Search Page
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
Search Results
3 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Lattice corneal dystrophy type I without typical lattice lines: role of mutational analysis.
Am J Ophthalmol. 2004 Mar;137(3):586-8. doi: 10.1016/j.ajo.2003.09.003.
Am J Ophthalmol. 2004.
PMID: 15013897
Novel mutation in FZD4 gene in a Japanese pedigree with familial exudative vitreoretinopathy.
Yoshida S, Arita R, Yoshida A, Tada H, Emori A, Noda Y, Nakao S, Fujisawa K, Ishibashi T.
Yoshida S, et al. Among authors: emori a.
Am J Ophthalmol. 2004 Oct;138(4):670-1. doi: 10.1016/j.ajo.2004.05.001.
Am J Ophthalmol. 2004.
PMID: 15488808
Item in Clipboard
Cognitive dysfunction in systemic lupus erythematosus.
Emori A, Matsushima E, Aihara O, Ohta K, Koike R, Miyasaka N, Kato M.
Emori A, et al.
Psychiatry Clin Neurosci. 2005 Oct;59(5):584-9. doi: 10.1111/j.1440-1819.2005.01418.x.
Psychiatry Clin Neurosci. 2005.
PMID: 16194262
Free article.
Clinical Trial.
Item in Clipboard
Cite
Cite