Selective wavelength pupillometry in Leber hereditary optic neuropathy.

Details

Request a copyRequest a copy
Serval ID
serval:BIB_1C8BAA9D740E
Type
Article: article from journal or magazin.
Publication sub-type
Case report (case report): feedback on an observation with a short commentary.
Collection
Publications
Institution
UNIL/CHUV
Title
Selective wavelength pupillometry in Leber hereditary optic neuropathy.
Journal
Clinical and Experimental Ophthalmology
Author(s)
Kawasaki A., Herbst K., Sander B., Milea D.
ISSN
1442-9071[electronic], 1442-6404[linking]
Publication state
Published
Issued date
2010
Peer-reviewed
Oui
Volume
38
Number
3
Pages
322-324
Language
english
Notes
Publication types: Case Reports ; Letter
Publication Status: ppublish
Keywords
Adult, Color Vision, Female, Humans, Light, Mutation, Optic Atrophy, Hereditary, Leber/genetics, Optic Atrophy, Hereditary, Leber/physiopathology, Pupil/physiology, Retinal Ganglion Cells/pathology, Retinal Ganglion Cells/physiology, Rod Opsins/physiology, Vision Disorders/etiology, Vision, Monocular
OAI-PMH
oai:serval.unil.ch:BIB_1C8BAA9D740E
Pubmed
20447133
Web of science
000276949000019
Create date
17/12/2010 9:09
Last modification date
20/08/2019 12:53
Usage data