F.X. Borruat

Discipline

Psychologie (7) Gestion et management (1)

Type de document

Articles (13) Recensions (1)

Co-auteur

Date

Source

Mot-clé

Patients (7) Patients (7) Examination (7) Cases (6) Retinal (Visual pigment) (6) Eye (6) Evaluation (6) Cases (6) Visual acuity (5) Vision (5) Symptoms (5) Older people (5) Optical coherence tomography (5) mise sous écran protecteur (4) mutation (4) perte (4) littérature (4) Testing (4) Women (4) Testing (4) Human beings (4) Literature (4) Families (4) Electroretinography (4) Tax assessment (4) Mutation (4) femme (3) temps (durée) (3) champ (3) famille (3)

Documents écrit par F.X. Borruat (13) | parle de F.X. Borruat (0)

Homonymous visual field defects in patients with multiple sclerosis: results of computerised perimetry and optical coherence tomography.
L. Schmutz et al. (7 sept. 2020)
Cross-sectional study assessing the addition of contrast sensitivity to visual acuity when testing for fitness to drive.
L. Spreng et al. (26 janv. 2018)
Inner Retinal Dysfunction in the Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.
F.X. Borruat et al. (2017)
Spectrum of digoxin-induced ocular toxicity: a case report and literature review.
D. Renard et al. (2015)
Paraneoplastic Vitelliform Retinopathy Secondary to Metastatic Melanoma.
P.G. Meier et al. (2015)
Visual signs and symptoms in patients with the visual variant of Alzheimer disease.
P.F. Kaeser et al. (2015)
Macular dystrophy associated with the mitochondrial DNA A3243G mutation: pericentral pigment deposits or atrophy? Report of two cases and review of the literature.
A. Daruich et al. (2014)
Posterior cortical atrophy: review of the recent literature.
F.X. Borruat (2013)
Acquired oscillopsia: potential complication after multifocal IOL implantation
E. Gkaragkani et al. (2013)
Double Concentric Autofluorescence Ring in NR2E3-p.G56R-linked Autosomal Dominant Retinitis Pigmentosa.
P. Escher et al. (2012)
The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone, and macular dystrophy.
M. Michaelides et al. (2010)
Unsatisfactory outcomes in myasthenia gravis: influence by care providers.
M. Dunand et al. (2010)
Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 gene.
L. El Matri et al.