Detalhe da pesquisa
1.
Root resorptions induced by genetic disorders: A systematic review.
Oral Dis
; 2024 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38566363
2.
Reduced bone dimension in patients affected by oligodontia: A retrospective study on maxillary and mandibular CBCT.
J Clin Periodontol
; 50(12): 1590-1600, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37653705
3.
Replacement of missing lateral incisors for patients with cleft lip and palate: A decision-making tree based on a systematic review of the literature.
J Prosthet Dent
; 2023 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37679238
4.
Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders.
Am J Med Genet A
; 179(10): 1913-1981, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31468724
5.
Translation and validation of the French version of the Child Perceptions Questionnaire for children aged from 8 to 10 years old (CPQ 8-10).
Health Qual Life Outcomes
; 16(1): 86, 2018 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29720198
6.
Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations.
J Med Genet
; 54(1): 26-37, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27530400
7.
Parental-Caregivers Perceptions Questionnaire (P-CPQ): translation and evaluation of psychometric properties of the French version of the questionnaire.
BMC Oral Health
; 18(1): 211, 2018 12 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30537964
8.
Amelogenesis imperfecta: therapeutic strategy from primary to permanent dentition across case reports.
BMC Oral Health
; 18(1): 108, 2018 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29907114
9.
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement.
J Med Genet
; 53(2): 98-110, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26502894
10.
[Enamel: a unique self-assembling in mineral world]. / L'émail - Un autoassemblage unique dans le monde du minéral.
Med Sci (Paris)
; 31(5): 515-21, 2015 May.
Artigo
em Francês
| MEDLINE | ID: mdl-26059302
11.
Enamel defects reflect perinatal exposure to bisphenol A.
Am J Pathol
; 183(1): 108-18, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23764278
12.
Ameloblastin as a putative marker of specific bone compartments.
Connect Tissue Res
; 55 Suppl 1: 117-20, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25158194
13.
[The tooth: A marker of developmental abnormalities]. / La dent : un marqueur d'anomalies génétiques du développement.
Med Sci (Paris)
; 40(1): 16-23, 2024 Jan.
Artigo
em Francês
| MEDLINE | ID: mdl-38299898
14.
The dental triage method at Rothschild Hospital during the first lockdown due to the COVID-19 pandemic.
PLoS One
; 18(2): e0281390, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36753528
15.
Oro-dental phenotyping and report of three families with RELT-associated amelogenesis imperfecta.
Eur J Hum Genet
; 31(11): 1337-1341, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37670079
16.
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations.
Nephron Physiol
; 122(1-2): 1-6, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23434854
17.
Oral Phenotype of Singleton-Merten Syndrome: A Systematic Review Illustrated With a Case Report.
Front Genet
; 13: 875490, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35754802
18.
Oral lesions of viral, bacterial, and fungal diseases in children: A decision tree.
Front Pediatr
; 10: 937808, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35958174
19.
Gingival inflammation, enamel defects, and tooth sensitivity in children with amelogenesis imperfecta: a case-control study.
J Appl Oral Sci
; 28: e20200170, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32997085
20.
Lack of FAM20A, Ectopic Gingival Mineralization and Chondro/Osteogenic Modifications in Enamel Renal Syndrome.
Front Cell Dev Biol
; 8: 605084, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33425910