Kolexia
Mouallem Alexandra
Ophtalmologie
Centre Ophtalmologique Jean Jaures
Toulouse, France
37 Activités
313 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Dégénérescence maculaire Décollement de la rétine Dégénérescence maculaire humide Rétinopathies Dégénérescence de la rétine Cécité Néovascularisation choroïdienne Maladies héréditaires de l'oeil Myopie

Industries

Bayer
7 collaboration(s)
Dernière en 2023
Thea
3 collaboration(s)
Dernière en 2022
Sanofi
2 collaboration(s)
Dernière en 2020
DORC France
2 collaboration(s)
Dernière en 2023

Dernières activités

Optical coherence tomography angiography analysis of changes in the retina and the choroid after hemodialysis for end stage kidney disease.
International ophthalmology   17 août 2023
ARI2: A Phase III b, Multicenter Study of the Efficacy and Safety of Aflibercept Switch in Patients With Exudative AMD With Detachment of the Retinal Pigment Epithelium and Previously Treated With Ranibizumab Intravitreal Injection. (ARI2)
Essai Clinique (Bayer)   05 décembre 2022
OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY IMAGING OF CHOROIDAL NEOVASCULARIZATION SECONDARY TO CHOROIDAL RUPTURE TREATED BY INTRAVITREAL RANIBIZUMAB.
Retinal cases & brief reports   22 mars 2022
Diabète avec surdité de transmission maternelle (MIDD) : à propos d'un cas
Edimark   31 décembre 2021
The Spectrum of Central Choriocapillaris Abnormalities on Swept-Source Optical Coherence Tomography Angiography in the Fellow Eye of Unilateral Exudative Age-Related Macular Degeneration Patients: From Flow Deficits to Subclinical Non-Exudative Neovascularization.
Journal of clinical medicine   16 juin 2021
GENETICS OF LARGE PIGMENT EPITHELIAL DETACHMENTS IN NEOVASCULAR AGE-RELATED MACULAR DEGENERATION.
Retina (Philadelphia, Pa.)   04 mai 2021
Loss of function of RIMS2, a synaptic membrane exocytosis gene, causes a new phenotype characterized by congenital cone-rod synaptic disease associated with neurodevelopmental and pancreatic involvement
Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference   01 décembre 2020
of function of RIMS2 , a synaptic membrane exocytosis gene, causes a new phenotype characterized by congenital cone-rod synaptic disease associated with neurodevelopmental and pancreatic involvement
Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference   01 décembre 2020
Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement.
American journal of human genetics   03 octobre 2020
A case of undiagnosed X-linked retinoschisis presenting as unilateral macular demarcation line.
European journal of ophthalmology   22 juillet 2020