Rezultaty - Hubert Nivet

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  1. 1
    Kidney damage due to tuberous sclerosis complex: Management recommendations

    Kidney damage due to tuberous sclerosis complex: Management recommendations od Olivier Rouvière, Hubert Nivet, N. Grenier, Luca Zini, É. Lechevallier

    Wydane 2013
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    Artigo
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  2. 2
    Effects of current smoking and smoking discontinuation on renal function and proteinuria in the general population

    Effects of current smoking and smoking discontinuation on renal function and proteinuria in the general population od Jean‐Michel Halimi, Bruno Giraudeau, Sylviane Vol, E Cacès, Hubert Nivet, Yvon Lebranchu, Jean Tichet

    Wydane 2000
    Dokumenty pełnotekstowe
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  3. 3
    How artificial intelligence improves radiological interpretation in suspected pulmonary embolism

    How artificial intelligence improves radiological interpretation in suspected pulmonary embolism od A. Ben Cheikh, G. Gorincour, Hubert Nivet, Julien May, Mylène Seux, Paul Calame, Vivien Thomson, Éric Delabrousse, Amandine Crombé

    Wydane 2022
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  4. 4
    Occupational exposure in ANCA-positive patients: A case-control study

    Occupational exposure in ANCA-positive patients: A case-control study od Séverine Beaudreuil, Gérard Lasfargues, Laurence Lauériere, Zen El Ghoul, Florence Fourquet, Cédric Longuet, Jean‐Michel Halimi, Hubert Nivet, Matthias Büchler

    Wydane 2005
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  5. 5
    Anti–Factor H Autoantibodies Associated with Atypical Hemolytic Uremic Syndrome

    Anti–Factor H Autoantibodies Associated with Atypical Hemolytic Uremic Syndrome od Marie‐Agnès Dragon‐Durey, Chantal Loirat, Sylvie Cloarec, Marie-Alice Macher, Jacques Blouin, Hubert Nivet, Laurence Weiss, Wolf H. Fridman, Véronique Frémeaux‐Bacchi

    Wydane 2004
    Dokumenty pełnotekstowe
    Artigo
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  6. 6
    Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus

    Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus od Erik‐Jan Kamsteeg, Daniel G. Bichet, Irene B. M. Konings, Hubert Nivet, Michelle Lonergan, Marie‐Françoise Arthus, C.H. van Os, Peter M.T. Deen

    Wydane 2003
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  7. 7
    Early Pulse Pressure and Low-Grade Proteinuria as Independent Long-Term Risk Factors for New-Onset Diabetes Mellitus After Kidney Transplantation

    Early Pulse Pressure and Low-Grade Proteinuria as Independent Long-Term Risk Factors for New-Onset Diabetes Mellitus After Kidney Transplantation od M. Roland, Philippe Gatault, A. Al-Najjar, Claire Doute, Isabelle Barbet, Valérie Châtelet, J. Marlière, Hubert Nivet, M.W. Büchler, Yvon Lebranchu, J.M. Halimi, I. Laouad

    Wydane 2008
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  8. 8
    Focal scar and diffuse myocardial fibrosis are independent imaging markers in repaired tetralogy of Fallot

    Focal scar and diffuse myocardial fibrosis are independent imaging markers in repaired tetralogy of Fallot od Hubert Cochet, Xavier Iriart, Antoine Allain-Nicolaï, Claudia Camaioni, Soumaya Sridi, Hubert Nivet, Emmanuelle Fournier, Marie–Lou Dinet, Zakaria Jalal, François Laurent, Michel Montaudon, Jean‐Benoît Thambo

    Wydane 2019
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  9. 9
    High-Resolution Late Gadolinium Enhancement Magnetic Resonance for the Diagnosis of Myocardial Infarction With Nonobstructed Coronary Arteries

    High-Resolution Late Gadolinium Enhancement Magnetic Resonance for the Diagnosis of Myocardial Infarction With Nonobstructed Coronary Arteries od Pierre-François Lintingre, Hubert Nivet, Stéphanie Clément-Guinaudeau, Claudia Camaioni, Soumaya Sridi, O. Corneloup, Édouard Gerbaud, Pierre Coste, Gaël Dournes, V. Latrabe, François Laurent, Michel Montaudon, Hubert Cochet

    Wydane 2020
    Dokumenty pełnotekstowe
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  10. 10
    OCT and CMR for the Diagnosis of Patients Presenting With MINOCA and Suspected Epicardial Causes

    OCT and CMR for the Diagnosis of Patients Presenting With MINOCA and Suspected Epicardial Causes od Édouard Gerbaud, Fabien Arabucki, Hubert Nivet, Christophe Barbey, Laura Cetran, Stéphan Chassaing, Benjamin Séguy, Arnaud Lesimple, Hubert Cochet, Michel Montaudon, François Laurent, Olivier Bar, Guillermo J. Tearney, Pierre Coste

    Wydane 2020
    Dokumenty pełnotekstowe
    Artigo
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  11. 11
    Death after withdrawal from dialysis: the most common cause of death in a French dialysis population

    Death after withdrawal from dialysis: the most common cause of death in a French dialysis population od Béatrice Birmelé, François Mullier, J Pengloan, Patrick Français, Didier Testou, G Brillet, D. Lechapois, S. Baudin, O. Grézard, Jean-Louis Jourdan, M. Fodil-Cherif, Mona Abaza, L Dupouet, Gilles Fournier, Hubert Nivet

    Wydane 2004
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  12. 12
    Mutations of NPHP2 and NPHP3 in infantile nephronophthisis

    Mutations of NPHP2 and NPHP3 in infantile nephronophthisis od Kálmán Tory, Caroline Rousset‐Rouvière, Marie‐Claire Gubler, Vincent Morinière, Audrey Pawtowski, C. Becker, C. Guyot, Sophie Gié, Yaacov Frishberg, Hubert Nivet, Georges Deschênes, Pierre Cochat, Marie‐France Gagnadoux, Sophie Saunier, Corinne Antignac, Rémi Salomon

    Wydane 2009
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  13. 13
    Genotype–phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome

    Genotype–phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome od Jérôme Harambat, Sonia Fargue, Cécile Acquaviva, Marie‐France Gagnadoux, Françoise Janssen, A. Liutkus, Chebl Mourani, Marie‐Alice Macher, Daniel Abramowicz, Christophe Legendre, Antoine Dürrbach, Michel Tsimaratos, Hubert Nivet, Éric Girardin, Anne‐Marie Schott, Marie-Odile Rolland, Pierre Cochat

    Wydane 2009
    Dokumenty pełnotekstowe
    Artigo
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  14. 14
    Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1

    Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1 od Sonia Fargue, Jérôme Harambat, Marie‐France Gagnadoux, Michel Tsimaratos, Françoise Janssen, Brigitte Llanas, Jean-Pierre Berthélémé, B. Boudailliez, Gérard Champion, C. Guyot, Marie‐Alice Macher, Hubert Nivet, Bruno Ranchin, Rémi Salomon, Sophie Taque, Marie-Odile Rolland, Pierre Cochat

    Wydane 2009
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  15. 15
    Differential Impact of Complement Mutations on Clinical Characteristics in Atypical Hemolytic Uremic Syndrome

    Differential Impact of Complement Mutations on Clinical Characteristics in Atypical Hemolytic Uremic Syndrome od Anne‐Laure Sellier‐Leclerc, Véronique Frémeaux‐Bacchi, Marie‐Agnès Dragon‐Durey, Marie-Alice Macher, Patrick Niaudet, Geneviève Guest, B. Boudailliez, F Bouissou, Georges Deschênes, Sophie Gié, Michel Tsimaratos, Michel Fischbach, Denis Morin, Hubert Nivet, Corinne Alberti, Chantal Loirat

    Wydane 2007
    Dokumenty pełnotekstowe
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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 od 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

    Wydane 2015
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  17. 17
    Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination

    Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination od Edgar A. Otto, Bernhard Schermer, Tomoko Obara, John F. O’Toole, Karl S. Hiller, Adelheid M. Mueller, Rainer Ruf, Julia Hoefele, Frank Beekmann, Daniel Landau, John W. Foreman, Judith A. Goodship, Tom Strachan, Andreas Kispert, Matthias T. F. Wolf, M. F. Gagnadoux, Hubert Nivet, Corinne Antignac, Gerd Walz, Iain A. Drummond, Thomas Benzing, Friedhelm Hildebrandt

    Wydane 2003
    Dokumenty pełnotekstowe
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  18. 18
    Spectrum of Mutations in Gitelman Syndrome

    Spectrum of Mutations in Gitelman Syndrome od Rosa Vargas‐Poussou, Karin Dahan, Diana Kahila, Annabelle Vénisse, Eva Riveira‐Muñoz, Huguette Debaix, Bernard Grisart, Frank Bridoux, Robert J. Unwin, Bruno Moulin, Jean‐Philippe Haymann, Marie‐Christine Vantyghem, Claire Rigothier, Bertrand Dussol, M. Godin, Hubert Nivet, Laurence Dubourg, Ivan Tack, Anne‐Paule Gimenez‐Roqueplo, Pascal Houillier, Anne Blanchard, Olivier Devuyst, Xavier Jeunemaı̂tre

    Wydane 2011
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  19. 19
    Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome

    Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome od Véronique Frémeaux‐Bacchi, Elizabeth C. Miller, M. Kathryn Liszewski, Lisa Strain, Jacques Blouin, Alison L. Brown, Nadeem Moghal, Bernard S. Kaplan, Robert A. Weiss, Karl Lhotta, Gaurav Kapur, Tej K. Mattoo, Hubert Nivet, William Wong, Sophie Gié, Bruno Hurault de Ligny, Michel Fischbach, Ritu Gupta, Richard E. Hauhart, Vincent Meunier, Chantal Loirat, Marie‐Agnès Dragon‐Durey, Wolf H. Fridman, B.J.C. Janssen, Timothy H.J. Goodship, John P. Atkinson

    Wydane 2008
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  20. 20
    Mutation Update of the<i>CLCN5</i>Gene Responsible for Dent Disease 1

    Mutation Update of the<i>CLCN5</i>Gene Responsible for Dent Disease 1 od Lamisse Mansour‐Hendili, Anne Blanchard, Nelly Le Pottier, Isabelle Roncelin, Stéphane Lourdel, Cyrielle Tréard, Wendy González, Ariela Vergara‐Jaque, Gilles Morin, Estelle Colin, Muriel Holder‐Espinasse, Justine Bacchetta, Véronique Baudouin, Stéphane L. Benoit, E. Bérard, Guylhène Bourdat-Michel, Karim Bouchireb, Stéphane Burtey, Mathilde Cailliez, Gérard Cardon, C. Cartery, Gérard Champion, Dominique Chauveau, Pierre Cochat, Karin Dahan, Renaud de la Faille, François-Guillaume Debray, Laurenne Dehoux, Georges Deschênes, Éstelle Desport, Olivier Devuyst, Stella M. Dieguez, Francesco Emma, Michel Fischbach, Denis Fouque, Jacques Fourcade, Arnaud François, Brigitte Gilbert‐Dussardier, Thierry Hannedouche, Pascal Houillier, Hassan Izzedine, Marco Janner, Alexandre Karras, Bertrand Knebelmann, Marie-Pierre Lavocat, Sandrine Lemoine, Valériane Leroy, Chantal Loirat, Marie-Alice Macher, Dominique Martin–Coignard, Denis Morin, Patrick Niaudet, Hubert Nivet, François Nobili, Robert Novo, Laurence Faivre, Claire Rigothier, Gwénaëlle Roussey-Kesler, Rémi Salomon, Andreas Schleich, A.L. Sellier-Leclerc, Kenza Soulami, A. Tiple, Tim Ulinski, Philippe Vanhille, Nicole Van Regemorter, Xavier Jeunemaı̂tre, Rosa Vargas‐Poussou

    Wydane 2015
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