检索结果 - Marie‐Alice Macher

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  1. 1
    Rituximab in steroid-dependent idiopathic nephrotic syndrome in childhood--follow-up after CD19 recovery

    Rituximab in steroid-dependent idiopathic nephrotic syndrome in childhood--follow-up after CD19 recovery 由 A.-L. Sellier-Leclerc, Véronique Baudouin, Thérèsa Kwon, Marie‐Alice Macher, Valérie Guérin, Hélène Lapillonne, Georges Deschênes, Tim Ulinski

    出版 2011
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  2. 2
    Successful pre-transplant management of a patient with anti-factor H autoantibodies-associated haemolytic uraemic syndrome

    Successful pre-transplant management of a patient with anti-factor H autoantibodies-associated haemolytic uraemic syndrome 由 Thérèsa Kwon, Marie‐Agnès Dragon‐Durey, Marie‐Alice Macher, Véronique Baudouin, Anne Maisin, Michel Peuchmaur, Véronique Frémeaux‐Bacchi, Chantal Loirat

    出版 2008
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  3. 3
    Benefits of kidney transplantation for a national cohort of patients aged 70 years and older starting renal replacement therapy

    Benefits of kidney transplantation for a national cohort of patients aged 70 years and older starting renal replacement therapy 由 Camille Legeai, Roland Andrianasolo, Olivier Moranne, Renaud Snanoudj, Maryvonne Hourmant, Marc Bauwens, Joaquim Soares, Christian Jacquelinet, Cécile Couchoud, Marie‐Alice Macher

    出版 2018
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  4. 4
    Anti–Factor H Autoantibodies Associated with Atypical Hemolytic Uremic Syndrome

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

    出版 2004
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  5. 5
    Drug administration errors and their determinants in pediatric in-patients

    Drug administration errors and their determinants in pediatric in-patients 由 Sonia Prot, Jean Fontan, Corinne Alberti, Olivier Bourdon, Caroline Farnoux, Marie Alice Macher, Anita Foureau, Albert Faye, François Beaufils, Serge Gottot, Françoise Brion

    出版 2005
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  6. 6
    Individual and Regional Factors of Access to the Renal Transplant Waiting List in France in a Cohort of Dialyzed Patients

    Individual and Regional Factors of Access to the Renal Transplant Waiting List in France in a Cohort of Dialyzed Patients 由 Sahar Bayat, Marie‐Alice Macher, Cécile Couchoud, Florian Bayer, Mathilde Lassalle, Emmanuel Villar, Yvanie Caillé, Sylvie Mercier, V. Joyeux, C. Noël, M. Kessler, Christian Jacquelinet

    出版 2015
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  7. 7
    A Humanized Mouse Model of Idiopathic Nephrotic Syndrome Suggests a Pathogenic Role for Immature Cells

    A Humanized Mouse Model of Idiopathic Nephrotic Syndrome Suggests a Pathogenic Role for Immature Cells 由 Anne‐Laure Sellier‐Leclerc, Arnaud Duval, SteCombining Acute Accentphanie Riveron, Marie-Alice Macher, Georges Deschênes, Chantal Loirat, Marie‐Christine Verpont, Michel Peuchmaur, Pierre Ronco, Renato C. Monteiro, Élie Haddad

    出版 2007
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  8. 8
    Improving Mutation Screening in Familial Hematuric Nephropathies through Next Generation Sequencing

    Improving Mutation Screening in Familial Hematuric Nephropathies through Next Generation Sequencing 由 Vincent Morinière, Karin Dahan, Pascale Hilbert, Marieline Lison, Saïd Lebbah, Alexandra Topa, Christine Bôle‐Feysot, Solenn Pruvost, Patrick Nitschké, Emmanuelle Plaisier, Bertrand Knebelmann, Marie‐Alice Macher, Laure‐Hélène Noël, Marie‐Claire Gubler, Corinne Antignac, Laurence Heidet

    出版 2014
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  9. 9
    Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies

    Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies 由 Aude Servais, Laure‐Hélène Noël, Lubka T. Roumenina, Moglie Le Quintrec, Stéphanie Ngo, Marie‐Agnès Dragon‐Durey, Marie-Alice Macher, Julien Zuber, Alexandre Karras, François Provôt, Bruno Moulin, Jean‐Pierre Grünfeld, Patrick Niaudet, Philippe Lesavre, Véronique Frémeaux‐Bacchi

    出版 2012
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  10. 10
    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 由 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

    出版 2009
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  11. 11
    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 由 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

    出版 2009
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  12. 12
    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 由 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

    出版 2007
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  13. 13
    Mutational analysis of the PLCE1 gene in steroid resistant nephrotic syndrome

    Mutational analysis of the PLCE1 gene in steroid resistant nephrotic syndrome 由 Olivia Boyer, Geneviève Benoît, Olivier Gribouval, Fabien Névo, Audrey Pawtowski, İlmay Bilge, Zelâl Bircan, Georges Deschênes, Lisa M. Guay‐Woodford, Michelle Hall, Marie Alice Macher, Kenza Soulami, Constantinos J. Stefanidis, Robert B. Weiss, Chantal Loirat, Marie‐Claire Gubler, Corinne Antignac

    出版 2010
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  14. 14
    Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome

    Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome 由 Lubka T. Roumenina, Mathieu Jablonski, Christophe Hue, Jacques Blouin, Jordan D. Dimitrov, Marie‐Agnès Dragon‐Durey, Mathieu Cayla, Wolf H. Fridman, Marie-Alice Macher, David Ribes, L Moulonguet, Lionel Rostaing, Simon C. Satchell, Peter W. Mathieson, Catherine Sautès‐Fridman, Chantal Loirat, Catherine H. Régnier, Lise Halbwachs‐Mecarelli, Véronique Frémeaux‐Bacchi

    出版 2009
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  15. 15
    Building Kidney Exchange Programmes in Europe—An Overview of Exchange Practice and Activities

    Building Kidney Exchange Programmes in Europe—An Overview of Exchange Practice and Activities 由 Péter Bíró, Bernadette Haase‐Kromwijk, Tommy Andersson, Eyjólfur Ingi Ásgeirsson, Tatiana Baltesová, Ioannis Boletis, Catarina Bolotinha, Gregor Bond, Georg A. Böhmig, Lisa Burnapp, Katarı́na Cechlárová, Paola Di Ciaccio, Jiří Froněk, Karine Hadaya, Aline C. Hemke, Christian Jacquelinet, Rachel Johnson, R. Kieszek, Dirk Kuypers, R. Leishman, Marie‐Alice Macher, David F. Manlove, Georgia Menoudakou, Mikko Salonen, Bart Smeulders, Vito Sparacino, Frits Spieksma, María O. Valentín, Nic Wilson, Joris van der Klundert

    出版 2018
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  16. 16
    Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences

    Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences 由 Rosa Vargas‐Poussou, Lamisse Mansour‐Hendili, Stéphanie Baron, Jean‐Philippe Bertocchio, C. Travers, Christophe Simian, Cyrielle Tréard, Véronique Baudouin, Sonia Beltran, Françoise Broux, Odile Camard, Sylvie Cloarec, Catherine Cormier, Xavier Debussche, Emmanuelle Dubosclard, Celine Eid, Jean‐Philippe Haymann, Soto Romuald Kiando, Jean‐Marc Kuhn, Guy Lefort, Agnès Linglart, Bernadette Lucas-Pouliquen, Marie‐Alice Macher, Gérard Maruani, Sophie Ouzounian, Michel Polak, E Requeda, Dominique Robier, Caroline Silve, Jean‐Claude Souberbielle, Ivan Tack, Delphine Vezzosi, Xavier Jeunemaı̂tre, Pascal Houillier

    出版 2016
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  17. 17
    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 由 Christelle Arrondel, Sophia Missoury, Rozemarijn Snoek, Julie Patat, Giulia Menara, Bruno Collinet, Dominique Liger, D. Durand, Olivier Gribouval, Olivia Boyer, Laurine Buscara, Gaëlle Martin, Eduardo Machuca, Fabien Névo, 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

    出版 2019
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  18. 18
    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 由 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

    出版 2015
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  19. 19
    The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies

    The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies 由 Friederike Petzold, Katy Billot, Xiaoyi Chen, C. Henry, Emilie Filhol, Yoann Martin, Marina Avramescu, Maxime Douillet, Vincent Morinière, Pauline Krug, Marc Jeanpierre, Kálmán Tory, Olivia Boyer, Anita Burgun, Aude Servais, Rémi Salomon, Alexandre Benmerah, Laurence Heidet, Nicolas Garcelon, Corinne Antignac, Mohamad Zaidan, Sophie Saunier, Tania Attié‐Bitach, Valerie Comier-Daire, Jean‐Michel Rozet, Yaacov Frishberg, Brigitte Llanas, M. Broyer, Nabil Mohsin, Marie‐Alice Macher, Nicole Philip, Véronique Baudouin, D. Brackman, Chantal Loirat, Marina Charbit, Maud Dehennault, C. Guyot, Pierre Bataille, Mariet Elting, Georges Deschênes, Andrea Gropman, Geneviève Guest, Marie‐France Gagnadoux, Philippe Nicoud, Pierre Cochat, Bruno Ranchin, A Bensman, Anne‐Marie Guerrot, Bertrand Knebelmann, İlmay Bilge, Bruno Daniele, Stéphane Burtey, Caroline Rousset Rouvière, Valérie Caudwell, Denis Morin, Hélène Dollfus, Anne Maisin, Christian Hamel, Éric Bieth, Sophie Gié, Judith Goodship, G. Roussey, Hermine La Selve, Hubert Nivet, Lucie Bessenay, Mathilde Caillez, Jean Bernard Palcoux, Stéphane L. Benoit, Philippe Dubot, Marc Fila, Fabienne Giuliano, Daouya Iftene, M. Kessler, Thérèsa Kwon, A. Lahoche, Audrey Laurent, Anne-Laure Leclerc, David V. Milford, Thomas J. Neuhaus, Sylvie Odent, Philippe Eckart, Dominique Chauveau, Patrick Niaudet, Horacio A. Repetto, Sophie Taque, Alexandra Bruel, Alexandra Noel-Botte, Emma Allain Launay, Lisa Allard, Dany Anlicheau, Anne-Laure Adra, Arnaud Garnier, Arvind Nagra, Remy Baatard, Justine Bacchetta, Banu Sadıkoğlu, Christine Barnérias, Anne Barthélémy, Lina Basel, Nader Bassilios

    出版 2023
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