articles - All 9 versions

Reduction of inner retinal thickness in patients with autosomal dominant optic atrophy …

- iovs.org
Y Ito, M Nakamura, T Yamakoshi, J Lin, H … - Investigative Ophthalmology & Visual Science, 2007 - ARVO
METHODS. Cross-sectional images of the macular area of the retina were obtained
by optical coherence tomography (OCT) in patients with ADOA who had a
heterozygous mutation in the OPA1 gene. There were 15 eyes of eight ...
Cited by 2 - Related articles - BL Direct - All 2 versions


 


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