Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Muriel de La Dure– Molla"'
Autor:
Steve Toupenay, Benjamin Philippe Fournier, Marie-Cécile Manière, Chantal Ifi-Naulin, Ariane Berdal, Muriel de La Dure– Molla
Publikováno v:
BMC Oral Health, Vol 18, Iss 1, Pp 1-8 (2018)
Abstract Background Hereditary enamel defect diseases are regrouped under the name “Amelogenesis Imperfecta” (AIH). Both dentitions are affected. Clinical expression is heterogeneous and varies between patients. Mutations responsible for this mul
Externí odkaz:
https://doaj.org/article/f88ece5436374416ae289587779c0737
Autor:
Agnes Bloch-Zupan, Tristan Rey, Alexandra Jimenez-Armijo, Marzena Kawczynski, Naji Kharouf, O-Rare consortium, Muriel de La Dure-Molla, Emmanuelle Noirrit, Magali Hernandez, Clara Joseph-Beaudin, Serena Lopez, Corinne Tardieu, Béatrice Thivichon-Prince, ERN Cranio Consortium, Tatjana Dostalova, Milan Macek, International Consortium, Mustapha El Alloussi, Leila Qebibo, Supawich Morkmued, Patimaporn Pungchanchaikul, Blanca Urzúa Orellana, Marie-Cécile Manière, Bénédicte Gérard, Isaac Maximiliano Bugueno, Virginie Laugel-Haushalter, Yves Alembik, Victorin Ahossi, Isabelle Bailleul-Forestier, Isabelle Blanchet, Ariane Berdal, Marie José Boileau, Nicolas Chassaing, François Clauss, Caroline Delfosse, Anne De-Saint-Martin, Jean-Christophe Dahlet, Bérénice Doray, Jean-Luc Davideau, Tiphaine Davit-Béal, Hélène Dollfus, Jean-Pierre Duprez, Muriel de La Dure Molla, Klauss Dieterich, Dominique Droz, Salima El Chehadeh, Olivier Etienne, Edouard Euvrard, Laurence Faivre, Benjamin Fournier, Elsa Garot, Bruno Grollemund, Nathalie Guffon-Fouilhoux, Mathilde Huckert, Bertand Isidor, Sophie Jung, Didier Lacombe, Alinoe Lavillaurex, Marine Lebrun, Bruno Leheup, Adeline Loing, Sandrine Marlin, Jean-Jacques Morrier, Michèle Muller-Bolla, Sylvie Odent, Marie Paule Gelle, Juliette Piard, Linda Pons, Béatrice Richard, Massimiliano Rossi, Prune Sadones, Elise Schaefer, Jean-Louis Sixou, Sylvie Soskin, Marion Strub, Annick Toutain, Alain Verloes, Frédéric Vaysse, Delphine Wagner
Publikováno v:
Frontiers in Physiology, Vol 14 (2023)
Amelogenesis imperfecta (AI) is a heterogeneous group of genetic rare diseases disrupting enamel development (Smith et al., Front Physiol, 2017a, 8, 333). The clinical enamel phenotypes can be described as hypoplastic, hypomineralized or hypomature a
Externí odkaz:
https://doaj.org/article/be19745ebc994351a79834498f898534
Autor:
Yara Saade, Muriel de la Dure Molla, Benjamin P J Fournier, Stéphane Kerner, Pierre Colon, Maria Clotilde Carra, Philippe Bouchard
Publikováno v:
PLoS ONE, Vol 18, Iss 2, p e0281390 (2023)
ObjectiveThis study aims to (1) assess the efficacy of a face-to-face emergency protocol in children and adults and (2) measure the efficacies of prediagnosis at the triage level and clinical diagnosis at the emergency department level during the COV
Externí odkaz:
https://doaj.org/article/b31b699cad9f4bbbaa6400933c6e262f
Autor:
Charlotte Guillouet, Margot C. Riou, Lucas T. Duong, Muriel de La Dure-Molla, Benjamin P. J. Fournier
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Oral mucosal lesions are common in the pediatric population and, apart from traumatic and tumoral etiologies, they can be symptoms of viral, bacterial, fungal or parasitic diseases. Yet, pediatricians and pediatric dentists find it challenging to rea
Externí odkaz:
https://doaj.org/article/4ae28e80b86043228a63f3bb66c3943e
Autor:
Margot Charlotte Riou, Muriel de La Dure-Molla, Stéphane Kerner, Sophie Rondeau, Adrien Legendre, Valerie Cormier-Daire, Benjamin P. J. Fournier
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Singleton–Merten syndrome type 1 (SGMRT1) is a rare autosomal dominant disorder caused by IFIH1 variations with blood vessel calcifications, teeth anomalies, and bone defects.Aim: We aimed to summarize the oral findings in SGMRT1 throug
Externí odkaz:
https://doaj.org/article/41e8a73ba13a4718821b4f8562325c78
Autor:
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
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-13 (2019)
Abstract Background Rare diseases affecting the teeth, the oral cavity and the face are numerous, each of them present specific characteristics, and is a life-long condition. The aim of the study was to assess the association between Oral health-rela
Externí odkaz:
https://doaj.org/article/da9f61b558854fd58c1c3c84873b1ad7
Autor:
Victor Simancas Escorcia, Abdoulaziz Diarra, Adrien Naveau, Arnaud Dessombz, Rufino Felizardo, Vidjeacoumary Cannaya, Christos Chatziantoniou, Mickaël Quentric, Miikka Vikkula, Olivier Cases, Ariane Berdal, Muriel De La Dure-Molla, Renata Kozyraki
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Enamel renal syndrome (ERS) is a rare recessive disorder caused by loss-of-function mutations in FAM20A (family with sequence similarity 20 member A, OMIM #611062). Enamel renal syndrome is characterized by amelogenesis imperfecta, delayed or failed
Externí odkaz:
https://doaj.org/article/406c84b6f3bc4895964e613dd15074e0
Autor:
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
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-13 (2017)
Abstract Background In the last ten years, national rare disease networks have been established in France, including national centres of expertise and regional ones, with storage of patient data in a bioinformatics tool. The aim was to contribute to
Externí odkaz:
https://doaj.org/article/799b71fc01f84966a833731c3a1ef7ee
Autor:
Muriel de La Dure-Molla, Kemelly Karolliny Resende, Margot Charlotte Riou, Paulo Marcio Yamaguti, Benjamin Fournier, Sophie Rondeau, Laurence Pacot, Ariane Berdal, Juliana Mazzeu, Valérie Cormier-Daire, Céline Gaucher, Ana Acevedo
Amelogenesis imperfecta (AI) is a group of rare genetic conditions characterized by quantitative and/or qualitative tooth enamel alterations. AI can manifest as an isolated trait or as part of a syndrome. Recently, five biallelic disease-causing vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb9380d3566b949d2fb928e0e676e3ca
https://doi.org/10.21203/rs.3.rs-2534719/v1
https://doi.org/10.21203/rs.3.rs-2534719/v1
Autor:
Pascal Garrec, Maria Clotilde Carra, Rufino Felizardo, Muriel De La Dure-Molla, Marie-Laure Boy-Lefèvre, Laurence Jordan, Benjamin Fournier, Noeline Razanamihaja, Brigitte Vi-Fane, Nicole Beydon, Stéphane Kerner
Publikováno v:
Sleep Medicine
Sleep Medicine, Elsevier, 2019, 58, pp.123-129. ⟨10.1016/j.sleep.2019.02.021⟩
Sleep Medicine, Elsevier, 2019, 58, pp.123-129. ⟨10.1016/j.sleep.2019.02.021⟩
International audience; Background: Sleep-disordered breathing (SDB), including obstructive sleep apnea syndrome, is often underestimated because it requires a burdensome test (ie, polysomnography) to ensure diagnosis. To improve polysomnography refe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::886505ca00639dc108ed408b4ddf11b2
https://doi.org/10.1016/j.sleep.2019.02.021
https://doi.org/10.1016/j.sleep.2019.02.021