Detalhe da pesquisa
1.
A standard of care for individuals with PIK3CA-related disorders: An international expert consensus statement.
Clin Genet
; 101(1): 32-47, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34240408
2.
[Representation of the oral sphere in medical comics, the child's perception]. / Représentation de la sphère buccale dans la bande dessinée médicale, la perception de l'enfant.
Soins Pediatr Pueric
; 43(326): 39-42, 2022.
Artigo
em Francês
| MEDLINE | ID: mdl-35902151
3.
Periodontal (formerly type VIII) Ehlers-Danlos syndrome: Description of 13 novel cases and expansion of the clinical phenotype.
Clin Genet
; 100(2): 206-212, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33890303
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.
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
6.
Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta.
Hum Mol Genet
; 24(11): 3038-49, 2015 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25669657
7.
Influence of Child's Temperament on Behaviour Management Problems in the Dental Office: A Literature Review.
Children (Basel)
; 10(1)2023 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36670641
8.
Primary failure of eruption: From molecular diagnosis to therapeutic management.
J Oral Biol Craniofac Res
; 13(2): 169-176, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36654816
9.
Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop's classification.
Front Physiol
; 14: 1130175, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37228816
10.
Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.
Hum Mutat
; 32(1): 70-2, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20979233
11.
Efficacy, tolerability, and safety of an innovative medical device for improving oral accessibility during oral examination in special-needs patients: A multicentric clinical trial.
PLoS One
; 15(9): e0239898, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32986784
12.
[Primary failure of eruption: a French prospective survey among the orthodontists from the Grand Est and Bourgogne-Franche-Comté regions]. / Défauts primaires d'éruption : état des lieux auprès des spécialistes en orthopédie dento-faciale des régions Grand Est et Bourgogne-Franche-Comté.
Orthod Fr
; 90(2): 149-159, 2019 Jun.
Artigo
em Francês
| MEDLINE | ID: mdl-31241457
13.
A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta.
Front Genet
; 10: 504, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31191616
14.
Oral health related quality of life of children and adolescents affected by rare orofacial diseases: a questionnaire-based cohort study.
Orphanet J Rare Dis
; 14(1): 124, 2019 06 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31164137
15.
Rare dentin defects: Understanding the pathophysiological mechanisms of COLXVA1 mutations.
Genes Dis
; 11(5): 101303, 2024 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-38721411
16.
Protocol GenoDENT: Implementation of a New NGS Panel for Molecular Diagnosis of Genetic Disorders with Orodental Involvement.
Methods Mol Biol
; 1922: 407-452, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30838594
17.
Evaluation of safe and effective administration of nitrous oxide after a postgraduate training course.
BMC Clin Pharmacol
; 8: 3, 2008 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-18547418
18.
Evolutionary Analysis Predicts Sensitive Positions of MMP20 and Validates Newly- and Previously-Identified MMP20 Mutations Causing Amelogenesis Imperfecta.
Front Physiol
; 8: 398, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28659819
19.
Hemostatic management in pediatric patients with type I von Willebrand disease undergoing oral surgery: case report and literature review.
J Oral Maxillofac Surg
; 69(8): 2086-91, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21783000
20.
Detection of a Novel DSPP Mutation by NGS in a Population Isolate in Madagascar.
Front Physiol
; 7: 70, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26973538