Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification

Por de La Dure-Molla, Muriel, Philippe Fournier, Benjamin, Berdal, Ariane
Publicado no Eur J Hum Genet (2015)

MSX2 in ameloblast cell fate and activity

Por Babajko, Sylvie, de La Dure-Molla, Muriel, Jedeon, Katia, Berdal, Ariane
Publicado no Front Physiol (2015)

FAM20A Gene Mutation: Amelogenesis or Ectopic Mineralization?

Por Lignon, Guilhem, Beres, Fleur, Quentric, Mickael, Rouzière, Stephan, Weil, Raphael, De La Dure-Molla, Muriel, Naveau, Adrien, Kozyraki, Renata, Dessombz, Arnaud, Berdal, Ariane
Publicado no Front Physiol (2017)

Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations

Por de la Dure-Molla, Muriel, Quentric, Mickael, Yamaguti, Paulo Marcio, Acevedo, Ana-Carolina, Mighell, Alan J, Vikkula, Miikka, Huckert, Mathilde, Berdal, Ariane, Bloch-Zupan, Agnes
Publicado em 2014

Management of rare diseases of the Head, Neck and Teeth: results of a French population-based prospective 8-year study

Por Friedlander, Lisa, Choquet, Rémy, Galliani, Eva, de Chalendar, Myriam, Messiaen, Claude, Ruel, Amélie, Vazquez, Marie-Paule, Berdal, Ariane, Alberti, Corinne, De La Dure Molla, Muriel
Publicado no Orphanet J Rare Dis (2017)

Tracking Endogenous Amelogenin and Ameloblastin In Vivo

Por Jacques, Jaime, Hotton, Dominique, De la Dure-Molla, Muriel, Petit, Stephane, Asselin, Audrey, Kulkarni, Ashok B., Gibson, Carolyn Winters, Brookes, Steven Joseph, Berdal, Ariane, Isaac, Juliane
Publicado em 2014

Enamel Defects Reflect Perinatal Exposure to Bisphenol A

Por Jedeon, Katia, De la Dure-Molla, Muriel, Brookes, Steven J., Loiodice, Sophia, Marciano, Clémence, Kirkham, Jennifer, Canivenc-Lavier, Marie-Chantal, Boudalia, Sofiane, Bergès, Raymond, Harada, Hidemitsu, Berdal, Ariane, Babajko, Sylvie
Publicado em 2013

A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement

Por Prasad, Megana K, Geoffroy, Véronique, Vicaire, Serge, Jost, Bernard, Dumas, Michael, Le Gras, Stéphanie, Switala, Marzena, Gasse, Barbara, Laugel-Haushalter, Virginie, Paschaki, Marie, Leheup, Bruno, Droz, Dominique, Dalstein, Amelie, Loing, Adeline, Grollemund, Bruno, Muller-Bolla, Michèle, Lopez-Cazaux, Séréna, Minoux, Maryline, Jung, Sophie, Obry, Frédéric, Vogt, Vincent, Davideau, Jean-Luc, Davit-Beal, Tiphaine, Kaiser, Anne-Sophie, Moog, Ute, Richard, Béatrice, Morrier, Jean-Jacques, Duprez, Jean-Pierre, Odent, Sylvie, Bailleul-Forestier, Isabelle, Rousset, Monique Marie, Merametdijan, Laure, Toutain, Annick, Joseph, Clara, Giuliano, Fabienne, Dahlet, Jean-Christophe, Courval, Aymeric, El Alloussi, Mustapha, Laouina, Samir, Soskin, Sylvie, Guffon, Nathalie, Dieux, Anne, Doray, Bérénice, Feierabend, Stephanie, Ginglinger, Emmanuelle, Fournier, Benjamin, de la Dure Molla, Muriel, Alembik, Yves, Tardieu, Corinne, Clauss, François, Berdal, Ariane, Stoetzel, Corinne, Manière, Marie Cécile, Dollfus, Hélène, Bloch-Zupan, Agnès
Publicado no J Med Genet (2016)

Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations

Por 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
Publicado em 2013