Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ninon Ternoy"'
Autor:
Rémi Karadayi, Charlotte Pallot, Stéphanie Cabaret, Julie Mazzocco, Pierre-Henry Gabrielle, Denis S. Semama, Corinne Chantegret, Ninon Ternoy, Delphine Martin, Aurélie Donier, Stéphane Gregoire, Catherine P. Creuzot-Garcher, Alain M. Bron, Lionel Bretillon, Olivier Berdeaux, Niyazi Acar
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
N-3 polyunsaturated fatty acids (PUFAs) may prevent retinal vascular abnormalities observed in oxygen-induced retinopathy, a model of retinopathy of prematurity (ROP). In the OmegaROP prospective cohort study, we showed that preterm infants who will
Externí odkaz:
https://doaj.org/article/bcf0f07de2974354a418efbccbf0a72a
Autor:
Mylène Tharreau, Aurore Garde, Sandrine Marlin, Godelieve Morel, Sylvain Ernest, Sophie Nambot, Yannis Duffourd, Ninon Ternoy, Christian Duvillard, Siddharth Banka, Christophe Philippe, Christel Thauvin‐Robinet, Frederic Tran Mau‐Them, Laurence Faivre
Publikováno v:
Tharreau, M, Garde, A, Marlin, S, Morel, G, Ernest, S, Nambot, S, Duffourd, Y, Ternoy, N, Duvillard, C, Banka, S, Philippe, C, Thauvin-Robinet, C, Mau-Them, F T & Faivre, L 2022, ' Refining the clinical phenotype associated with missense variants in exons 38 and 39 of KMT2D ', American Journal of Medical Genetics. Part A . https://doi.org/10.1002/ajmg.a.62642
Loss-of-function variants in KMT2D are responsible for Kabuki syndrome type 1 (KS1). In the last 5 years, missense variants in exon 38 or 39 in KMT2D have been found in patients exhibiting a new phenotype with multiple malformations and absence of in
Publikováno v:
Revue Francophone des Laboratoires. 2018:24-29
Resume Le pediatre neonatologiste prend en charge des nouveau-nes de faible poids de naissance, particulierement sensibles aux infections qui peuvent mettre en jeu leur pronostic vital. Il doit donc disposer d’outils diagnostiques lui permettant d
Autor:
Stéphane Grégoire, Niyazi Acar, Denis S. Semama, Julie Mazzocco, Ninon Ternoy, Charlotte Pallot, Cyril Meillon, Lionel Bretillon, Catherine Creuzot-Garcher, Corinne Chantegret, Alain M. Bron, Delphine Martin, Aurélie Donier
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2019, 9 (1), pp.7930. ⟨10.1038/s41598-019-44476-w⟩
Scientific Reports 1 (9), 7930. (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Scientific Reports, Nature Publishing Group, 2019, 9 (1), pp.7930. ⟨10.1038/s41598-019-44476-w⟩
Scientific Reports 1 (9), 7930. (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Extremely preterm infants are at high risk for retinopathy of prematurity (ROP), a potentially blinding disease characterized by abnormalities in retinal vascularization. Whereas animal studies revealed that n-3 polyunsaturated fatty acids (PUFAs) ma
Autor:
Agnès Soudry Faure, Catherine Creuzot-Garcher, Ninon Ternoy, Claude Speeg Schatz, Niyazi Acar, Camille Charvy, Charlotte Pallot, Alain M. Bron, Claire Langlet Muteau
Publikováno v:
Ophthalmic Research
Ophthalmic Research, Karger, 2018, 59 (4), pp.228-234. ⟨10.1159/000477622⟩
Ophthalmic Research, Karger, 2018, 59 (4), pp.228-234. ⟨10.1159/000477622⟩
Purpose: To determine the factors influencing the time from preterm birth and retinopathy of prematurity (ROP) detection to optimize the timing of the initial screening. Methods: This multicenter retrospective study enrolled preterm infants born befo