Zobrazeno 1 - 10
of 1 426
pro vyhledávání: '"Claustres, A."'
Autor:
Bergougnoux, A., Billet, A., Ka, C., Heller, M., Degrugillier, F., Vuillaume, M.-L., Thoreau, V., Sasorith, S., Bareil, C., Thèze, C., Ferec, C., Gac, G. Le, Bienvenu, T., Bieth, E., Gaston, V., Lalau, G., Pagin, A., Malinge, M.-C., Dufernez, F., Lemonnier, L., Koenig, M., Fergelot, P., Claustres, M., Taulan-Cadars, M., Kitzis, A., Reboul, M.-P., Becq, F., Fanen, P., Mekki, C., Audrezet, M.-P., Girodon, E., Raynal, C.
Publikováno v:
In Journal of Cystic Fibrosis May 2023 22(3):515-524
Akademický článek
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Autor:
Gouin, Olivier, Barbieux, Claire, Leturcq, Florent, Bonnet des Claustres, Mathilde, Petrova, Evgeniya, Hovnanian, Alain
Publikováno v:
In Journal of Investigative Dermatology June 2020 140(6):1184-1194
Autor:
L. Gandois, A. M. Hoyt, S. Mounier, G. Le Roux, C. F. Harvey, A. Claustres, M. Nuriman, G. Anshari
Publikováno v:
Biogeosciences, Vol 17, Pp 1897-1909 (2020)
Worldwide, peatlands are important sources of dissolved organic matter (DOM) and trace metals (TMs) to surface waters, and these fluxes may increase with peatland degradation. In Southeast Asia, tropical peatlands are being rapidly deforested and dra
Externí odkaz:
https://doaj.org/article/428255592dce402fad9f85aa11004bde
Autor:
Bergougnoux, A., Délétang, K., Pommier, A., Varilh, J., Houriez, F., Altieri, J.P., Koenig, M., Férec, C., Claustres, M., Lalau, G., Bienvenu, T., Audrézet, M.P., Pagin, A., Girodon, E., Raynal, C., Taulan-Cadars, M.
Publikováno v:
In Journal of Cystic Fibrosis July 2019 18(4):468-475
Autor:
Girardet, Anne *, Ishmukhametova, Aliya, Viart, Victoria, Plaza, Stéphanie, Saguet, Florielle, Verriere, Garance, Hamamah, Samir, Coupier, Isabelle, Haquet, Emmanuelle, Anahory, Tal, Willems, Marjolaine, Claustres, Mireille
Publikováno v:
In Reproductive BioMedicine Online February 2018 36(2):154-163
Autor:
Chiara Passarelli, Rita Selvatici, Alberto Carrieri, Francesca Romana Di Raimo, Maria Sofia Falzarano, Fernanda Fortunato, Rachele Rossi, Volker Straub, Katie Bushby, Mojgan Reza, Irina Zharaieva, Adele D’Amico, Enrico Bertini, Luciano Merlini, Patrizia Sabatelli, Paola Borgiani, Giuseppe Novelli, Sonia Messina, Marika Pane, Eugenio Mercuri, Mireille Claustres, Sylvie Tuffery-Giraud, Annemieke Aartsma-Rus, Pietro Spitali, Peter A. C. T’Hoen, Hanns Lochmüller, Kristin Strandberg, Cristina Al-Khalili, Ekaterina Kotelnikova, Michael Lebowitz, Elena Schwartz, Francesco Muntoni, Chiara Scapoli, Alessandra Ferlini
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
BackgroundDuchenne muscular dystrophy (DMD) is a rare and severe X-linked muscular dystrophy in which the standard of care with variable outcome, also due to different drug response, is chronic off-label treatment with corticosteroids (CS). In order
Externí odkaz:
https://doaj.org/article/b81fc57f071f44379d499b268e34d2eb
Autor:
Fanny Pineau, Davide Caimmi, Milena Magalhães, Enora Fremy, Abdillah Mohamed, Laurent Mely, Sylvie Leroy, Marlène Murris, Mireille Claustres, Raphael Chiron, Albertina De Sario
Publikováno v:
PLoS ONE, Vol 15, Iss 4, p e0231285 (2020)
Cystic fibrosis (CF) is a rare genetic disease that affects the respiratory and digestive systems. Lung disease is variable among CF patients and associated with the development of comorbidities and chronic infections. The rate of lung function deter
Externí odkaz:
https://doaj.org/article/19c4c9e3fc364f8cb90d71fb62026498
Autor:
Victoria Viart, Aliya Ishmukhametova, Stéphanie Plaza, Garance Verrière, Florielle Saguet, Mireille Claustres, Anne Girardet
Publikováno v:
European Medical Journal Reproductive Health, Vol 4, Iss 1, Pp 83-87 (2018)
Background: Cystic fibrosis (CF) is one of the most common indications of preimplantation genetic diagnosis (PGD) for monogenic disorders worldwide. Aims: The aim of this article was to report a universal and powerful assay easily applicable to al
Externí odkaz:
https://doaj.org/article/6224f8184a474e58b10cdb02472b17b2
Autor:
Luke Mansard, David Baux, Christel Vaché, Catherine Blanchet, Isabelle Meunier, Marjolaine Willems, Valérie Faugère, Corinne Baudoin, Melody Moclyn, Julie Bianchi, Helene Dollfus, Brigitte Gilbert-Dussardier, Delphine Dupin-Deguine, Dominique Bonneau, Isabelle Drumare, Sylvie Odent, Xavier Zanlonghi, Mireille Claustres, Michel Koenig, Vasiliki Kalatzis, Anne-Françoise Roux
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 24, p 13294 (2021)
Usher syndrome is an autosomal recessive disorder characterized by congenital hearing loss combined with retinitis pigmentosa, and in some cases, vestibular areflexia. Three clinical subtypes are distinguished, and MYO7A and USH2A represent the two m
Externí odkaz:
https://doaj.org/article/60bf793686c64932a496b57b4a231434