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

by Steve Toupenay, Benjamin Philippe Fournier, Marie-Cécile Manière, Chantal Ifi-Naulin, Ariane Berdal, Muriel de La Dure– Molla
Published 2018-06-01

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

by Victor Simancas Escorcia, Abdoulaziz Diarra, Adrien Naveau, Arnaud Dessombz, Rufino Felizardo, Vidjeacoumary Cannaya, Christos Chatziantoniou, Mickaël Quentric, Miikka Vikkula, Olivier Cases, Ariane Berdal, Ariane Berdal, Muriel De La Dure-Molla, Muriel De La Dure-Molla, Renata Kozyraki, Renata Kozyraki
Published 2020-12-01

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

by Noeline Razanamihaja, Marie-Laure Boy-Lefèvre, Laurence Jordan, Lea Tapiro, Ariane Berdal, Muriel de la Dure-Molla, Sylvie Azogui-Levy
Published 2018-12-01

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

by Marie-Laure Boy-Lefèvre, Noéline Razanamihaja, Sylvie Azogui-Lévy, Andréa Vigneron, Laurence Jordan, Ariane Berdal, Muriel de la Dure-Molla
Published 2018-05-01

FAM20A Gene Mutation: Amelogenesis or Ectopic Mineralization?

by Guilhem Lignon, Fleur Beres, Mickael Quentric, Stephan Rouzière, Raphael Weil, Muriel De La Dure-Molla, Adrien Naveau, Renata Kozyraki, Arnaud Dessombz, Ariane Berdal, Ariane Berdal
Published 2017-05-01

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

by Lisa Friedlander, Rémy Choquet, Eva Galliani, Myriam de Chalendar, Claude Messiaen, Amélie Ruel, Marie-Paule Vazquez, Ariane Berdal, Corinne Alberti, Muriel De La Dure Molla
Published 2017-05-01

Oral health related quality of life of children and adolescents affected by rare orofacial diseases: a questionnaire-based cohort study

by Lisa Friedlander, Ariane Berdal, Priscilla Boizeau, Brigitte Alliot Licht, Marie-Cécile Manière, Arnaud Picard, Olivier Azzis, Marie-Paule Vazquez, Corinne Alberti, Muriel De La Dure Molla
Published 2019-06-01

Tracking endogenous amelogenin and ameloblastin in vivo.

by Jaime Jacques, Dominique Hotton, Muriel De la Dure-Molla, Stephane Petit, Audrey Asselin, Ashok B Kulkarni, Carolyn Winters Gibson, Steven Joseph Brookes, Ariane Berdal, Juliane Isaac
Published 2014-01-01

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

by Johanne Dubail, Céline Huber, Sandrine Chantepie, Stephan Sonntag, Beyhan Tüysüz, Ercan Mihci, Christopher T. Gordon, Elisabeth Steichen-Gersdorf, Jeanne Amiel, Banu Nur, Irene Stolte-Dijkstra, Albertien M. van Eerde, Koen L. van Gassen, Corstiaan C. Breugem, Alexander Stegmann, Caroline Lekszas, Reza Maroofian, Ehsan Ghayoor Karimiani, Arnaud Bruneel, Nathalie Seta, Arnold Munnich, Dulce Papy-Garcia, Muriel De La Dure-Molla, Valérie Cormier-Daire
Published 2018-08-01