Kidney Function and Influence of Sunlight Exposure in Patients With Impaired 24-Hydroxylation of Vitamin D Due to CYP24A1 Mutations von Figueres, Marie-Lucile, MD, Linglart, Agnès, MD, PhD, Bienaime, Frank, MD, PhD, Allain-Launay, Emma, MD, Roussey-Kessler, Gwenaelle, MD, Ryckewaert, Amélie, MD, Kottler, Marie-Laure, MD, PhD, Hourmant, Maryvonne, MD, PhD

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Characterization of Renal Injury and Inflammation in an Experimental Model of Intravascular Hemolysis von Merle, Nicolas S, Grunenwald, Anne, Figueres, Marie-Lucile, Chauvet, Sophie, Daugan, Marie, Knockaert, Samantha, Robe-Rybkine, Tania, Noe, Remi, May, Olivia, Frimat, Marie, Brinkman, Nathan, Gentinetta, Thomas, Miescher, Sylvia, Houillier, Pascal, Legros, Veronique, Gonnet, Florence, Blanc-Brude, Olivier P, Rabant, Marion, Daniel, Regis, Dimitrov, Jordan D, Roumenina, Lubka T

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Crystalline light chain proximal tubulopathy with chronic renal failure and silicone gel breast implants: 1 case report von Figueres, Marie-Lucile, MD, Beaume, Julie, MD, Vuiblet, Vincent, MD, Rabant, Marion, MD, Bassilios, Nader, MD, Herody, Michel, MD, Touchard, Guy, MD, PhD, Noël, Laure-Hélène, MD

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Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome von Hadj-Rabia, Smail, Brideau, Gaelle, Al-Sarraj, Yasser, Maroun, Rachid C, Figueres, Marie-Lucile, Leclerc-Mercier, Stéphanie, Olinger, Eric, Baron, Stéphanie, Chaussain, Catherine, Nochy, Dominique, Taha, Rowaida Z, Knebelmann, Bertrand, Joshi, Vandana, Curmi, Patrick A, Kambouris, Marios, Vargas-Poussou, Rosa, Bodemer, Christine, Devuyst, Olivier, Houillier, Pascal, El-Shanti, Hatem

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Heterogeneous histologic and clinical evolution in 3 cases of dense deposit disease with long-term follow-up von Figuères, Marie-Lucile, Frémeaux-Bacchi, Véronique, Rabant, Marion, Galmiche, Louise, Marinozzi, Maria Chiara, Grünfeld, Jean-Pierre, Noël, Laure-Hélène, Servais, Aude

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

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Intravascular hemolysis induces complement system activation von Merle, Nicolas S., Grunenwald, Anne, Rajaratnam, Helena, Gnemmi, Viviane, Frimat, Marie, Figueres, Marie-Lucile, Bouzekri, Sanah, Charue, Dominique, Noe, Remi, Robe-Rybkine, Tania, Brinkman, Nathan, Miescher, Sylvia, Le Jeune, Sylvain, Houillier, Pascal, Dimitrov, Jordan D., Fremeaux-Bacchi, Veronique, Blanc-Brude, Olivier P., Roumenina, Lubka. T.

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Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations von JAUREGUIBERRY, Graciana, DE LA DURE-MOLLA, Muriel, PATEL, Vaksha, FIGUERES, Marie-Lucile, STANESCU, Horia C, ISSLER, Naomi, NICHOLSON, Jeremy K, BOCKENHAUER, Detlef, LAING, Christopher, WALSH, Stephen B, MCCREDIE, David A, POVEY, Sue, PARRY, David, ASSELIN, Audrey, PICARD, Arnaud, COULOMB, Aurore, MEDLAR, Alan J, BAILLEUL-FORESTIER, Isabelle, VERLOES, Alain, LE CAIGNEC, Cedric, ROUSSEY, Gwenaelle, GUIOL, Julien, ISIDOR, Bertrand, QUENTRIC, Mickael, LOGAN, Clare, SHORE, Roger, JOHNSON, Colin, INGLEHEARN, Christopher, AL-BAHLANI, Suhaila, SCHMITTBUHL, Matthieu, CLAUSS, François, HUCKERT, Mathilde, LAUGEL, Virginie, GINGLINGER, Emmanuelle, HIMMERKUS, Nina, PAJAROLA, Sandra, SPARTA, Giuseppina, BARTHOLDI, Deborah, RAUCH, Anita, ADDOR, Marie-Claude, YAMAGUTI, Paulo M, SAFATLE, Heloisa P, ACEVEDO, Ana Carolina, MARTELLI-JUNIOR, Hercílio, DOS SANTOS NETOS, Pedro E, KOIKE, Toshiyasu, COLETTA, Ricardo D, GRUESSEL, Sandra, SANDMANN, Carolin, RUEHMANN, Denise, LANGMAN, Craig B, SCHEINMAN, Steven J, OZDEMIR-OZENEN, Didem, HART, Thomas C, SUZANNE HART, P, NEUGEBAUER, Ute, POULTER, James, KLOOTWIJK, Enriko, ROBINETTE, Steven L, HOWIE, Alexander J

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Aspergillus arthritis and organ transplantation von Figuères, Marie-Lucile, Cantarovich, Diego, Tattevin, Pierre, Le Pogamp, Patrick, Polard, Jean-Louis, Stock, Nathalie, Blancho, Gilles

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