Gilberto Tenório Wanderley Fernandes Lima
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Gilberto Tenório Wanderley Fernandes Lima has a total of 18 co-authors. Here are the top co-authors by number of shared publications:
- Allan Vinícius Martins-De-Barros
Universidade de Pernambuco
3 shared publications - Fábio Andrey da Costa Araújo
University of Pernambuco, Brazil
3 shared publications - José Rodrigues Laureano Filho
Programa de Pós-Graduação em Odontologia, Campus Santo Amaro, Universidade de Pernambuco, Recife, Brazil; Hospital dos Servidores do Estado de Pernambuco, Recife, Brazil
2 shared publications - Maria Eduarda de Alencar Barreto
Programa de Pós‐Graduação em Saúde e Desenvolvimento Socioambiental Universidade de Pernambuco, Campus Arcoverde Arcoverde Brazil
2 shared publications - Pedro Henrique Sette-De-Souza
Universidade de Pernambuco
2 shared publications - Raisa Jordana Geraldine Severino-Lazo
Oral Histopathology Research Group, Graduate Program in Dentistry, Faculty of Dentistry of Pernambuco (FOP/UPE) University of Pernambuco Recife PE Brazil
2 shared publications
Latest Publications
- 11 July 2026
- Published by Elsevier in The Journal of the American Dental Association
A slow-growing nodule in the maxilla
- 11 July 2026
- Published by Elsevier in The Journal of the American Dental Association
A slow-growing nodule in the maxilla
- 1 July 2026
- Published by Wiley in Orthodontics & Craniofacial Research
- Vol. 29 (6) , 1125-1133
Is Smartphone‐Based 3D Photogrammetry Suitable for Indirect Facial Analysis in Patients With Dentofacial Deformities? A Trueness and Precision Analysis
Objective: To evaluate the trueness and precision of Qlone Dental Pro 3D Scanner for smartphones when applied to indirect facial analysis of individuals undergoing orthognathic surgical planning. Materials and Methods: This is a cross‐sectional trueness and precision study. The study population comprised individuals with dentofacial deformities. A control group without dentofacial deformity was included for comparison. Direct facial anthropometry using a digital calliper served as standard‐reference. 3D facial models in. OBJ format were obtained by Qlone Dental Pro 3D Scanner and imported to MeshLab 2025.7 where indirect facial measurements were performed. Trueness was defined by the proximity of indirect and direct facial measurements, while precision was assessed through comparison of indirect measurements from two subsequent smartphone‐based scans. Statistical analysis was performed with Jamovi 2.6.26.0. Results: The study included 40 participants, equally distributed between dentofacial deformity and control groups. In trueness analysis, mean differences ranged from −3.32 mm to 0.83 mm, with an overall mean difference of −1.47 mm. Systematic bias was statistically significant ( p < 0.05) for all measurements, except for N–Sn . Precision analysis demonstrated mean differences < 0.40 mm, with an overall mean difference of 0.14 mm, without statistically significant systematic bias ( p > 0.05). Comparison of trueness and precision between individuals with and without dentofacial deformities revealed no statistically significant differences for most measurements. Conclusion: Indirect facial anthropometric analysis using Qlone Dental Pro 3D Scanner demonstrated high precision but limited trueness compared with conventional direct measurements. The presence of dentofacial deformity did not significantly influence indirect measurement performance.
- 1 July 2026
- Published by Wiley in Orthodontics & Craniofacial Research
- Vol. 29 (6) , 1125-1133
Is Smartphone‐Based 3D Photogrammetry Suitable for Indirect Facial Analysis in Patients With Dentofacial Deformities? A Trueness and Precision Analysis
Objective: To evaluate the trueness and precision of Qlone Dental Pro 3D Scanner for smartphones when applied to indirect facial analysis of individuals undergoing orthognathic surgical planning. Materials and Methods: This is a cross‐sectional trueness and precision study. The study population comprised individuals with dentofacial deformities. A control group without dentofacial deformity was included for comparison. Direct facial anthropometry using a digital calliper served as standard‐reference. 3D facial models in. OBJ format were obtained by Qlone Dental Pro 3D Scanner and imported to MeshLab 2025.7 where indirect facial measurements were performed. Trueness was defined by the proximity of indirect and direct facial measurements, while precision was assessed through comparison of indirect measurements from two subsequent smartphone‐based scans. Statistical analysis was performed with Jamovi 2.6.26.0. Results: The study included 40 participants, equally distributed between dentofacial deformity and control groups. In trueness analysis, mean differences ranged from −3.32 mm to 0.83 mm, with an overall mean difference of −1.47 mm. Systematic bias was statistically significant ( p < 0.05) for all measurements, except for N–Sn . Precision analysis demonstrated mean differences < 0.40 mm, with an overall mean difference of 0.14 mm, without statistically significant systematic bias ( p > 0.05). Comparison of trueness and precision between individuals with and without dentofacial deformities revealed no statistically significant differences for most measurements. Conclusion: Indirect facial anthropometric analysis using Qlone Dental Pro 3D Scanner demonstrated high precision but limited trueness compared with conventional direct measurements. The presence of dentofacial deformity did not significantly influence indirect measurement performance.
- Open Access
- 4 June 2026
- Published by Elsevier in Journal of Oral Biology and Craniofacial Research
- Vol. 16 (4) , 101477
Is there a role for impaired DNA mismatch repair system in the pathogenesis of ameloblastomas? A scoping review
- 4 June 2026
- Published by Elsevier in Journal of Oral Biology and Craniofacial Research
- Vol. 16 (4) , 101477
Open AccessIs there a role for impaired DNA mismatch repair system in the pathogenesis of ameloblastomas? A scoping review
- Open Access
- 17 March 2021
- Published by Universidade de São Paulo. Agência de Bibliotecas e Coleções Digitais in Revista de Medicina
- Vol. 100 (1) , 90-93
Polipose gástrica: relato de caso e revisão da literatura
Pólipos gastrointestinais são elevações da mucosa circundante do sistema digestório, encontradas frequentemente em exames endoscópicos de rotina. A grande maioria é achado acidental e alguns pólipos podem indicar doença ou síndrome associada. Este artigo tem como objetivo apresentar um caso de polipose gástrica manifestada como Síndrome de Peütz-Jeghers em uma paciente de 25 anos, do sexo feminino, com história de dor abdominal em região epigástrica há 12 dias da admissão hospitalar, que evoluiu com vômitos e hematêmese 3 dias antes do internamento. A paciente realizou endoscopia digestiva alta (EDA), que evidenciou múltiplas lesões polipoides, regulares e de superfície lisa. Tomografia computadorizada (TC) do abdômen visualizou volumosa lesão vegetante coraliforme, de 16,3 x 10,2 x 5,4cm. Optou-se por realizar uma gastrectomia total com reconstrução em Y-de-Roux. O tempo total da cirurgia foi de 150min e ocorreu sem complicações. Paciente evoluiu com boas condições clínicas, sem intercorrências e recebeu alta hospitalar no 9º dia de pós-operatório (DPO). Estudo histopatológico da peça cirúrgica (estômago) evidenciou múltiplos pólipos gástricos de padrão predominante hamartomatoso, com transformação adenomatosa focal, margens cirúrgicas livres, sugerindo síndrome de Peütz-Jeghers. Nossa paciente não demonstrou hiperpigmentação mucocutânea, corroborando o fato de que a hiperpigmentação não é condição “sine qua non” para a síndrome de Peütz-Jeghers.
- 17 March 2021
- Published by Universidade de São Paulo. Agência de Bibliotecas e Coleções Digitais in Revista de Medicina
- Vol. 100 (1) , 90-93
Open AccessPolipose gástrica: relato de caso e revisão da literatura
Pólipos gastrointestinais são elevações da mucosa circundante do sistema digestório, encontradas frequentemente em exames endoscópicos de rotina. A grande maioria é achado acidental e alguns pólipos podem indicar doença ou síndrome associada. Este artigo tem como objetivo apresentar um caso de polipose gástrica manifestada como Síndrome de Peütz-Jeghers em uma paciente de 25 anos, do sexo feminino, com história de dor abdominal em região epigástrica há 12 dias da admissão hospitalar, que evoluiu com vômitos e hematêmese 3 dias antes do internamento. A paciente realizou endoscopia digestiva alta (EDA), que evidenciou múltiplas lesões polipoides, regulares e de superfície lisa. Tomografia computadorizada (TC) do abdômen visualizou volumosa lesão vegetante coraliforme, de 16,3 x 10,2 x 5,4cm. Optou-se por realizar uma gastrectomia total com reconstrução em Y-de-Roux. O tempo total da cirurgia foi de 150min e ocorreu sem complicações. Paciente evoluiu com boas condições clínicas, sem intercorrências e recebeu alta hospitalar no 9º dia de pós-operatório (DPO). Estudo histopatológico da peça cirúrgica (estômago) evidenciou múltiplos pólipos gástricos de padrão predominante hamartomatoso, com transformação adenomatosa focal, margens cirúrgicas livres, sugerindo síndrome de Peütz-Jeghers. Nossa paciente não demonstrou hiperpigmentação mucocutânea, corroborando o fato de que a hiperpigmentação não é condição “sine qua non” para a síndrome de Peütz-Jeghers.