Search filters

List of works by Muriel de la Dure Molla

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

scientific article published on 26 October 2015

Ameloblastin as a putative marker of specific bone compartments.

scientific article

Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations

scientific article

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

scientific article published on 15 June 2018

Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders

scientific article published on 29 August 2019

Enamel: a unique self-assembling in mineral world

scientific article published in May 2015

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

scientific article published on 28 September 2020

Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification

scientific article published on 13 August 2014

MSX2 in ameloblast cell fate and activity

scientific article

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations ⬇️

scientific article

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

scientific article

Tracking endogenous amelogenin and ameloblastin in vivo ⬇️

scientific article

Treatment of infra-occluded primary molars in patients with dental ageneses

scientific article published on 03 August 2014

Paulina is supported by:

About Paulina

Help