Prenatal bone abnormalities in three cases of familial hypocalciuric hypercalcemia von Frerot, Alice, Baudouin, Véronique, Rideau‐Batista, Aline, Couderc, Anne, Garel, Catherine, Soltane, Samia, Colella, Marina, Vargas‐Poussou, Rosa, Hureaux, Marguerite

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A novel CLCN5 pathogenic mutation supports Dent disease with normal endosomal acidification von Bignon, Yohan, Alekov, Alexi, Frachon, Nadia, Lahuna, Olivier, Jean‐Baptiste Doh‐Egueli, Carine, Deschênes, Georges, Vargas‐Poussou, Rosa, Lourdel, Stéphane

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A mouse model for distal renal tubular acidosis reveals a previously unrecognized role of the V‐ATPase a4 subunit in the proximal tubule von Hennings, J. Christopher, Picard, Nicolas, Huebner, Antje K., Stauber, Tobias, Maier, Hannes, Brown, Dennis, Jentsch, Thomas J., Vargas‐Poussou, Rosa, Eladari, Dominique, Hübner, Christian A.

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Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference von Blanchard, Anne, Bockenhauer, Detlef, Bolignano, Davide, Calò, Lorenzo A., Cosyns, Etienne, Devuyst, Olivier, Ellison, David H., Karet Frankl, Fiona E., Knoers, Nine V.A.M., Konrad, Martin, Lin, Shih-Hua, Vargas-Poussou, Rosa

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Mutations in ATP6V1B1 and ATP6V0A4 genes cause recessive distal renal tubular acidosis in Mexican families von Escobar, Laura I., Simian, Christopher, Treard, Cyrielle, Hayek, Donia, Salvador, Carolina, Guerra, Norma, Matos, Mario, Medeiros, Mara, Enciso, Sandra, Camargo, María Dolores, Vargas‐Poussou, Rosa

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CCDC158: A novel regulator in renal proximal tubular endocytosis unveiled through exome sequencing and interactome analysis von Bondue, Tjessa, Cervellini, Francesca, Smeets, Bart, Strelkov, Sergei V, Horuz-Engels, Flore, Veys, Koenraad, Vargas-Poussou, Rosa, Matteis, Maria Antonietta De, Staiano, Leopoldo, van den Heuvel, Lambertus, Levtchenko, Elena

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Distal renal tubular acidosis: ERKNet/ESPN clinical practice points von Trepiccione, Francesco, Walsh, Steven B, Ariceta, Gema, Boyer, Olivia, Emma, Francesco, Camilla, Roberta, Ferraro, Pietro Manuel, Haffner, Dieter, Konrad, Martin, Levtchenko, Elena, Lopez-Garcia, Sergio Camilo, Santos, Fernando, Stabouli, Stella, Szczepanska, Maria, Tasic, Velibor, Topaloglu, Rezan, Vargas-Poussou, Rosa, Wlodkowski, Tanja, Bockenhauer, Detlef

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Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosis von Louis-Dit-Picard, Helene, Kouranti, Ilektra, Rafael, Chloe, Loisel-Ferreira, Irmine, Chavez-Canales, Maria, Abdel-Khalek, Waed, Argaiz, Eduardo R., Baron, Stephanie, Vacle, Sarah, Migeon, Tiffany, Coleman, Richard, Do Cruzeiro, Marcio, Hureaux, Marguerite, Thurairajasingam, Nirubiah, Decramer, Stephane, Girerd, Xavier, O'Shaugnessy, Kevin, Mulatero, Paolo, Roussey, Gwenaelle, Tack, Ivan, Unwin, Robert, Vargas-Poussou, Rosa, Staub, Olivier, Grimm, Richard, Welling, Paul A., Gamba, Gerardo, Clauser, Eric, Hadchouel, Juliette, Jeunemaitre, Xavier

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Effect of Hydrochlorothiazide on Urinary Calcium Excretion in Dent Disease: An Uncontrolled Trial von Blanchard, Anne, MD, PhD, Vargas-Poussou, Rosa, MD, PhD, Peyrard, Severine, MSc, Mogenet, Agnes, MD, Baudouin, Veronique, MD, PhD, Boudailliez, Bernard, MD, MSc, Charbit, Marina, MD, Deschesnes, George, MD, PhD, Ezzhair, Nadia, MD, Loirat, Chantal, MD, PhD, Macher, Marie-Alice, MD, PhD, Niaudet, Patrick, MD, PhD, Azizi, Michel, MD, PhD

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Relationship between clinical phenotype and in vitro analysis of 13 NPT2c/SCL34A3 mutants von Brazier, François, Courbebaisse, Marie, David, Amandine, Bergerat, David, Leroy, Christine, Lindner, Marta, Maruani, Gérard, Saint Jacques, Camille, Letavernier, Emmanuel, Hureaux, Marguerite, Vargas-Poussou, Rosa, Prié, Dominique

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Observations of a large Dent disease cohort von Blanchard, Anne, Curis, Emmanuel, Guyon-Roger, Tiphaine, Kahila, Diana, Treard, Cyrielle, Baudouin, Véronique, Bérard, Etienne, Champion, Gérard, Cochat, Pierre, Dubourg, Julie, de la Faille, Renaud, Devuyst, Olivier, Deschenes, Georges, Fischbach, Michel, Harambat, Jérôme, Houillier, Pascal, Karras, Alexandre, Knebelmann, Bertrand, Lavocat, Marie-Pierre, Loirat, Chantal, Merieau, Elodie, Niaudet, Patrick, Nobili, François, Novo, Robert, Salomon, Rémi, Ulinski, Tim, Jeunemaître, Xavier, Vargas-Poussou, Rosa

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Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome von Legrand, Anne, Treard, Cyrielle, Roncelin, Isabelle, Dreux, Sophie, Bertholet-Thomas, Aurélia, Broux, Françoise, Bruno, Daniele, Decramer, Stéphane, Deschenes, Georges, Djeddi, Djamal, Guigonis, Vincent, Jay, Nadine, Khalifeh, Tackwa, Llanas, Brigitte, Morin, Denis, Morin, Gilles, Nobili, François, Pietrement, Christine, Ryckewaert, Amélie, Salomon, Rémi, Vrillon, Isabelle, Blanchard, Anne, Vargas-Poussou, Rosa

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

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Claudin‐16 Deficiency Impairs Tight Junction Function in Ameloblasts, Leading to Abnormal Enamel Formation von Bardet, Claire, Courson, Frédéric, Wu, Yong, Khaddam, Mayssam, Salmon, Benjamin, Ribes, Sandy, Thumfart, Julia, Yamaguti, Paulo M, Rochefort, Gael Y, Figueres, Marie‐Lucile, Breiderhoff, Tilman, Garcia‐Castaño, Alejandro, Vallée, Benoit, Le Denmat, Dominique, Baroukh, Brigitte, Guilbert, Thomas, Schmitt, Alain, Massé, Jean‐Marc, Bazin, Dominique, Lorenz, Georg, Morawietz, Maria, Hou, Jianghui, Carvalho‐Lobato, Patricia, Manzanares, Maria Cristina, Fricain, Jean‐Christophe, Talmud, Deborah, Demontis, Renato, Neves, Francisco, Zenaty, Delphine, Berdal, Ariane, Kiesow, Andreas, Petzold, Matthias, Menashi, Suzanne, Linglart, Agnes, Acevedo, Ana Carolina, Vargas‐Poussou, Rosa, Müller, Dominik, Houillier, Pascal, Chaussain, Catherine

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Fetal urine biochemistry in antenatal Bartter syndrome: a case report von Rachid, Myriam L., Dreux, Sophie, Czerkiewicz, Isabelle, Deschênes, Georges, Vargas‐Poussou, Rosa, Mahieu‐Caputo, Dominique, Oury, Jean‐François, Muller, Françoise

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Phenotype–genotype correlation in antenatal and neonatal variants of Bartter syndrome von Brochard, Karine, Boyer, Olivia, Blanchard, Anne, Loirat, Chantal, Niaudet, Patrick, Macher, Marie-Alice, Deschenes, Georges, Bensman, Albert, Decramer, Stéphane, Cochat, Pierre, Morin, Denis, Broux, Françoise, Caillez, Mathilde, Guyot, Claude, Novo, Robert, Jeunemaître, Xavier, Vargas-Poussou, Rosa

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Genetic basis of nephrogenic diabetes insipidus von Hureaux, Marguerite, Vargas-Poussou, Rosa

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Autosomal dominant distal renal tubular acidosis in two pediatric patients with mutations in the SLC4A1 gene. Can the maximum urinary pCO2 test be normal? von Guerra Hernández, Norma E., Gómez Tenorio, Circe, Méndez Silva, Laura Paloma, Moraleda Mesa, Teresa, Escobar, Laura I., Salvador, Carolina, Vargas Poussou, Rosa, García Nieto, Víctor M.

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When a maternal heterozygous mutation of the CYP24A1 gene leads to infantile hypercalcemia through a maternal uniparental disomy of chromosome 20 von Hureaux, Marguerite, Chantot-Bastaraud, Sandra, Cassinari, Kevin, Martinez Casado, Edouard, Cuny, Ariane, Frebourg, Thierry, Vargas-Poussou, Rosa, Brehin, Anne-Claire

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Signification of distal urinary acidification defects in hypocitraturic patients von Forni Ogna, Valentina, Blanchard, Anne, Vargas-Poussou, Rosa, Ogna, Adam, Baron, Stéphanie, Bertocchio, Jean-Philippe, Prot-Bertoye, Caroline, Nevoux, Jérôme, Dubourg, Julie, Maruani, Gérard, Mendes, Margarida, Garcia-Castaño, Alejandro, Treard, Cyrielle, Lepottier, Nelly, Houillier, Pascal, Courbebaisse, Marie

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