MSX2 in ameloblast cell fate and activity

por Babajko, Sylvie, de La Dure-Molla, Muriel, Jedeon, Katia, Berdal, Ariane
Publicado 2015

Gingival inflammation, enamel defects, and tooth sensitivity in children with amelogenesis imperfecta: a case-control study

por QUANDALLE, Camille, BOILLOT, Adrien, FOURNIER, Benjamin, GARREC, Pascal, DE LA DURE-MOLLA, Muriel, Stephane, KERNER
Publicado 2020

Oral lesions of viral, bacterial, and fungal diseases in children: A decision tree

por Guillouet, Charlotte, Riou, Margot C., Duong, Lucas T., de La Dure-Molla, Muriel, Fournier, Benjamin P. J.
Publicado 2022

Amelogenesis imperfecta: therapeutic strategy from primary to permanent dentition across case reports

por Toupenay, Steve, Fournier, Benjamin Philippe, Manière, Marie-Cécile, Ifi-Naulin, Chantal, Berdal, Ariane, de La Dure– Molla, Muriel
Publicado 2018

Translation and validation of the French version of the Child Perceptions Questionnaire for children aged from 8 to 10 years old (CPQ (8-10))

por Boy-Lefèvre, Marie-Laure, Razanamihaja, Noéline, Azogui-Lévy, Sylvie, Vigneron, Andréa, Jordan, Laurence, Berdal, Ariane, de la Dure-Molla, Muriel
Publicado 2018

Parental–Caregivers Perceptions Questionnaire (P-CPQ): translation and evaluation of psychometric properties of the French version of the questionnaire

por Razanamihaja, Noeline, Boy-Lefèvre, Marie-Laure, Jordan, Laurence, Tapiro, Lea, Berdal, Ariane, de la Dure-Molla, Muriel, Azogui-Levy, Sylvie
Publicado 2018

The dental triage method at Rothschild Hospital during the first lockdown due to the COVID-19 pandemic

por Saade, Yara, de la Dure Molla, Muriel, Fournier, Benjamin P. J., Kerner, Stéphane, Colon, Pierre, Carra, Maria Clotilde, Bouchard, Philippe
Publicado 2023

Oral Phenotype of Singleton–Merten Syndrome: A Systematic Review Illustrated With a Case Report

por Riou, Margot Charlotte, de La Dure-Molla, Muriel, Kerner, Stéphane, Rondeau, Sophie, Legendre, Adrien, Cormier-Daire, Valerie, Fournier, Benjamin P. J.
Publicado 2022

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 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 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 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 2014

Lack of FAM20A, Ectopic Gingival Mineralization and Chondro/Osteogenic Modifications in Enamel Renal Syndrome

por Simancas Escorcia, Victor, Diarra, Abdoulaziz, Naveau, Adrien, Dessombz, Arnaud, Felizardo, Rufino, Cannaya, Vidjeacoumary, Chatziantoniou, Christos, Quentric, Mickaël, Vikkula, Miikka, Cases, Olivier, Berdal, Ariane, De La Dure-Molla, Muriel, Kozyraki, Renata
Publicado 2020

SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects

por Dubail, Johanne, Huber, Céline, Chantepie, Sandrine, Sonntag, Stephan, Tüysüz, Beyhan, Mihci, Ercan, Gordon, Christopher T., Steichen-Gersdorf, Elisabeth, Amiel, Jeanne, Nur, Banu, Stolte-Dijkstra, Irene, van Eerde, Albertien M., van Gassen, Koen L., Breugem, Corstiaan C., Stegmann, Alexander, Lekszas, Caroline, Maroofian, Reza, Karimiani, Ehsan Ghayoor, Bruneel, Arnaud, Seta, Nathalie, Munnich, Arnold, Papy-Garcia, Dulce, De La Dure-Molla, Muriel, Cormier-Daire, Valérie
Publicado 2018

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 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 2013