Søgeresultater - Isabelle Vrillon
- Showing 1 - 4 results of 4
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1
Quality of life in adolescents with chronic kidney disease who initiate haemodialysis treatment af 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
Udgivet 2019Artigo -
2
Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome af 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
Udgivet 2017Artigo -
3
Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children af 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
Udgivet 2025Artigo -
4
Clinical and Genetic Spectrum of Bartter Syndrome Type 3 af 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
Udgivet 2017Artigo
Søgeredskaber:
Relaterede emner
Medicine
Biology
Gene
Genetics
Bartter syndrome
Environmental health
Frameshift mutation
Hypokalemia
Internal medicine
Missense mutation
Mutation
Population
Chemistry
Clinical psychology
Cohort
Coping (psychology)
Endocrinology
Gene mutation
Genotype
Genotype-phenotype distinction
Gerontology
Gitelman syndrome
Hypomagnesemia
Magnesium
Nonsense mutation
Nursing
Obstetrics
Organic chemistry
Pediatrics
Phenotype