Resultados de procura - Stéphane Decramer

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  1. 1
    Consensus recommendations for diagnosis, management and treatment of Fabry disease in paediatric patients

    Consensus recommendations for diagnosis, management and treatment of Fabry disease in paediatric patients por Dominique P. Germain, Alain Fouilhoux, Stéphane Decramer, M. Tardieu, Pascal Pillet, Marc Fila, Serge Rivera, Georges Deschênes, Didier Lacombe

    Publicado 2019
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  2. 2
    Anomalies of the TCF2 Gene Are the Main Cause of Fetal Bilateral Hyperechogenic Kidneys

    Anomalies of the TCF2 Gene Are the Main Cause of Fetal Bilateral Hyperechogenic Kidneys por Stéphane Decramer, Olivier Parant, Sandrine Beaufils, Séverine Clauin, Cécile Guillou, S. Kessler, Jacqueline Aziza, Isabel Bandı́n, Joost P. Schanstra, Christine Bellanné‐Chantelot

    Publicado 2007
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  3. 3
    Congenital ureteropelvic junction obstruction: human disease and animal models

    Congenital ureteropelvic junction obstruction: human disease and animal models por Julie Klein, Julien Gonzalez, Mathieu Miravète, Cécile Caubet, Rana Chaaya, Stéphane Decramer, Isabel Bandı́n, Jean‐Loup Bascands, Bénédicte Buffin‐Meyer, Joost P. Schanstra

    Publicado 2010
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  4. 4
    The HNF1B score is a simple tool to select patients for HNF1B gene analysis

    The HNF1B score is a simple tool to select patients for HNF1B gene analysis por Stanislas Faguer, Nicolas Chassaing, Isabel Bandı́n, Cathie Prouheze, Arnaud Garnier, Audrey Casemayou, Antoine Huart, Joost P. Schanstra, Patrick Calvas, Stéphane Decramer, Dominique Chauveau

    Publicado 2014
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  5. 5
    Spectrum of HNF1B Mutations in a Large Cohort of Patients Who Harbor Renal Diseases

    Spectrum of HNF1B Mutations in a Large Cohort of Patients Who Harbor Renal Diseases por Laurence Heidet, Stéphane Decramer, Audrey Pawtowski, Vincent Morinière, Isabel Bandı́n, Bertrand Knebelmann, Anne-Sophie Lèbre, Stanislas Faguer, Vincent Guigonis, Corinne Antignac, Rémi Salomon

    Publicado 2010
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  6. 6
    Blockade of the Kinin B1 Receptor Ameloriates Glomerulonephritis

    Blockade of the Kinin B1 Receptor Ameloriates Glomerulonephritis por Julie Klein, Julien Gonzalez, Stéphane Decramer, Isabel Bandı́n, Eric Neau, David J. Salant, Peter Heeringa, J. B. Pesquero, Joost P. Schanstra, Jean‐Loup Bascands

    Publicado 2010
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  7. 7
    Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood

    Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood por Stanislas Faguer, Stéphane Decramer, Nicolas Chassaing, Christine Bellanné‐Chantelot, Patrick Calvas, Sandrine Beaufils, Lucie Bessenay, Jean‐Philippe Lengelé, Karine Dahan, Pierre Ronco, Olivier Devuyst, Dominique Chauveau

    Publicado 2011
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  8. 8
    Renal Phenotypes Related to Hepatocyte Nuclear Factor-1β (TCF2) Mutations in a Pediatric Cohort

    Renal Phenotypes Related to Hepatocyte Nuclear Factor-1β (TCF2) Mutations in a Pediatric Cohort por Tim Ulinski, Sandra Lescure, Sandrine Beaufils, Vincent Guigonis, Stéphane Decramer, Denis Morin, Séverine Clauin, Georges DescheCombining Circumflex Accentnes, F Bouissou, A Bensman, Christine Bellanné‐Chantelot

    Publicado 2005
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  9. 9
    Cryptosporidium spp. Infection in Solid Organ Transplantation

    Cryptosporidium spp. Infection in Solid Organ Transplantation por Fanny Lanternier, Karima Amazzough, Loïc Favennec, Marie‐France Mamzer, Hendy Abdoul, Jérôme Tourret, Stéphane Decramer, Julien Zuber, Anne Scemla, Christophe Legendre, Olivier Lortholary, Marie‐Elisabeth Bougnoux

    Publicado 2016
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  10. 10
    Pharmacokinetics of mycophenolate mofetil in children with lupus and clinical findings in favour of therapeutic drug monitoring

    Pharmacokinetics of mycophenolate mofetil in children with lupus and clinical findings in favour of therapeutic drug monitoring por Jean‐Baptiste Woillard, Brigitte Bader‐Meunier, Rémi Salomon, Bruno Ranchin, Stéphane Decramer, Michel Fischbach, E. Bérard, Vincent Guigonis, Jérôme Harambat, Olivier Dunand, Julie Tenenbaum, Pierre Marquet, Franck Saint‐Marcoux

    Publicado 2014
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  11. 11
    Mycophenolic Acid Pharmacokinetics and Relapse in Children with Steroid–Dependent Idiopathic Nephrotic Syndrome

    Mycophenolic Acid Pharmacokinetics and Relapse in Children with Steroid–Dependent Idiopathic Nephrotic Syndrome por Stéphanie Tellier, A. Dallocchio, Vincent Guigonis, F. Saint-Marcoux, Brigitte Llanas, L. Ichay, Isabel Bandı́n, A. Godron, Denis Morin, Karine Brochard, Peggy Gandia, Stéphane Bouchet, Pierre Marquet, Stéphane Decramer, Jérôme Harambat

    Publicado 2016
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  12. 12
    Hepatocyte Nuclear Factor-1β Controls Mitochondrial Respiration in Renal Tubular Cells

    Hepatocyte Nuclear Factor-1β Controls Mitochondrial Respiration in Renal Tubular Cells por Audrey Casemayou, Audren Fournel, Alessia Bagattin, Joost P. Schanstra, Julie Bellière, Stéphane Decramer, Dimitri Marsal, M. Gillet, Nicolas Chassaing, Antoine Huart, Marco Pontoglio, Claude Knauf, Jean‐Loup Bascands, Dominique Chauveau, Stanislas Faguer

    Publicado 2017
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  13. 13
    Nephrin Mutations Can Cause Childhood-Onset Steroid-Resistant Nephrotic Syndrome

    Nephrin Mutations Can Cause Childhood-Onset Steroid-Resistant Nephrotic Syndrome por AureCombining Acute Accentlie Philippe, Fabien Névo, Ernie Esquivel, Dalia Reklaityte, Olivier Gribouval, Marie-JoseCombining Grave Accentphe TeCombining Circumflex Accentte, Chantal Loirat, Jacques Dantal, Michel Fischbach, Claire Pouteil‐Noble, Stéphane Decramer, Martin Hoehne, Thomas Benzing, Marina Charbit, Patrick Niaudet, Corinne Antignac

    Publicado 2008
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  14. 14
    Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome

    Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome por Anne Debost‐Legrand, Cyrielle Tréard, Isabelle Roncelin, Sophie Dreux, Aurélia Bertholet‐Thomas, Françoise Broux, Bruno Daniele, Stéphane Decramer, Georges Deschênes, D. Djeddi, Vincent Guigonis, Nadine Jay, Tackwa Khalifeh, Brigitte Llanas, Denis Morin, G Morin, François Nobili, Christine Piétrement, Amélie Ryckewaert, Rémi Salomon, Isabelle Vrillon, Anne Blanchard, Rosa Vargas‐Poussou

    Publicado 2017
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  15. 15
    Definition, diagnosis and management of fetal lower urinary tract obstruction: consensus of the ERKNet CAKUT-Obstructive Uropathy Work Group

    Definition, diagnosis and management of fetal lower urinary tract obstruction: consensus of the ERKNet CAKUT-Obstructive Uropathy Work Group por Valentina Capone, Nicola Persico, Alfredo Berrettini, Stéphane Decramer, Erika Adalgisa De Marco, Diego De Palma, Alessandra Familiari, Wout Feitz, Maria Herthelius, Vytis Kazlauskas, Max C. Liebau, Gianantonio Manzoni, Michał Maternik, Giovanni Mosiello, Joost P. Schanstra, Johan Vande Walle, Elke Wühl, Elisa Ylinen, Aleksandra Żurowska, Franz Schaefer, Giovanni Montini

    Publicado 2022
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  16. 16
    Clinical characteristics and outcomes of childhood-onset ANCA-associated vasculitis: a French nationwide study

    Clinical characteristics and outcomes of childhood-onset ANCA-associated vasculitis: a French nationwide study por Anne‐Sylvia Sacri, T. Chambaraud, Bruno Ranchin, Benoît Florkin, H. See, Stéphane Decramer, Hugues Flodrops, Tim Ulinski, Emma Allain‐Launay, Olivia Boyer, Olivier Dunand, Michel Fischbach, É. Hachulla, Christine Piétrement, P. Le Pogamp, JL Stéphan, Alexandre Bélot, Hubert Nivet, François Nobili, Loı̈c Guillevin, Pierre Quartier, Georges Deschênes, Rémi Salomon, Marie Essig, J. Harambat

    Publicado 2015
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  17. 17
    Real-world use of complement inhibitors for haemolytic uraemic syndrome: an analysis of the European Rare Kidney Disease Registry cohort

    Real-world use of complement inhibitors for haemolytic uraemic syndrome: an analysis of the European Rare Kidney Disease Registry cohort por Aleksandra Vujović, Anne‐Laure Sellier‐Leclerc, Maria Cristina Mancuso, Olivia Boyer, Atif Awan, Antonio Gargiulo, Sebastian Loos, Marc Fila, Augustina Jankauskiené, Gema Ariceta, Nele Kanzelmeyer, Enrico Vidal, Maria Van Dyck, Tanja Kersnik Levart, N Simánková, Stéphane Decramer, Jonas Hofstetter, Marina Vivarelli, Savino Sciascia, Nicole C. A. J. van de Kar, Franz Schaefer

    Publicado 2025
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  18. 18
    Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease

    Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease por Marie‐Pierre Audrézet, Christine Corbiere, Saïd Lebbah, Vincent Morinière, Françoise Broux, Férielle Louillet, Michel Fischbach, Ariane Zaloszyc, Sylvie Cloarec, Élodie Merieau, Véronique Baudouin, Georges Deschênes, G. Roussey, Sandrine Maestri, Chiara Visconti, Olivia Boyer, Carine Abel, Annie Lahoche, Hanitra Randrianaivo, Lucie Bessenay, Djalila Mekahli, Inès Ouertani, Stéphane Decramer, Amélie Ryckenwaert, Émilie Cornec-Le Gall, Rémi Salomon, Claude Férec, Laurence Heidet

    Publicado 2015
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  19. 19
    CKD and Its Risk Factors among Patients with Cystinuria

    CKD and Its Risk Factors among Patients with Cystinuria por Caroline Prot‐Bertoye, Saïd Lebbah, Michel Daudon, Isabelle Tostivint, Pierre Bataille, Frank Bridoux, Pierre Brignon, Christian Choquenet, Pierre Cochat, Christian Combe, Pierre Conort, Stéphane Decramer, B. Doré, Bertrand Dussol, Marie Essig, Nicolas Gaunez, Dominique Joly, Sophie Le Toquin‐Bernard, Arnaud Méjean, P. Méria, Denis Morin, Hung Viet N’Guyen, Christian Noël, Michel Normand, M. Pietak, Pierre Ronco, C. Saussine, Michel Tsimaratos, Gérard Friedlander, Olivier Traxer, Bertrand Knebelmann, Marie Courbebaisse

    Publicado 2015
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  20. 20
    Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosis

    Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosis por Hélène Louis-Dit-Picard, Ilektra Kouranti, Chloé Rafael, Irmine Ferreira, María Chávez‐Canales, Waed Abdel-Khalek, Eduardo R. Argaiz, Stéphanie Baron, Sarah Vacle, Tiffany Migeon, Richard A. Coleman, Marcio Do Cruzeiro, Marguerite Hureaux, N. Thurairajasingam, Stéphane Decramer, Xavier Girerd, Kevin O’Shaugnessy, Paolo Mulatero, G. Roussey, Ivan Tack, Robert J. Unwin, Rosa Vargas‐Poussou, Olivier Staub, Richard A. Grimm, Paul A. Welling, Gerardo Gamba, Éric Clauser, Juliette Hadchouel, Xavier Jeunemaı̂tre

    Publicado 2020
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