Hasil Pencarian - Stephane Decramer

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  1. 1
    Atypical hemolytic uremic syndrome triggered by varicella infection

    Atypical hemolytic uremic syndrome triggered by varicella infection oleh Pauline Condom, Jean-Michel Mansuy, Stéphane Decramer, Jacques Izopet, Catherine Mengelle

    Diterbitkan 2017-01-01
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  2. 2
    Unusual fetal ascites and spontaneous bladder rupture in a female fetus: a case report

    Unusual fetal ascites and spontaneous bladder rupture in a female fetus: a case report oleh Florence Cadoret, Edith Brazet, Agnès Sartor, Isabelle Lacroix, Charlotte Casper, Stéphane Decramer, Olivier Parant

    Diterbitkan 2020-07-01
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  3. 3
    Comparison of the amniotic fluid and fetal urine peptidome for biomarker discovery in renal developmental disease

    Comparison of the amniotic fluid and fetal urine peptidome for biomarker discovery in renal developmental disease oleh Camille Fédou, Benjamin Breuil, Igor Golovko, Stéphane Decramer, Pedro Magalhães, Françoise Muller, Sophie Dreux, Petra Zürbig, Julie Klein, Joost P. Schanstra, Bénédicte Buffin-Meyer

    Diterbitkan 2020-12-01
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  4. 4
    Valganciclovir is not associated with decreased EBV infection rate in pediatric kidney transplantation

    Valganciclovir is not associated with decreased EBV infection rate in pediatric kidney transplantation oleh 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

    Diterbitkan 2023-01-01
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  5. 5
    National survey of prevention and management of CMV infection in pediatric kidney transplantation in comparison to clinical practice guidelines

    National survey of prevention and management of CMV infection in pediatric kidney transplantation in comparison to clinical practice guidelines oleh 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

    Diterbitkan 2022-12-01
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  6. 6
    The European Rare Kidney Disease Registry (ERKReg): objectives, design and initial results

    The European Rare Kidney Disease Registry (ERKReg): objectives, design and initial results oleh 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

    Diterbitkan 2021-06-01
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  7. 7
    Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome

    Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome oleh 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

    Diterbitkan 2019-09-01
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