Zobrazeno 1 - 10
of 102
pro vyhledávání: '"A. Chantegret"'
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:
Forner, O., Schiby, A., Ridley, A., Thiriez, G., Mugabo, I., Morel, V., Mulin, B., Filiatre, J.-C., Riethmuller, D., Levy, G., Semama, D., Martin, D., Chantegret, C., Bert, S., Godoy, F., Sagot, P., Rousseau, T., Burguet, A.
Publikováno v:
In Archives de pédiatrie August 2018 25(6):383-388
Autor:
Robert Olaso, Adeline Prost, Anne-Sophie Denommé-Pichon, Magali Gorce, Anne Boland, Mélanie Fradin, Magalie Barth, Mathilde Nizon, Antonio Vitobello, Dominique Bonneau, Bertrand Isidor, Christel Thauvin-Robinet, Frédéric Tran Mau-Them, Victor Couturier, Caroline Racine, Céline Besse, Marie Vincent, Bertrand Fin, Yline Capri, Alban Ziegler, Ange-Line Bruel, Yannis Duffourd, Christophe Philippe, P. Callier, Sébastien Moutton, Aurore Garde, Médéric Jeanne, Annick Toutain, Sophie Nambot, Delphine Bacq-Daian, Charlotte Poë, Emilie Tisserant, Aurélien Juven, Julien Van-Gils, Tiffany Busa, Laurent Pasquier, Sabine Sigaudy, Arthur Sorlin, Thibaud Jouan, Philippine Garret, Corinne Chantegret, Julian Delanne, Cyril Flamant, Alinoë Lavillaureix, Clement Prouteau, Paul Rollier, Laurence Faivre, Jean-François Deleuze
Publikováno v:
Eur J Hum Genet
Obtaining a rapid etiological diagnosis for infants with early-onset rare diseases remains a major challenge. These diseases often have a severe presentation and unknown prognosis, and the genetic causes are very heterogeneous. In a French hospital n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a96c47fea7bf31535b63687ed6bc425c
https://doi.org/10.1038/s41431-021-00998-4
https://doi.org/10.1038/s41431-021-00998-4
Akademický článek
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Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Boissier, K., Varlet, M.-N., Chauleur, C., Cochin, S., Clemenson, A., Varlet, F., Bellicard, E., Chantegret, C., Patural, H., Seffert, P., Chêne, G.
Publikováno v:
In Gynécologie Obstétrique & Fertilité 2009 37(2):115-124
Autor:
Béjot, Y., Chantegret, C., Osseby, G.-V., Chouchane, M., Huet, F., Moreau, T., Gouyon, J.-B., Giroud, M.
Publikováno v:
In Revue Neurologique 2009 165(11):889-900
Autor:
E. Herquelot, M. Robaszkiewicz, N. Saidani, M. Chantegret, D. Bernardini, E. Boutin, S. Koch, F. Tesiorowski, G. Plessia, O. Gronier, L. Lamarsalle, S. Chaussade
Publikováno v:
Revue d'Épidémiologie et de Santé Publique. 70:S127
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44284361a645d9f5eb452cc29887986d
https://doi.org/10.1016/j.respe.2022.03.072
https://doi.org/10.1016/j.respe.2022.03.072
Autor:
D. Riethmuller, G. Levy, A. Burguet, S. Bert, D. Martin, B. Mulin, P. Sagot, D.S. Semama, Gérard Thiriez, O. Forner, C. Chantegret, A. Ridley, A. Schiby, V. Morel, I. Mugabo, T. Rousseau, J.-C. Filiatre, F. Godoy
Publikováno v:
Archives de Pédiatrie. 25:383-388
OBJECTIVES Mortality rates of very preterm infants may vary considerably between healthcare facilities depending on the neonates' place of inclusion in the cohort study. The objective of this study was to compare the mortality rates of live-born extr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0429d7c332bde6830eaedde6542268e6
https://doi.org/10.1016/j.arcped.2018.06.006
https://doi.org/10.1016/j.arcped.2018.06.006
Autor:
Joshi Stephen, Alexander G. Bassuk, Hatem El-Shanti, Yasser Al-Sarraj, Christel Thauvin-Robinet, May Christine V. Malicdan, Judith St-Onge, William P. Bone, James C. Mullikin, Ariane Soldatos, Yannis Dufford, Jean Baptiste Rivière, Tawfeg Ben-Omran, Alice Masurel-Paulet, Julien Thevenon, Jamil Al-Alami, Allison Cox, Hala Boulos, Marios Kambouris, William A. Gahl, Corrine Chantegret, Nisc Comparative Sequencing Program, Laurence Faivre
Publikováno v:
Annals of Clinical and Translational Neurology. 4:26-35
Objectives Two consanguineous families, one of Sudanese ethnicity presenting progressive neuromuscular disease, severe cognitive impairment, muscle weakness, upper motor neuron lesion, anhydrosis, facial dysmorphism, and recurrent seizures and the ot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c775f83f029560249a3a4a11b843d8d4
https://doi.org/10.1002/acn3.372
https://doi.org/10.1002/acn3.372