Results 91 to 100 of about 206 (103)

Optic Atrophy as the Presenting Sign in Hallervorden-Spatz Syndrome

Neuropediatrics, 1994
I Casteels, P Casaer, P Demaerel
exaly  

Optic atrophy in Wolfram (DIDMOAD) syndrome

Eye, 1997
Timothy G Barrett, A R Fielder, P A Good
exaly  

Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy (PEHO) syndrome in a Swiss child

European Journal of Paediatric Neurology, 2004
Eugen Boltshauser
exaly  

The syndrome of diabetes insipidus, diabetes mellitus, optic atrophy, deafness, and other abnormalities (DIDMOAD-Syndrome)

Klinische Wochenschrift, 1982
H W Rüdiger, J Kühnau, H Bartelheimer   +2 more
exaly  

Dutch Patients with Progressive Encephalopathy with Edema, Hypsarrhythmia, and Optic Atrophy (PEHO) Syndrome

Neuropediatrics, 2002
S Vanhatalo, P G Barth
exaly  

Optic atrophy as the first symptom in Hallervorden-Spatz syndrome

Child's Nervous System, 2014
Pier Antonio Battistella, Edoardo Midena, Agnese Suppiej   +2 more
exaly  

Diabetes mellitus, diabetes insipidus, optic atrophy, and deafness: A case of Wolfram (DIDMOAD) syndrome

Journal of Current Ophthalmology, 2015
Nasrollah Maleki, Bahman Bashardoust, Anahita Zakeri   +2 more
exaly  

Clinical variability in hereditary optic neuropathies: Two novel mutations in two patients with dominant optic atrophy and Wolfram syndrome

Saudi Journal of Ophthalmology, 2015
Alberto Gálvez-Ruiz
exaly  

Progressive Encephalopathy with Edema, Hypsarrhythmia, and Optic Atrophy (PEHO Syndrome) in Two Japanese Siblings

Neuropediatrics, 1995
exaly  

WFS1 in Optic Neuropathies: Mutation Findings in Nonsyndromic Optic Atrophy and Assessment of Clinical Severity

Ophthalmology, 2016
Isabelle Meunier, Vincent Daien, François Halloy   +2 more
exaly