Kolexia
Smirnov Vasily
Ophtalmologie
Hôpital Roger Salengro
Lille, France
70 Activités
0 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Rétinite pigmentaire Dystrophies rétiniennes Dystrophies des cônes et des batonnets Myopie Maladies héréditaires de l'oeil Dégénérescence maculaire Rétinopathies Rétinite Dystrophie des cônes

Industries

Merck-Serono
2 collaboration(s)
Dernière en 2021
OPUSLINE
2 collaboration(s)
Dernière en 2020
Alexion
2 collaboration(s)
Dernière en 2021
Novartis
1 collaboration(s)
Dernière en 2021

Dernières activités

Retinal arteriovenous malformation in Wyburn-Mason syndrome.
Journal francais d'ophtalmologie   19 février 2024
Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy.
Genetics in medicine : official journal of the American College of Medical Genetics   28 janvier 2024
Macular dystrophy in Kabuki syndrome due to de novo KMT2D variants: refining the phenotype with multimodal imaging and follow-up over 10 years: insight into pathophysiology.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie   11 janvier 2024
Stellate macular schisis.
Journal francais d'ophtalmologie   23 août 2023
PACS1-related syndrome: three cases with colobomas further delineating the phenotype
Abstracts from the 55th European Society of Human Genetics (ESHG) Conference   01 mai 2023
Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor beta.
Genetics in medicine : official journal of the American College of Medical Genetics   20 avril 2023
Mutational Spectrum, Ocular and Olfactory Phenotypes of -Related RP-Olfactory Dysfunction Syndrome in a Multiethnic Cohort.
Genes   30 mars 2023
Shedding light on myopia by studying complete congenital stationary night blindness.
Progress in retinal and eye research   19 janvier 2023
Association of Missense Variants in VSX2 With a Peculiar Form of Congenital Stationary Night Blindness Affecting All Bipolar Cells.
JAMA ophthalmology   19 décembre 2022
Retrospective Natural History Study of -Related Cone- and Cone-Rod Dystrophies While Expanding the Mutation Spectrum of the Disease.
International journal of molecular sciences   28 juin 2022