Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jill Serre"'
Autor:
Solenne Le Louet, Véronique Icart, Marion Strullu, Arnaud Petit, Claire Freycon, Pascale Blouin, Jill Serre, Nicolas Rama, Yves Reguerre, Christophe Piguet, Marlène Pasquet, Audrey David, Pauline Simon, Marilyne Poiree, Liana Carausu, Fanny Rialland, Wadih Abouchahla, Paul Saultier, Stéphane Ducassou, Julie Valduga, André Baruchel, Yves Bertrand, Carine Domenech
Publikováno v:
Journal of Cancer. 13:1272-1281
Ten to fifteen percent of children with acute lymphoblastic leukemia (ALL) relapse following treatment. Of these, less than 2% display ophthalmic relapses, which owing to their scarcity, are largely undocumented, leaving clinicians with few diagnosti
Autor:
Cyrus Chargari, Christine Haie-Meder, Sophie Espenel, Max-Adrien Garcia, Myriam Ben-Arush, Stéphanie Bolle, Anna Borjesson, Maja Cesen, Rita Costa Lago, Anne-Sophie Defachelles, Barbara De Moerloose, Christine Devalck, Pernille Edslev, Nuno Jorge Farinha, Nadine Francotte, Heidi Glosli, Sebastien Gouy, Gabriela Guillen Burrieza, Sylvie Helfre, Sabine Irtan, Antonis Kattamis, Ana Lacerda, Antonin Levy, Lisa Lyngsie Hjalgrim, Ludovic Mansuy, Eric Mascard, Salma Moalla, Daniel Orbach, Cormac Owens, Pascale Philippe-Chomette, Barry Pizer, Claire Pluchart, Marleen Renard, Anne Gro Wesenberg Rognlien, Angélique Rome, Sabine Sarnacki, Akmal Safwat, Amalia Schiavetti, Jill Serre, Cécile Verite, Nicolas Von Der Weid, Mariusz Wysocki, Dominique Valteay-Couanet, Eric Deutsch, Véronique Minard-Colin, Hélène Martelli, Florent Guérin
Publikováno v:
Chargari, C, Haie-Meder, C, Espenel, S, Garcia, M A, Ben-Arush, M, Bolle, S, Borjesson, A, Cesen, M, Lago, R C, Defachelles, A S, De Moerloose, B, Devalck, C, Edslev, P, Farinha, N J, Francotte, N, Glosli, H, Gouy, S, Burrieza, G G, Helfre, S, Irtan, S, Kattamis, A, Lacerda, A, Levy, A, Hjalgrim, L L, Mansuy, L, Mascard, E, Moalla, S, Orbach, D, Owens, C, Philippe-Chomette, P, Pizer, B, Pluchart, C, Renard, M, Rognlien, A G W, Rome, A, Sarnacki, S, Safwat, A, Schiavetti, A, Serre, J, Verite, C, Weid, N V D, Wysocki, M, Valteay-Couanet, D, Deutsch, E, Minard-Colin, V, Martelli, H & Guérin, F 2022, ' Brachytherapy for Pediatric Patients at Gustave Roussy Cancer Campus : A Model of International Cooperation for Highly Specialized Treatments ', International Journal of Radiation Oncology Biology Physics, vol. 113, no. 3, pp. 602-613 . https://doi.org/10.1016/j.ijrobp.2022.03.003
Purpose: Childhood cancer is rare, and treatment is frequently associated with long-term morbidity. Disparities in survival and long-term side effects encourage the establishment of networks to increase access to complex organ-conservative strategies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::757eb0c5e39516c2c77ee52225e9c01a
https://pure.au.dk/portal/da/publications/brachytherapy-for-pediatric-patients-at-gustave-roussy-cancer-campus(6038619d-ae42-4946-9454-5ad90f27ce31).html
https://pure.au.dk/portal/da/publications/brachytherapy-for-pediatric-patients-at-gustave-roussy-cancer-campus(6038619d-ae42-4946-9454-5ad90f27ce31).html
Autor:
Maria Veiga-da-Cunha, Aline Vincent, Jérémie Rosain, Martin Castelle, Jill Serre, Laurent Renesme, Valérie Cormier-Daire, Takfarinas Kentache, Benjamin Fournier, Sophie Blesson, Nathalie Aladjidi, Despina Moshous, Mathieu Fusaro, Eulalie Lasseaux, Capucine Picard, Fanny Morice Picard, Nathalie Seta, Bénédicte Neven, Anne-Lise Delezoide, Catherine Fallet-Bianco, Emile Van Schaftingen
Publikováno v:
Journal of clinical immunology, Vol. 41, no. 5, p. 958-966 (2021)
Phosphoglucomutase 3 (PGM3) deficiency is a rare congenital disorder of glycosylation. Most of patients with autosomal recessive hypomorphic mutations in PGM3 encoding for phosphoglucomutase 3 present with eczema, skin and lung infections, elevated s