Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Joaquim Felipe-Júnior"'
Autor:
Cristianne Kalinne Santos Medeiros, Glória Maria de França, Weslay Rodrigues da Silva, Joaquim Felipe Júnior, Hébel Cavalcanti Galvão, Patrícia Teixeira de Oliveira
Publikováno v:
Autopsy and Case Reports, Vol 12 (2022)
Verruciform xanthoma (VX) is a rare benign lesion of unknown etiology, with a rough or papillary aspect, painless, sessile, well-defined, most lesions do not exceed 2 cm in their largest diameter, the degree of keratinization of the surface influence
Externí odkaz:
https://doaj.org/article/e9e779998f45458a89e385c46bda4ca2
Autor:
Joaquim Felipe Júnior, Glória Maria de França, Caio César da Silva Barros, Fernanda Aragão Felix, Weslay Rodrigues da Silva, Hévio Freitas de Lucena, Cláudia Nunes Oliveira, Hébel Cavalcanti Galvão
Publikováno v:
Oral and maxillofacial surgery. 26(4)
Odontogenic cysts are a heterogeneous group of lesions with varied clinical behavior.To analyze the expression of the epidermal growth factor receptor (EGFR), Cyclin D1, and transcription factor SOX2 in the odontogenic epithelium evaluating the cell
Autor:
Ana Myriam Costa de Medeiros, Hébel Cavalcanti Galvão, Weslay Rodrigues da Silva, Glória Maria de França, Katianne Soares Rodrigues, Jabes Gennedyr da Cruz Lima, Joaquim Felipe-Júnior
Publikováno v:
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. 130:e173-e174
The lymphoid tissue from the body plays an important role in the recognition and processing of antigens. In response to antigen-antibody reaction, lymphoid cells proliferate, increasing in number to combat the aggressor agent more effectively, result
Autor:
Petrus Pereira Gomes, Glória Maria de França, Ana Cláudia de Macedo Andrade, Joaquim Felipe-Júnior, Luiz Carlos Moreira-Júnior, Adriano Rocha Germano, Hébel Cavalcanti Galvão
Publikováno v:
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. 130:e122-e123
Pycnodysostosis is a rare, autosomal recessive genetic condition that causes a decrease in bone remodeling due to a mutation in the cathepsin K gene, resulting in clinical and radiographic manifestations, characteristic of the syndrome. This report a