Paracellin-1 is critical for magnesium and calcium reabsorption in the human thick ascending limb of Henle von Blanchard, Anne, Jeunemaitre, Xavier, Coudol, Philippe, Dechaux, Michèle, Froissart, Marc, May, Adrien, Demontis, Renato, Fournier, Albert, Paillard, Michel, Houillier, Pascal

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Sildenafil Inhibits Altitude-induced Hypoxemia and Pulmonary Hypertension von Richalet, Jean-Paul, Gratadour, Pierre, Robach, Paul, Pham, Isabelle, Dechaux, Michele, Joncquiert-Latarjet, Aude, Mollard, Pascal, Brugniaux, Julien, Cornolo, Jeremy

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Functional characterization of a calcium-sensing receptor mutation in severe autosomal dominant hypocalcemia with a Bartter-like syndrome von VARGAS-POUSSOU, Rosa, CHUNFA HUANG, HULIN, Philippe, HOUILLIER, Pascal, JEUNEMAITRE, Xavier, PAILLARD, Michel, PLANELLES, Gabrielle, DECHAUX, Michèle, MILLER, R. Tyler, ANTIGNAC, Corinne

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Genetic investigation of autosomal recessive distal renal tubular acidosis : Evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 gene von VARGAS-POUSSOU, Rosa, HOUILLIER, Pascal, ECKART, Philippe, NOVO, Robert, CAILLIEZ, Mathilde, SALOMON, Rémi, NIVET, Hubert, COCHAT, Pierre, TACK, Ivan, FARGEOT, Anne, BOUISSOU, Francois, KESLER, Gwenaelle Roussey, LE POTTIER, Nelly, LOROTTE, Stéphanie, GODEFROID, Nathalie, LAYET, Valérie, MORIN, Gilles, JEUNEMAITRE, Xavier, BLANCHARD, Anne, STROMPF, Laurence, LOIRAT, Chantal, BAUDOUIN, Véronique, MACHER, Marie-Alice, DECHAUX, Michèle, ULINSKI, Tim, NOBILI, Francois

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Transient hyper-17-hydroxyprogesteronemia: a clinical subgroup of patients diagnosed at neonatal screening for congenital adrenal hyperplasia von Cavarzere, Paolo, Samara-Boustani, Dinane, Flechtner, Isabelle, Dechaux, Michèle, Elie, Caroline, Tardy, Véronique, Morel, Yves, Polak, Michel

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Vitamin D Receptor Genotype in Hypophosphatemic Rickets as a Predictor of Growth and Response to Treatment von Jehan, Frédéric, Gaucher, Céline, Nguyen, Thi Minh, Walrant-Debray, Odile, Lahlou, Najiba, Sinding, Christiane, Déchaux, Michèle, Garabédian, Michèle

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Clinical variability of familial tumoral calcinosis caused by novel GALNT3 mutations von Ichikawa, Shoji, Baujat, Geneviève, Seyahi, Aksel, Garoufali, Anastasia G., Imel, Erik A., Padgett, Leah R., Austin, Anthony M., Sorenson, Andrea H., Pejin, Zagorka, Topouchian, Vicken, Quartier, Pierre, Cormier-Daire, Valerie, Dechaux, Michele, Malandrinou, Fotini Ch, Singhellakis, Panagiotis N., Le Merrer, Martine, Econs, Michael J.

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INCREASED β-2 MICROGLOBULINURIA IN HUMAN IMMUNODEFICIENCY VIRUS-1-INFECTED CHILDREN AND ADOLESCENTS TREATED WITH TENOFOVIR von Papaleo, Andrea, Warszawski, Josiane, Salomon, Rémi, Jullien, Vincent, Veber, Florence, Dechaux, Michèle, Blanche, Stéphane

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Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A von Toye, Ashley M., Williamson, Rosalind C., Khanfar, Moudji, Bader-Meunier, Brigitte, Cynober, Thérèse, Thibault, Madeleine, Tchernia, Gil, Déchaux, Michèle, Delaunay, Jean, Bruce, Lesley J.

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Renal function and histology in children after small bowel transplantation von Boyer, Olivia, Noto, Cristian, De Serre, Natacha Patey-Mariaud, Gubler, Marie-Claire, Dechaux, Michèle, Goulet, Olivier, Niaudet, Patrick, Lacaille, Florence

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Chloride Transport in Nasal Ciliated Cells of Cystic Fibrosis Heterozygotes von Sermet-Gaudelus, Isabelle, Dechaux, Michele, Vallee, Benoit, Fajac, Anne, Girodon, Emanuelle, Nguyen-Khoa, Thao, Marianovski, Remi, Hurbain, Ilse, Bresson, Jean Louis, Lenoir, Gerard, Edelman, Aleksander

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Cyclosporin therapy in patients with Alport syndrome von Charbit, Marina, Gubler, Marie-Claire, Dechaux, Michèle, Gagnadoux, Marie-France, Grünfeld, Jean-Pierre, Niaudet, Patrick

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Paracellin-1 is critical for magnesium and calcium reabsorption in the human thick ascending limb of Henle von Blanchard, Anne, Jeunemaitre, Xavier, Coudol, Philippe, Dechaux, Michèle, Froissart, Marc, May, Adrien, Demontis, Renato, Fournier, Albert, Paillard, Michel, Houillier, Pascal

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Primary distal tubular acidosis in childhood: Clinical study and long-term follow-up of 28 patients von Caldas, Alberto, Broyer, Michel, Dechaux, Michèle, Kleinknecht, Claire

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Dietary salt restriction accelerates atherosclerosis in apolipoprotein E-deficient mice von Ivanovski, Ognen, Szumilak, Dorota, Nguyen-Khoa, Thao, Dechaux, Michele, Massy, Ziad A., Phan, Olivier, Mothu, Nadya, Lacour, Bernard, Drueke, Tilman B., Muntzel, Martin

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Improvement of renal function in pediatric heart transplant recipients treated with low-dose calcineurin inhibitor and mycophenolate mofetil von BOYER, Olivia, LE BIDOIS, Jérome, DECHAUX, Michèle, GUBLER, Marie-Claire, NIAUDET, Patrick

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Band 3 Courcouronne: Homozygous Mutation Ser667Phe Causes Severe Hereditary Spherocytosis and Incomplete Distal Renal Tubular Acidosis von Delaunay, Jean, Toye, Ashley, Williamson, Rosalind, Khanfar, Moudji, Bader-Meunier, Brigitte, Cynober, Thérèse, Thibault, Madeleine, Tchernia, Gilbert Jean, Déchaux, Michèle, Bruce, Lesley

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Basic protocol for transepithelial nasal potential difference measurements von Schüler, Daniel, Sermet-Gaudelus, Isabelle, Wilschanski, Michael, Ballmann, Manfred, Dechaux, Michèle, Edelman, Aleksander, Hug, Martin, Leal, Teresinha, Lebacq, Jean, Lebecque, Patrick, Lenoir, Gérard, Stanke, Frauke, Wallemacq, Pierre, Tümmler, Burkhard, Knowles, Michael R.

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Functional studies of twelve mutant V2 vasopressin receptors related to nephrogenic diabetes insipidus : Molecular basis of a mild clinical phenotype von ALA, Y, MORIN, D, TURNER, M. S, BALESTRE, M.-N, ALONSO, G, HIBERT, M, BARBERIS, C, HENDY, G. N, BICHET, D. G, JARD, S, MOUILLAC, B, SABATIER, N, VARGAS, R, COTTE, N, DECHAUX, M, ANTIGNAC, C, ARTHUS, M.-F, LONERGAN, M

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Vasopressin increases glomerular filtration rate in conscious rats through its antidiuretic action von Bouby, N, Ahloulay, M, Nsegbe, E, Déchaux, M, Schmitt, F, Bankir, L

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