Zobrazeno 1 - 10
of 282
pro vyhledávání: '"Jl Dufier"'
Publikováno v:
Acta Ophthalmologica. 91
Purpose Many students understate their visual discomfort, although it may have an educational impact. We studied the prevalence of visual disorders among students without self-reported complaints. Methods Four hundred students between 15 and 22 years
Publikováno v:
Acta Ophthalmologica. 90
Purpose There is still no therapy for patients with Leber hereditary optic neuropathy (LHON). Recent studies have confirmed the effectiveness of Idebenone for the treatment of specific groups of LHON patients. However, it is still unclear if this tre
Autor:
Jl Dufier, C. Gaertner, Zoï Kapoula, Ma Espinasse-Berrod, Christophe Orssaud, Olivier Roche, C. Creux
Publikováno v:
Acta Ophthalmologica. 90
Purpose In healthy subjects, the postural stability in orthostatic position is better when fixating at near than at far distance; increased convergence angle contributes to such effect. Children with strabismus present a deficit in vergence movements
Autor:
K Gocho Nakashima, Jl Dufier, Olivier Roche, Nathalie Massamba, V. Parier, Jf Le Gargasson, B. Lamory, Nicolas Chateau, G. Soubrane
Publikováno v:
Acta Ophthalmologica. 86
Purpose The objective of this study was to develop an adaptive optics (AO) retinal imaging system and conduct in vivo pilot tests in a group of healthy eyes and in several pathological eyes. The experiments aimed at determining the device ability to
Publikováno v:
Europe PubMed Central
Pediatric retinal detachments differ from adult retinal detachments in their etiologies, prognosis and treatment. The aims of this study were the analysis and long-term follow-up of a group of pediatric retinal detachment patients.All the cases of ju
Autor:
Amiel J, Gagey V, Rabier D, Dorche C, Jean-Paul BONNEFONT, Jl, Dufier, Jm, Saudubray, Rey J, Munnich A
Publikováno v:
Europe PubMed Central
An enzyme deficiency can be demonstrated in 15 to 20% of cases of Leigh syndrome. A case of isolated sulphite oxidase deficiency is reported in a girl presenting with Leigh syndrome.An 8 month-old girl was admitted suffering from hypotonia and slow i
Publikováno v:
ResearcherID
Europe PubMed Central
Europe PubMed Central
The presence or absence of a recently observed mitochondrial DNA (mtDNA) mutation associated with Leber hereditary optic neuroretinopathy (LHON) was tested in 19 Finnish families with cases of LHON. Leukocyte and muscle DNA from individuals with opti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f2b5eaff2cb6fbad5e2fc3d117796bcc
https://europepmc.org/articles/PMC1682960/
https://europepmc.org/articles/PMC1682960/
Autor:
JL Dufier
Publikováno v:
Journal de Pédiatrie et de Puériculture. 8:124
Publikováno v:
Europe PubMed Central
Publikováno v:
Europe PubMed Central
A 19 year old male affected with Fabry's disease suffered from severe nervous manifestations. Despite very peculiar pains of the extremities, the diagnosis has been missed for a long time and was painted out at this age because of sharp reconstitutio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1e2257de794dded4c9186ea9b1e8fcad
http://europepmc.org/abstract/med/412484
http://europepmc.org/abstract/med/412484