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Muriel de la DURE-MOLLA

PU-PH - Service d’Odontologie Hôpital Rothschild - APHP

WP1

RÉSEAU DDS CENTRÉ SUR LE PATIENT

Centre de Référence des Maladies Rares Orales et Dentaires. Paris-Rothschild
Pôles d’activités
  • Coordination du Centre de Référence des Maladies Rares Orales et Dentaires oRares
  • Prise en charge diagnostique et thérapeutique des Maladies Rares Orales et Dentaires chez l’enfant et l’adulte
  • Etablissement de guides de bonnes pratiques, consensus, PNDS
  • Pilotage de réseaux d’expertise
  • Référent auprès des autres filière et CRMR
  • Connexion avec les associations de malades, le réseau ORARES, la filière TETECOU et les réseaux européen
Projets
  • Corrélation génotype / phénotype de différentes pathologies (agénésies dentaires, incontinentia pigmenti, amélogenèse imparfaites, dentinogenèse imparfaites)
  • Caractérisation des anomalies de l’os cranio-facial chez les patients atteints d’ostéogenèse imparfaite
  • Caractérisation du phénotype dentaire de diverses maladies rares (syndrome de Gardner, dysplasie ostéoglophonique …)
Publications récentes
  • Translation and validation of the French version of the child perceptions questionnaire for children aged 11 to 14 years old (CPQ11-14) short-form. Clin Oral Investig. 2024 Jun 28;28(7):403. doi: 10.1007/s00784-024-05793-1.PMID: 38940970
  • Root resorptions induced by genetic disorders: A systematic review.Oral Dis. 2024 Sep;30(6):3799-3812. doi: 10.1111/odi.14942. Epub 2024 Apr 2.PMID: 38566363.
  • La dent : un marqueur d’anomalies génétiques du développement .  Publié en ligne : 1 février 2024 DOI: https://doi.org/10.1051/medsci/2023190
  • Unequal Impact of COL1A1 and COL1A2 Variants on Dentinogenesis Imperfecta . J Dent Res. 2023 Mar 23. doi: 10.1177/00220345231154569. PMID: 36951356
  • The dental triage method at Rothschild Hospital during the first lockdown due to the COVID-19 pandemic. PLoS One. 2023 Feb. doi: 10.1371/journal.pone.0281390.
  • Oral Phenotype of Singleton-Merten Syndrome: A Systematic Review Illustrated With a Case Report. Front Genet. 2022. PMID: 35754802
  • International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia. Nat Rev Endocrinol. 2022 Mar. PMID: 34837063
  • Multidisciplinary consensus recommendations from a European network for the diagnosis and practical management of patients with incontinentia pigmenti. JEADV 2020,  doi: 10.1111/jdv.16403.
  • Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders. Am J Med Genet A. 2019.  doi: 10.1002/ajmg.a.61316
  • Oral health related quality of life of children and adolescents affected by rare orofacial diseases: a questionnaire-based cohort study. MD. Orphanet J Rare Dis. 2019. PMID: 31164137  
  • Management of rare diseases of the Head, Neck and Teeth: results of a French population-based prospective 8-year study. Orphanet J Rare Dis. 2017. PMID: 28526043
  • Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations. J Med Genet 2017. PMID: 27530400
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FHU DDS Federation Hospitalo-Universitaire Dental Diseases - Parisnet

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