Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Robert Novo"'
Autor:
Elodie Cheyssac, Hamidou Savadogo, Nathan Lagoutte, Véronique Baudouin, Marina Charbit, Robert Novo, Anne-Laure Sellier-Leclerc, Marc Fila, Stéphane Decramer, Elodie Merieau, Ariane Zaloszyc, Jérôme Harambat, Gwenaelle Roussey
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2023)
IntroductionPrimary infection or reactivation of Epstein-Barr Virus (EBV) is a significant cause of morbidity and mortality in pediatric kidney transplantation. Valganciclovir (VGC) treatment is recommended for prophylaxis of cytomegalovirus infectio
Externí odkaz:
https://doaj.org/article/8166121861074e26ae5ff5ce788f395b
Autor:
Iona Madden, Véronique Baudouin, Marina Charbit, Bruno Ranchin, Gwenaëlle Roussey, Robert Novo, Florentine Garaix, Stéphane Decramer, Marc Fila, Elodie Merieau, Isabelle Vrillon, Ariane Zaloszyc, Julien Hogan, Jérôme Harambat
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundCytomegalovirus (CMV) is one of the most frequent opportunistic infections in kidney transplant (KT) recipients and is a risk factor for patient and graft survival after KT. Center-to-center variation, optimal prevention and treatment strat
Externí odkaz:
https://doaj.org/article/8a03648a09b94c63951c62186d9ce4bd
Autor:
Christelle Arrondel, Sophia Missoury, Rozemarijn Snoek, Julie Patat, Giulia Menara, Bruno Collinet, Dominique Liger, Dominique Durand, Olivier Gribouval, Olivia Boyer, Laurine Buscara, Gaëlle Martin, Eduardo Machuca, Fabien Nevo, Ewen Lescop, Daniela A. Braun, Anne-Claire Boschat, Sylvia Sanquer, Ida Chiara Guerrera, Patrick Revy, Mélanie Parisot, Cécile Masson, Nathalie Boddaert, Marina Charbit, Stéphane Decramer, Robert Novo, Marie-Alice Macher, Bruno Ranchin, Justine Bacchetta, Audrey Laurent, Sophie Collardeau-Frachon, Albertien M. van Eerde, Friedhelm Hildebrandt, Daniella Magen, Corinne Antignac, Herman van Tilbeurgh, Géraldine Mollet
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-13 (2019)
The biosynthesis of N6-threonylcarbamoylated adenosine 37 in tRNA (t6A) involves the YRDC enzyme and the KEOPS complex. Here, the authors report mutations in YRDC and the KEOPS component GON7 in Galloway-Mowat syndrome and determine the crystal struc
Externí odkaz:
https://doaj.org/article/77cd12b7d5974fda8810f1a228293257
Autor:
Bénédicte Driollet, Florian Bayer, Theresa Kwon, Saoussen Krid, Bruno Ranchin, Michel Tsimaratos, Cyrielle Parmentier, Robert Novo, Gwenaelle Roussey, Stéphanie Tellier, Marc Fila, Ariane Zaloszyc, Astrid Godron-Dubrasquet, Sylvie Cloarec, Isabelle Vrillon, Françoise Broux, Etienne Bérard, Sophie Taque, Christine Pietrement, François Nobili, Vincent Guigonis, Ludivine Launay, Cécile Couchoud, Jérôme Harambat, Karen Leffondré
Publikováno v:
Kidney International Reports
Kidney International Reports, 2021, 11p. ⟨10.1016/j.ekir.2021.12.015⟩
Kidney International Reports, 2021, 11p. ⟨10.1016/j.ekir.2021.12.015⟩
International audience; IntroductionSocioeconomic status (SES) is recognized as an important determinant of kidney health. We aimed to evaluate the association of social deprivation with different indicators at kidney replacement therapy (KRT) initia
Publikováno v:
médecine/sciences. 38:182-190
Pour un jeune adulte atteint d’une maladie chronique, le passage de la médecine pédiatrique à la médecine pour adultes est une étape délicate, avec un risque élevé de mauvaise adhésion thérapeutique et de perte de suivi, dont les conséqu
Autor:
Robert Novo, Fitsum Guebre-Egziabher, Loïc De Parscau, Aurélia Bertholet-Thomas, Marie Essig, Gérard Champion, Aude Servais, Pierre Cochat, Jennifer Radenac, Anne-Laure Leclerc, Véronique Baudouin, Olivier Dunand, Nathalie Buebuyck, Béatrice Sartoris, Béatrice Langellier-Bellevue, Justine Perrin, Marina Charbit, Dominique Rousiot, Stéphane Burtey, Bruno Moulin, Françoise Broux, Sandrine Lemoine, Yahsou Delmas, Stéphanie Belaiche, Elodie Merieau, Arvind Nagra
Publikováno v:
Néphrologie & Thérapeutique. 17:137-142
Resume Des recommandations specifiques a la nephrologie ont ete redigees sous l’egide de l’Association internationale de nephrologie pediatrique en 2011. Ces recommandations preconisent une transition individualisee, debutant entre 12 et 14 ans,
Publikováno v:
Medecine sciences : M/S. 38(2)
For a young patient suffering from a chronic disease, the transition from pediatric to adult care unit is a tricky step, with a high risk of poor therapeutic compliance, loss of follow-up, and possibly tragic consequences. Better knowledge of these r
Autor:
Koenraad Veys, Ward Zadora, Katharina Hohenfellner, Detlef Bockenhauer, Mirian C. H. Janssen, Patrick Niaudet, Aude Servais, Rezan Topaloglu, Martine Besouw, Robert Novo, Dieter Haffner, Nele Kanzelmeyer, Lars Pape, Elke Wühl, Erik Harms, Atif Awan, Przemyslaw Sikora, Gema Ariceta, Bert van den Heuvel, Elena Levtchenko
Publikováno v:
Journal of Inherited Metabolic Disease, 46(1), 43-54. SPRINGER
Journal of Inherited Metabolic Disease, 46, 43-54
Journal of Inherited Metabolic Disease, 46, 1, pp. 43-54
Journal of Inherited Metabolic Disease, 46, 43-54
Journal of Inherited Metabolic Disease, 46, 1, pp. 43-54
Item does not contain fulltext Infantile nephropathic cystinosis (INC) is an inheritable lysosomal storage disorder characterized by lysosomal cystine accumulation, progressive kidney disease, and multiple extrarenal complications (ERCs). Cysteamine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba33b07032701bbc050a61345df468c8
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85139213892
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85139213892
Autor:
Marcella Greco, Detlef Bockenhauer, Jun Oh, Corinne Antignac, Elena Levtchenko, Fatih Ozaltin, Katharina Hohenfellner, Rezan Topaloglu, Gema Ariceta, Aude Servais, Aurélia Bertholet-Thomas, Suzanne Collin, Robert Novo, Olivier Devuyst, Lucilla Ravà, Francesco Emma, Sally A. Hulton, Mirian C. H. Janssen, Koenraad Veys, Lars Pape, Elisabeth A.M. Cornelissen, Chiara Bettini, William van’t Hoff, Patrick Niaudet, Dieter Haffner, Georges Deschênes
Publikováno v:
Kidney International, 100, 1112-1123
Kidney International, 100, 5, pp. 1112-1123
Kidney International, 100, 5, pp. 1112-1123
Nephropathic cystinosis is a rare disease secondary to recessive mutations of the CTNS gene encoding the lysosomal cystine transporter cystinosin, causing accumulation of cystine in multiple organs. Over the years, the disease has evolved from being
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45837aebe780053fed9778740926d177
https://doi.org/10.5167/uzh-206338
https://doi.org/10.5167/uzh-206338
Autor:
Corinne Alberti, Paula Vieira-Martins, Véronique Frémeaux-Bacchi, Anne-Laure Sellier-Leclerc, Patricia Mariani, Tim Ulinski, Georges Deschênes, Sophie Limou, Annie Lahoche, Gwenaelle Roussey, François Nobili, Mathilde Cailliez, Brigitte Llanas, Theresa Kwon, Robert Novo, François-Xavier Weill, Chantal Loirat
Publikováno v:
Clinical Journal of the American Society of Nephrology
Clinical Journal of the American Society of Nephrology, American Society of Nephrology, 2019, 14 (3), pp.364-377. ⟨10.2215/CJN.05830518⟩
Clinical Journal of the American Society of Nephrology, 2019, 14 (3), pp.364-377. ⟨10.2215/CJN.05830518⟩
Clinical Journal of the American Society of Nephrology, American Society of Nephrology, 2019, 14 (3), pp.364-377. ⟨10.2215/CJN.05830518⟩
Clinical Journal of the American Society of Nephrology, 2019, 14 (3), pp.364-377. ⟨10.2215/CJN.05830518⟩
International audience; BACKGROUND AND OBJECTIVES: Inherited complement hyperactivation is critical for the pathogenesis of atypical hemolytic uremic syndrome (HUS) but undetermined in postdiarrheal HUS. Our aim was to investigate complement activati