Outcomes of 38 patients with PFIC3: Impact of genotype and of response to ursodeoxycholic acid therapy

Autor: Gonzales, Emmanuel, Gardin, Antoine, Almes, Marion, Darmellah-Remil, Amaria, Seguin, Hanh, Mussini, Charlotte, Franchi-Abella, Stéphanie, Duché, Mathieu, Ackermann, Oanez, Thébaut, Alice, Habes, Dalila, Hermeziu, Bogdan, Lapalus, Martine, Falguières, Thomas, Combal, Jean-Philippe, Benichou, Bernard, Valero, Sonia, Davit-Spraul, Anne, Jacquemin, Emmanuel

Publikováno v: In JHEP Reports October 2023 5(10)

Long-term outcome of combined radiologic and surgical strategy for the management of biliary complications after pediatric liver transplantation.

Autor: Calinescu, Ana M., Monluc, Sébastien, Franchi-Abella, Stephanie, Habes, Dalila, Weber, Gabrielle, Almes, Marion F., Waguet, Jerome, Jacquemin, Emmanuel, Fouquet, Virginie, Miatello, Jordi, Hery, Geraldine, Baujard, Catherine, Gonzales, Emmanuel, Branchereau, Sophie, Guérin, Florent

Publikováno v: BMC Research Notes; 3/20/2024, Vol. 17 Issue 1, p1-7, 7p

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Corrigendum to 'ATP7B variant spectrum in a French pediatric Wilson disease cohort' [Eur. J. Med. Genet. 64(10) (2021) 104305] (European Journal of Medical Genetics (2021) 64(10), (S1769721221001713), (10.1016/j.ejmg.2021.104305))

Autor: Couchonnal, Eduardo, Bouchard, Sophie, Sandahl, Thomas Damgaard, Pagan, Cecile, Lion-François, Laurence, Guillaud, Olivier, Habes, Dalila, Debray, Dominique, Lamireau, Thierry, Broué, Pierre, Fabre, Alexandre, Vanlemmens, Claire, Sobesky, Rodolphe, Gottrand, Frederic, Bridoux-Henno, Laure, Belmalih, Abdelouahed, Poujois, Aurelia, Brunet, Anne Sophie, Lachaux, Alain, Bost, Muriel

Publikováno v: Couchonnal, E, Bouchard, S, Sandahl, T D, Pagan, C, Lion-François, L, Guillaud, O, Habes, D, Debray, D, Lamireau, T, Broué, P, Fabre, A, Vanlemmens, C, Sobesky, R, Gottrand, F, Bridoux-Henno, L, Belmalih, A, Poujois, A, Brunet, A S, Lachaux, A & Bost, M 2021, ' Corrigendum to “ATP7B variant spectrum in a French pediatric Wilson disease cohort” [Eur. J. Med. Genet. 64(10) (2021) 104305] (European Journal of Medical Genetics (2021) 64(10), (S1769721221001713), (10.1016/j.ejmg.2021.104305)) ', European Journal of Medical Genetics, vol. 64, no. 11, 104341 . https://doi.org/10.1016/j.ejmg.2021.104341

The authors regret that authors list is incomplete The three missing authors that should be placed after Aurelia Poujois: Corinne Collet Department of Biochemistry and Molecular Biology, Lariboisiere University Hospital, APHP, Paris, France corinne.c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pure_au_____::d716cf0c120a49b8a1008a509ba752ac
https://pure.au.dk/portal/da/publications/corrigendum-to-atp7b-variant-spectrum-in-a-french-pediatric-wilson-disease-cohort-eur-j-med-genet-6410-2021-104305-european-journal-of-medical-genetics-2021-6410-s1769721221001713-101016jejmg2021104305(5c52abba-457e-4dab-8b0e-7200feef2081).html

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