Product
Help
Pricing
About
Jobs
Log in
Get started
Author
Add to collection
Clément Paya
Observed names:
C Paya,
C. Paya,
Clement Paya,
PAYA, Clément
Observed institutions:
Universidade Federal do Rio de Janeiro,
Université de Bordeaux,
Tel Aviv Sourasky Medical Center,
Centre Hospitalier Universitaire de Bordeaux,
Hôpital Pellegrin
OpenAlex ID:
A5110091069
Mild form of oculocutaneous albinism type 1: phenotypic analysis of compound heterozygous patients with the R402Q variant of the TYR gene
2018
·
Solene Monfermé
, Eulalie Lasseaux
, et al.
·
British Journal of Ophthalmology
·
45
Potential of FTIR spectroscopy for analysis of tears for diagnosis purposes
2014
·
Adrian Travo
, Clément Paya
, et al.
·
Analytical and Bioanalytical Chemistry
·
45
Lessons of a day hospital: Comprehensive assessment of patients with albinism in a European setting
2017
·
Aurélie Marti
, Eulalie Lasseaux
, et al.
·
Pigment Cell & Melanoma Research
·
37
Evolution Profiles of Different Corneal Parameters in Progressive Keratoconus
2016
·
Joy Tellouck
, David Touboul
, et al.
·
Cornea
·
25
Wavefront Analysis After Wavefront-Guided Myopic LASIK Using a New Generation Aberrometer
2014
·
David Smadja
, Tania De Castro
, et al.
·
Journal of Refractive Surgery
·
18
Spontaneous rupture of chorioretinal coloboma in an 8-year-old child is treated by temporal fascia graft
2016
·
Hélène Chan
, Marie-Noëlle Delyfer
, et al.
·
Journal of American Association for Pediatric Ophthalmology and Strabismus
·
6
Retinopathy of prematurity associated with oculocutaneous albinism: Laser treatment is not an option
2019
·
Camille Costet
, Laurent Renesme
, et al.
·
Journal Français d Ophtalmologie
·
1
Retinopathy of Prematurity Evolution After Laser Treatment
2015
·
Valentine Coste
, Clément Paya
, et al.
·
JAMA Ophthalmology
·
1
Amblyogramme numérique : retour d’expérience après un an d’utilisation en cabinet d’ophtalmo-pédiatrie
2026
·
Fanny Lecomte
, Dominique Thouvenin
, et al.
·
Revue Francophone d Orthoptie
A Rare Form of Microcephalic Primordial Dwarfism due to NSMCE2 Deficiency (Seckel Syndrome Type 10): A Report of Macular Involvement
2026
·
Cristina Peduto
, Céline Huber
, et al.
·
American Journal of Medical Genetics Part A
PDF
Iconography : Astrocytome rétinien dans le cadre d’une sclérose tubéreuse de Bourneville : apport de l’OCT spectral domain
2014
·
V Coste
, C Paya
, et al.
Glaukom flecken
2010
·
C. Paya
, C. Schweitzer
, et al.
·
Journal Français d Ophtalmologie
Show more works
View as search
Works count:
13
Citation count:
178
H-index:
6
I10-index:
5
Year
Topic
Type