Results 221 to 230 of about 1,459,190 (233)

Electrophysiological and Histologic Assessment of Retinal Ganglion Cell Fate in a Mouse Model for OPA1-Associated Autosomal Dominant Optic Atrophy

Investigative Ophthalmology and Visual Science, 2010
Bernd Wissinger, Marcel V. Alavi, Sven Schnichels   +2 more
exaly  

[Hereditary optic atrophies. Study of a family with dominant autosomal optic atrophy].

Revista clinica espanola, 1982
M, Sebastián de Erice, J, Romero López, J, Navarro Esteban, F, Jiménez, L, Soto Faure   +4 more
openaire   +1 more source

Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment†

American Journal of Medical Genetics, Part A, 2011
Nanna Dahl Rendtorff, Arti Pandya, Lars H. Hansen   +2 more
exaly  

A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy

Journal of Neurology, 2005
Gian Nicola Gallus, Alessandra Rufa, Antonio Federico   +2 more
exaly  

Optic Atrophy, Autosomal Dominant, Kjer Type

2012
openaire   +1 more source

Retinal vessel diameters decrease with macular ganglion cell layer thickness in autosomal dominant optic atrophy and in healthy subjects

Acta Ophthalmologica, 2014
Karen Grønskov, Michael Larsen, Cecilia Rönnbäck   +2 more
exaly  

Reduction of Oscillatory Potentials and Photopic Negative Response in Patients with Autosomal Dominant Optic Atrophy with OPA1 Mutations

Investigative Ophthalmology and Visual Science, 2007
Makoto Nakamura, Hiroko Terasaki
exaly  

[Benign autosomal dominant hereditary optic atrophy].

Bulletin des societes d'ophtalmologie de France, 1986
P, Verin, P, Comte
openaire   +1 more source

Electrophysiological ON and OFF Responses in Autosomal Dominant Optic Atrophy

Investigative Ophthalmology and Visual Science, 2015
Enyam Komla Amewuho Morny, Marcela Votruba   +1 more
exaly  

Optic Atrophy 3, Autosomal Dominant (OPA3)

openaire   +1 more source