Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Stèphane Decramer"'
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:
Giulia Bassanese, Tanja Wlodkowski, Aude Servais, Laurence Heidet, Dario Roccatello, Francesco Emma, Elena Levtchenko, Gema Ariceta, Justine Bacchetta, Giovambattista Capasso, Augustina Jankauskiene, Marius Miglinas, Pietro Manuel Ferraro, Giovanni Montini, Jun Oh, Stephane Decramer, Tanja Kersnik Levart, Jack Wetzels, Elisabeth Cornelissen, Olivier Devuyst, Aleksandra Zurowska, Lars Pape, Anja Buescher, Dieter Haffner, Natasa Marcun Varda, Gian Marco Ghiggeri, Giuseppe Remuzzi, Martin Konrad, Germana Longo, Detlef Bockenhauer, Atif Awan, Ilze Andersone, Jaap W. Groothoff, Franz Schaefer
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-15 (2021)
Abstract Background The European Rare Kidney Disease Reference Network (ERKNet) recently established ERKReg, a Web-based registry for all patients with rare kidney diseases. The main objectives of this core registry are to generate epidemiological in
Externí odkaz:
https://doaj.org/article/298d7b2d56344d9ab3fa1ca68f07142f
Autor:
Camille Fédou, Benjamin Breuil, Igor Golovko, Stéphane Decramer, Pedro Magalhães, Françoise Muller, Sophie Dreux, Petra Zürbig, Julie Klein, Joost P. Schanstra, Bénédicte Buffin-Meyer
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-9 (2020)
Abstract Production of amniotic fluid (AF) is view as predominately driven by excretion of fetal urine (FU). However, the origin of AF peptides, often considered as potential biomarkers of developmental diseases, has never been investigated. Here, we
Externí odkaz:
https://doaj.org/article/428622a5f2e3402e83de58ba284e7d13
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
Publikováno v:
IDCases, Vol 9, Iss C, Pp 89-90 (2017)
Varicella Zoster Virus (VZV) is a well-known virus that belongs to the Herpesviridae family which induces a self-limited disease except in specific cases in particular among stem cell transplant patients. This virus is not known however to trigger at
Externí odkaz:
https://doaj.org/article/23adad22f298438599cd361c27bd1734
Autor:
Valentina Capone, Nicola Persico, Alfredo Berrettini, Stèphane Decramer, Erika Adalgisa De Marco, Diego De Palma, Alessandra Familiari, Wout Feitz, Maria Herthelius, Vytis Kazlauskas, Max Liebau, Gianantonio Manzoni, Michal Maternik, Giovanni Mosiello, Joost Peter Schanstra, Johan Vande Walle, Elke Wühl, Elisa Ylinen, Aleksandra Zurowska, Franz Schaefer, Giovanni Montini
Publikováno v:
Nature Reviews. Urology, 19, 295-303
Nature Reviews. Urology, 19, 5, pp. 295-303
Nature Reviews. Urology, 19, 5, pp. 295-303
Contains fulltext : 251790.pdf (Publisher’s version ) (Closed access) Fetal lower urinary tract obstruction (LUTO) is associated with high mortality and postnatal morbidity caused by lung hypoplasia and impaired kidney function. Specific diagnostic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::febe920a613bfd2b3ecedb62e6dd6ea4
http://hdl.handle.net/2066/251790
http://hdl.handle.net/2066/251790
Autor:
Florence Cadoret, Edith Brazet, Agnès Sartor, Isabelle Lacroix, Charlotte Casper, Stéphane Decramer, Olivier Parant
Publikováno v:
Journal of Medical Case Reports, Vol 14, Iss 1, Pp 1-5 (2020)
Abstract Background Fetal bladder rupture causing urinary ascites is uncommon. It is generally related to invasive fetal medicine procedures or obstructive disorders such as in posterior urethral valves in male fetuses. An exceptional case of spontan
Externí odkaz:
https://doaj.org/article/dfd0214e261a45558ed4e277005c6bc2
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