Detalhe da pesquisa
1.
The impact of craniofacial and dental osteogenesis imperfecta manifestations on oral health-related quality of life of children and adolescents.
Clin Oral Investig;
28(3): 169, 2024 Feb 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38396299
2.
Pamidronate Therapy Increases Trabecular Bone Complexity of Mandibular Condyles in Individuals with Osteogenesis Imperfecta.
Calcif Tissue Int;
110(3): 303-312, 2022 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34677656
3.
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
4.
Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations.
BMC Med Genet;
16: 8, 2015 Feb 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25928877
5.
Identification of the first large deletion in the CLDN16 gene in a patient with FHHNC and late-onset of chronic kidney disease: case report.
BMC Nephrol;
16: 92, 2015 Jul 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26136118
6.
Gingival proteomics reveals the role of TGF beta and YAP/TAZ signaling in Raine syndrome fibrosis.
Sci Rep;
14(1): 9497, 2024 04 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38664418
7.
Carbonic anhydrase II deficiency syndrome with amelogenesis imperfecta linked to a homozygous CA2 deletion.
Intractable Rare Dis Res;
12(3): 202-205, 2023 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37662627
8.
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
9.
Phenotypic dento-osseous characterization of a Brazilian family with Familial Adenomatous Polyposis.
Arch Oral Biol;
129: 105206, 2021 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34224960
10.
Restorations after selective caries removal: 5-Year randomized trial.
J Dent;
99: 103416, 2020 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32585263
11.
Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations.
Orphanet J Rare Dis;
9: 84, 2014 Jun 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24927635
12.
In vitro study of laser diode 655 nm diagnosis of occlusal caries.
ASDC J Dent Child;
69(3): 249-53, 233, 2002.
Artigo
em Inglês
| MEDLINE
| ID: mdl-12613306