Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Roxane Machavoine"'
Autor:
Roxane Machavoine, Sylvie Helfre, Valérie Bernier, Stéphanie Bolle, Julie Leseur, Nadège Corradini, Angélique Rome, Anne-Sophie Defachelles, Sophie Deneuve, Sophie Bernard, Pierre Fayoux, Richard Nicollas, Michel Mondain, Romain Luscan, Françoise Denoyelle, François Simon, Natacha Kadlub, Fréderic Kolb, Jean-François Honart, Daniel Orbach, Véronique Minard-Colin, Antoine Moya-Plana, Vincent Couloigner
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2022)
IntroductionThe head and neck (HN) are the most frequent sites of pediatric rhabdomyosarcoma (RMS). Alveolar RMS (ARMS) represents ~20% of all RMS cases and frequently spread to lymph nodes (LNs). The aim was to report locoregional control, event-fre
Externí odkaz:
https://doaj.org/article/df053ecd4ffc4bf080994852a21417ff
Autor:
Alexandre Reymond, Paolo Gasparini, Jacqueline Chrast, Hannie Kremer, Sissy Bassani, Giorgia Girotto, Jiddeke M. van de Kamp, Massimiliano Cocca, Nicolas Guex, Benjamin Delprat, Mireille Rossel, Francesca Amati, Flavio Faletra, Heiko Locher, Yoan Arribat, Sylvain Pradervand, Alban Ziegler, Jeroen Smits, Sandrine Marlin, Norine Voisin, Giuliana Giannuzzi, Tangui Maurice, Anna Morgan, Roxane Machavoine, Edward S A van Beelen, Nicolas Chatron
Publikováno v:
Bassani, S, van Beelen, E, Rossel, M, Voisin, N, Morgan, A, Arribat, Y, Chatron, N, Chrast, J, Cocca, M, Delprat, B, Faletra, F, Giannuzzi, G, Guex, N, Machavoine, R, Pradervand, S, Smits, J J, van de Kamp, J M, Ziegler, A, Amati, F, Marlin, S, Kremer, H, Locher, H, Maurice, T, Gasparini, P, Girotto, G & Reymond, A 2021, ' Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss ', Human Molecular Genetics, vol. 30, no. 19, pp. 1785-1796 . https://doi.org/10.1093/hmg/ddab145
Human Molecular Genetics, 30(19), 1785-1796. OXFORD UNIV PRESS
Human Molecular Genetics, 30(19), 1785-1796. Oxford University Press
Human Molecular Genetics, 30, 19, pp. 1785-1796
Human Molecular Genetics, 30, 1785-1796
Human Molecular Genetics, 30(19), 1785-1796. OXFORD UNIV PRESS
Human Molecular Genetics, 30(19), 1785-1796. Oxford University Press
Human Molecular Genetics, 30, 19, pp. 1785-1796
Human Molecular Genetics, 30, 1785-1796
Non-Syndromic Hereditary Hearing Loss (NSHHL) is a genetically heterogeneous sensory disorder with about 120 genes already associated. Through exome sequencing (ES) and data aggregation, we identified a family with six affected individuals and one un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f04c37bdd5fbeef500c5817cdbe20bc
https://doi.org/10.1093/hmg/ddab145
https://doi.org/10.1093/hmg/ddab145
Autor:
Roxane Machavoine, Michel Brachet, Claire-Sophie Bich, Alexandre Duhoux, Arnaud Baus, E. Bey, Anne Lakhel, P Duhamel
Publikováno v:
Revue Francophone de Cicatrisation. 3:10-14
La brulure se definit par une destruction tissulaire secondaire a l’agression du revetement cutane, voire des structures sous-jacentes, consecutive a l’action d’agents thermiques, electriques, chimiques ou radiologiques. L’objectif de cet art
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8eed04244603c0f96cd1c6ae0cfe85bf
https://doi.org/10.1016/j.refrac.2019.06.001
https://doi.org/10.1016/j.refrac.2019.06.001