Результаты поиска - G. Roussey

  • Отображение 1 - 12 результаты of 12
Отмена результатов
  1. 1
    Treatment by immunoadsorption for recurrent focal segmental glomerulosclerosis after paediatric kidney transplantation: a multicentre French cohort

    Treatment by immunoadsorption for recurrent focal segmental glomerulosclerosis after paediatric kidney transplantation: a multicentre French cohort по Lise Allard, Thérèsa Kwon, Saoussen Krid, Justine Bacchetta, Arnaud Garnier, Robert Novo, Georges Deschênes, Rémi Salomon, G. Roussey, Emma Allain‐Launay

    Опубликовано 2017
    Полный текст Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  2. 2
    Uropathogen Resistance and Antibiotic Prophylaxis: A Meta-analysis

    Uropathogen Resistance and Antibiotic Prophylaxis: A Meta-analysis по Rachel E. Selekman, Daniel J. Shapiro, John Boscardin, Gabrielle Williams, Jonathan C. Craig, Per Brandström, Marco Pennesi, G. Roussey-Kesler, Pankaj Hari, Hillary L. Copp

    Опубликовано 2018
    Полный текст Полный текст
    Revisão
    Добавить в Избранное
    Сохранить в:
  3. 3
    Fatal thrombotic microangiopathy case following adeno-associated viral <i>SMN</i> gene therapy

    Fatal thrombotic microangiopathy case following adeno-associated viral <i>SMN</i> gene therapy по Julia Guillou, Alice de Pellegars, Florence Porcheret, Véronique Frémeaux‐Bacchi, Emma Allain‐Launay, Camille Debord, M. Denis, Yann Péréon, Christine Barnérias, Isabelle Desguerre, G. Roussey, Sandra Mercier

    Опубликовано 2022
    Полный текст Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  4. 4
    Quality of life in adolescents with chronic kidney disease who initiate haemodialysis treatment

    Quality of life in adolescents with chronic kidney disease who initiate haemodialysis treatment по Stéphanie Clavé, Michel Tsimaratos, Mohamed Boucékine, Bruno Ranchin, Rémi Salomon, Olivier Dunand, Arnaud Garnier, Annie Lahoche, Marc Fila, G. Roussey, Françoise Broux, Jérôme Harambat, Sylvie Cloarec, Soraya Menouer, Georges Deschênes, Isabelle Vrillon, Pascal Auquier, Julie Berbis

    Опубликовано 2019
    Полный текст Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  5. 5
    Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment

    Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment по Patricie Burda, Alice Küster, Ola Hjalmarson, Terttu Suormala, Céline Bürer, Seraina Lutz, G. Roussey, Laurence Christa, Jorge Asin-Cayuela, Gittan Kollberg, Bengt Åndersson, David Watkins, David S. Rosenblatt, Brian Fowler, E Holme, D. Sean Froese, Matthias R. Baumgartner

    Опубликовано 2015
    Полный текст
    Revisão
    Добавить в Избранное
    Сохранить в:
  6. 6
    Complement Gene Variants and Shiga Toxin–Producing Escherichia coli–Associated Hemolytic Uremic Syndrome

    Complement Gene Variants and Shiga Toxin–Producing Escherichia coli–Associated Hemolytic Uremic Syndrome по Véronique Frémeaux‐Bacchi, Anne‐Laure Sellier‐Leclerc, Paula Vieira‐Martins, Sophie Limou, Thérèsa Kwon, Annie Lahoche, Robert Novo, Brigitte Llanas, François Nobili, G. Roussey, Mathilde Cailliez, Tim Ulinski, Georges Deschênes, Corinne Alberti, François‐Xavier Weill, Patricia Mariani, Chantal Loirat

    Опубликовано 2019
    Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  7. 7
    Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children

    Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children по Mathilde Glénisson, Mathilde Grapin, Thomas Blanc, Evgenia Preka, Julien Hogan, Manon Aurelle, G. Roussey, Antoine Mouche, Caroline Rousset‐Rouvière, Robert Novo, Camille Faudeux, Marc Fila, Isabelle Vrillon, Sylvie Cloarec, Tabassome Simon, Jérôme Harambat, Edouard Martinez Casado, Julien Rod, Morgane Carre Lecoindre, Laurence Heidet, Olivia Boyer, Nicolas Garcelon, Jessica Kachmar, Guillaume Dorval, Sabine Sarnacki

    Опубликовано 2025
    Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  8. 8
    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 по 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

    Опубликовано 2015
    Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  9. 9
    Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosis

    Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosis по 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

    Опубликовано 2020
    Полный текст Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  10. 10
    Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations

    Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations по Graciana Jaureguiberry, Muriel De La Dure‐Molla, David Parry, Mickaël Quentric, Nina Himmerkus, Toshiyasu Koike, James A. Poulter, Enriko Klootwijk, Steven L. Robinette, Alexander J. Howie, Vaksha Patel, Marie-Lucile Figueres, Horia Stanescu, Naomi Issler, Jeremy K. Nicholson, Detlef Böckenhauer, Christopher Laing, Stephen B. Walsh, David A. McCredie, Sue Povey, Audrey Asselin, Arnaud Picard, Aurore Coulomb, Alan Medlar, Isabelle Bailleul‐Forestier, Alain Verloès, Cédric Le Caignec, G. Roussey, J. Guiol, Bertrand Isidor, Clare V. Logan, Richard F. Shore, Colin A. Johnson, C.F. Inglehearn, Suhaila Al‐Bahlani, Matthieu Schmittbuhl, François Clauss, Mathilde Huckert, Virginie Laugel, Emmanuelle Ginglinger, Sandra Pajarola, Giuseppina Spartà, Deborah Bartholdi, Anita Rauch, Marie-Claude Addor, Paulo Márcio Yamaguti, H.P.N. Safatle, Ana Carolina Acevedo, Hercílio Martelli‐Júnior, Pedro E. dos Santos Netos, Ricardo D. Coletta, Sandra Gruessel, Carolin Sandmann, Denise Ruehmann, Craig B. Langman, Steven J. Scheinman, Didem Özdemır, Thomas C. Hart, P. Suzanne Hart, Ute Neugebauer, Eberhard Schlatter, Pascal Houillier, William A. Gahl, Miikka Vikkula, Agnès Bloch‐Zupan, Markus Bleich, Hiroshi Kitagawa, Robert J. Unwin, Alan J. Mighell, Ariane Berdal, Robert Kleta

    Опубликовано 2013
    Полный текст Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  11. 11
    Global Variation of Nutritional Status in Children Undergoing Chronic Peritoneal Dialysis: A Longitudinal Study of the International Pediatric Peritoneal Dialysis Network

    Global Variation of Nutritional Status in Children Undergoing Chronic Peritoneal Dialysis: A Longitudinal Study of the International Pediatric Peritoneal Dialysis Network по Franz Schaefer, Laura Benner, Dagmara Borzych–Dużałka, Joshua J. Zaritsky, Hong Xu, Lesley Rees, Zenaida L. Antonio, Erkin Serdaroğlu, Nakysa Hooman, Hiren P. Patel, Lale Sever, Karel Vondrák, Joseph T. Flynn, Anabella Rébori, William Wong, Tuula Hölttä, Zeynep Yürük Yıldırım, Bruno Ranchin, Ryszard Grenda, Sara Testa, Dorota Drożdż, Attila J. Szabó, Loai Eid, Biswanath Basu, Renata Vitkevič, Cynthia Wong, Stephen J. Pottoore, Dominik N. Müller, Ruhan Düşünsel, Claudia González, Marc Fila, Lisa Sartz, Anja Sander, Bradley A. Warady, M Adragna, Paula A. Coccia, Ángela Suárez, Patricia G. Vallés, Reza Salim, Laura Alconcher, Klaus Arbeiter, K. van Hoeck, Vera Hermina Kalika Koch, Janusz Feber, Elizabeth Harvey, Colin White, M. Valenzuela, Jorge Villagrá, F. Cano, M Contreras, A. Vogel, Pedro Sepúlveda Zambrano, P Hevia, Mc Chiu, Jie Ding, Juan José Vanegas, Lina María Serna‐Higuita, G. Roussey, Tim Ulinski, Saoussen Krid, Michel Fischbach, Jérôme Harambat, Ch. Samaille, Rainer Büscher, Jun Oh, Lars Pape, Ulrich John, Günter Klaus, H. Billing, C. Stafanidis, Fotiοs Papachristou, Arvind Bagga, Madhuri Kanitkar, Rajiv Sinha, Sanjum S. Sethi, Enrico Verrina, Enrico Vidal, Giovanna Leozappa, Daniel Landau, Il Soo Ha, Kyu-hyun Paik, Ahmad Bilal, E Sahpazova, Yam-Ngo Lim, Lorena Sànchez Barbosa, Jaap W. Groothoff, Y. Konijenberg, Yolanda Silva, M. Al Ryami, Reyner Loza Munárriz, Bożena Leszczyńska, Maria Szczepańska, O Brumariu, Jameela A. Kari, D Kruscić, Hui‐Kim Yap, Gema Ariceta, Mireia Aguirre, Fernando Santos, Bogna Niwinska-Faryna

    Опубликовано 2019
    Полный текст Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:
  12. 12
    The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies

    The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies по 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

    Опубликовано 2023
    Полный текст
    Artigo
    Добавить в Избранное
    Сохранить в:

Инструменты поиска: