Որոնման արդյունքները - Mathilde Cailliez
- Ցուցադրվում են 1 - 5 արդյունքները 5
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1
Pathogenic Variants in Complement Genes and Risk of Atypical Hemolytic Uremic Syndrome Relapse after Eculizumab Discontinuation Fádi Fakhouri, Marc Fila, François Provôt, Yahsou Delmas, Christelle Barbet, Valérie Châtelet, Cédric Rafat, Mathilde Cailliez, Julien Hogan, Aude Servais, Alexandre Karras, Raïfah Makdassi, Feriell Louillet, Jean‐Philippe Coindre, Éric Rondeau, Chantal Loirat, Véronique Frémeaux‐Bacchi
Հրապարակվել է 2016Artigo -
2
C5 nephritic factors drive the biological phenotype of C3 glomerulopathies Maria-Chiara Marinozzi, Sophie Chauvet, Moglie Le Quintrec, Morgane Mignotet, Florent Petitprez, Christophe Legendre, Mathilde Cailliez, Georges Deschênes, Michel Fischbach, Alexandre Karras, François Nobili, Christine Piétrement, Marie‐Agnès Dragon‐Durey, Fádi Fakhouri, Lubka T. Roumenina, Véronique Frémeaux‐Bacchi
Հրապարակվել է 2017Artigo -
3
Complement Gene Variants and Shiga Toxin–Producing Escherichia coli–Associated Hemolytic Uremic Syndrome 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
Հրապարակվել է 2019Artigo -
4
Clinical and Genetic Spectrum of Bartter Syndrome Type 3 Elsa Seys, Olga Andrini, Mathilde Keck, Lamisse Mansour‐Hendili, Pierre‐Yves Courand, Christophe Simian, Georges Deschênes, Thérèsa Kwon, Aurélia Bertholet‐Thomas, Guillaume Bobrie, Jean Sébastien Borde, Guylhène Bourdat-Michel, Stéphane Decramer, Mathilde Cailliez, Pauline Krug, P Cozette, Jean‐Daniel Delbet, Laurence Dubourg, Dominique Chaveau, Marc Fila, Noémie Jourde‐Chiche, Bertrand Knebelmann, Marie‐Pierre Lavocat, Sandrine Lemoine, D. Djeddi, Brigitte Llanas, Férielle Louillet, Élodie Merieau, Maria Mileva, Luísa Mota‐Vieira, Christiane Mousson, François Nobili, Robert Novo, Gwénaëlle Roussey-Kesler, Isabelle Vrillon, Stephen B. Walsh, Jacques Teulon, Anne Blanchard, Rosa Vargas‐Poussou
Հրապարակվել է 2017Artigo -
5
Mutation Update of the<i>CLCN5</i>Gene Responsible for Dent Disease 1 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
Հրապարակվել է 2015Revisão
Որոնման գործիքներ:
Առնչվող խորագիր
Internal medicine
Medicine
Biology
Gene
Genetics
Antibody
Atypical hemolytic uremic syndrome
Complement system
Dialysis
Endocrinology
Immunology
Kidney
Missense mutation
Phenotype
Alternative complement pathway
Bartter syndrome
CD46
Chemistry
Discontinuation
Disease
Eculizumab
Escherichia coli
Frameshift mutation
Gastroenterology
Genotype
Gitelman syndrome
Glomerulonephritis
Hypercalciuria
Hypokalemia
Hypomagnesemia