Zobrazeno 1 - 10
of 154
pro vyhledávání: '"Christophe, Chardot"'
Autor:
Amélie Roehrig, Theo Z. Hirsch, Aurore Pire, Guillaume Morcrette, Barkha Gupta, Charles Marcaillou, Sandrine Imbeaud, Christophe Chardot, Emmanuel Gonzales, Emmanuel Jacquemin, Masahiro Sekiguchi, Junko Takita, Genta Nagae, Eiso Hiyama, Florent Guérin, Monique Fabre, Isabelle Aerts, Sophie Taque, Véronique Laithier, Sophie Branchereau, Catherine Guettier, Laurence Brugières, Brice Fresneau, Jessica Zucman-Rossi, Eric Letouzé
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-18 (2024)
Abstract Hepatoblastomas (HB) display heterogeneous cellular phenotypes that influence the clinical outcome, but the underlying mechanisms are poorly understood. Here, we use a single-cell multiomic strategy to unravel the molecular determinants of t
Externí odkaz:
https://doaj.org/article/14c4d115a5e440889f8a8405c0ba7b92
Autor:
Jill Pilet, Theo Z. Hirsch, Barkha Gupta, Amélie Roehrig, Guillaume Morcrette, Aurore Pire, Eric Letouzé, Brice Fresneau, Sophie Taque, Laurence Brugières, Sophie Branchereau, Christophe Chardot, Isabelle Aerts, Sabine Sarnacki, Monique Fabre, Catherine Guettier, Sandra Rebouissou, Jessica Zucman-Rossi
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-14 (2023)
Abstract Pediatric liver tumors are very rare tumors with the most common diagnosis being hepatoblastoma. While hepatoblastomas are predominantly sporadic, around 15% of cases develop as part of predisposition syndromes such as Beckwith-Wiedemann (11
Externí odkaz:
https://doaj.org/article/b855b46d29ee498d9b652b37172ee706
Autor:
Baudouin Denis de Senneville, Fatma Zohra Khoubai, Marc Bevilacqua, Alexandre Labedade, Kathleen Flosseau, Christophe Chardot, Sophie Branchereau, Jean Ripoche, Stefano Cairo, Etienne Gontier, Christophe F. Grosset
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-10 (2021)
de Senneville et al. demonstrate an integrated workflow combining 3D imaging, manual and machine learning-based semi-automatic segmentation, mathematics and infographics to study the spatial organization of patient-derived hepatoblastoma xenograft ti
Externí odkaz:
https://doaj.org/article/29e44149c9914d8fa417f17a2e6704ae
Autor:
Caroline de Gouveia Buff Passone, Gaëlle Vermillac, Willem Staels, Alix Besancon, Dulanjalee Kariyawasam, Cécile Godot, Cécile Lambe, Cécile Talbotec, Muriel Girard, Christophe Chardot, Laureline Berteloot, Taymme Hachem, Alexandre Lapillonne, Amélie Poidvin, Caroline Storey, Mathieu Neve, Cosmina Stan, Emmanuelle Dugelay, Anne-Laure Fauret-Amsellem, Yline Capri, Hélène Cavé, Marina Ybarra, Vikash Chandra, Raphaël Scharfmann, Elise Bismuth, Michel Polak, Jean Claude Carel, Bénédicte Pigneur, Jacques Beltrand
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Aims/HypothesisCaused by biallelic mutations of the gene encoding the transcription factor RFX6, the rare Mitchell–Riley syndrome (MRS) comprises neonatal diabetes, pancreatic hypoplasia, gallbladder agenesis or hypoplasia, duodenal atresia, and se
Externí odkaz:
https://doaj.org/article/0415565a92324913891728b1437cc6c5
Autor:
Caroline P. Lemoine, Omid Madadi-Sanjani, Claus Petersen, Christophe Chardot, Jean de Ville de Goyet, Riccardo Superina
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 9, p 3229 (2023)
Background: Pediatric liver surgery is a complex and challenging procedure and can be associated with major complications, including mortality. Best practices are not established. The aims of this study were to evaluate surgeons’ individual and ins
Externí odkaz:
https://doaj.org/article/58040fc35eef4f28b540b70c3771cfac
Autor:
Mark Davenport, Omid Madadi-Sanjani, Christophe Chardot, Henkjan J. Verkade, Saul J. Karpen, Claus Petersen
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 21, p 6601 (2022)
Biliary atresia, a fibro-obliterative disease of the newborn, is usually initially treated by Kasai portoenterostomy, although there are many variations in technique and different options for post-operative adjuvant medical therapy. A questionnaire o
Externí odkaz:
https://doaj.org/article/52a82534b34f4407aa52979325303ba0
Autor:
Jean de Ville de Goyet, Toni Illhardt, Christophe Chardot, Peace N. Dike, Ulrich Baumann, Katherine Brandt, Barbara E. Wildhaber, Mikko Pakarinen, Fabrizio di Francesco, Ekkehard Sturm, Marianna Cornet, Caroline Lemoine, Eva Doreen Pfister, Ana M. Calinescu, Maria Hukkinen, Sanjiv Harpavat, Fabio Tuzzolino, Riccardo Superina
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 8, p 2142 (2022)
Background & Aims: Biliary atresia (BA) is the commonest single etiology indication for liver replacement in children. As timely access to liver transplantation (LT) remains challenging for small BA children (with prolonged waiting time being associa
Externí odkaz:
https://doaj.org/article/6eb98cc1f93c45669b8db2eff3baa51e
Autor:
Florian, Seckler, Célia, Turco, Kayvan, Mohkam, Pietro, Addeo, Fabien, Robin, François, Cauchy, Charlotte, Maulat, Raffaele, Brustia, Brice, Paquette, François, Faitot, Delphine, Weil Verhoeven, Anne, Minello, Zaher, Lakkis, Vincent, Di Martino, Marianne, Latournerie, Laurence, Chiche, Mehdi, El Amrani, Petru, Bucur, Francis, Navarro, Sophie, Chopinet, Mircea, Chirica, Johan, Gagnière, Antonio, Iannelli, Gaëlle, Cheisson, Christophe, Chardot, Daniele, Sommacale, Fabrice, Muscari, Federica, Dondero, Laurent, Sulpice, Philippe, Bachellier, Olivier, Scatton, Jean Yves, Mabrut, Bruno, Heyd, Alexandre, Doussot
Publikováno v:
Transplantation. 107:664-669
In the current setting of organ shortage, brain-dead liver donors with recent liver trauma (RLT) represent a potential pool of donors. Yet, data on feasibility and safety of liver transplantation (LT) using grafts with RLT are lacking.All liver graft
Autor:
Alastair Baker, Esteban Frauca Remacha, Juan Torres Canizales, Luz Yadira Bravo-Gallego, Emer Fitzpatrick, Angel Alonso Melgar, Gema Muñoz Bartolo, Luis Garcia Guereta, Esther Ramos Boluda, Yasmina Mozo, Dorota Broniszczak, Wioletta Jarmużek, Piotr Kalicinski, Britta Maecker-Kolhoff, Julia Carlens, Ulrich Baumann, Charlotte Roy, Christophe Chardot, Elisa Benetti, Mara Cananzi, Elisabetta Calore, Luca Dello Strologo, Manila Candusso, Maria Francelina Lopes, Manuel João Brito, Cristina Gonçalves, Carmen Do Carmo, Xavier Stephenne, Lars Wennberg, Rosário Stone, Jelena Rascon, Caroline Lindemans, Dominik Turkiewicz, Eugenia Giraldi, Emanuele Nicastro, Lorenzo D’Antiga, Oanez Ackermann, Paloma Jara Vega
Publikováno v:
Children, Vol 8, Iss 8, p 661 (2021)
(1) Background: Post-transplant lymphoproliferative disease (PTLD) is a significant complication of solid organ transplantation (SOT). However, there is lack of consensus in PTLD management. Our aim was to establish a present benchmark for comparison
Externí odkaz:
https://doaj.org/article/e4cb0f49cb584054a82941ab9f84d7ba
Autor:
Guillaume Morcrette, Theo Z Hirsch, Elise Badour, Jill Pilet, Stefano Caruso, Julien Calderaro, Yoann Martin, Sandrine Imbeaud, Eric Letouzé, Sandra Rebouissou, Sophie Branchereau, Sophie Taque, Christophe Chardot, Catherine Guettier, Jean-Yves Scoazec, Monique Fabre, Laurence Brugières, Jessica Zucman-Rossi
Publikováno v:
OncoImmunology, Vol 8, Iss 6 (2019)
Hepatoblastoma (HB) is the most common liver cancer in children. We aimed to characterize HB related to APC (Adenomatous Polyposis Coli) germline mutation (APC-HB). This French multicentric retrospective study included 12 APC-HB patients under 5 at d
Externí odkaz:
https://doaj.org/article/76d10b2eed8042af9fde5d21abf7f106