Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Luciano Henrique Ferreira LIMA"'
Autor:
Luciano Henrique Ferreira LIMA, Ana Paula Cota VIANA, Giovanna Ribeiro SOUTO, Soraya de Mattos Camargo GROSSMANN, Carlos Roberto MARTINS, Hermínia Marques CAPISTRANO
Publikováno v:
RGO: Revista Gaúcha de Odontologia, Vol 70 (2022)
ABSTRACT Oral amyloidosis is a disease characterized by extracellular and irreversible deposition of amorphous and fibrillar proteins in the oral cavity, being strongly associated with Multiple Myeloma. The objective of this study is to report a case
Externí odkaz:
https://doaj.org/article/3bcf209daa1b41b98a5941dc46257919
Autor:
Fernanda Brasil Daura Jorge Boos Lima, Ana Paula Cota Viana, Luciano Henrique Ferreira Lima, Bruna Campos Ribeiro, Carlos Eduardo Assis Dutra, Glaykon Alex Vitti Stabile, Sergio Monteiro Lima Junior
Publikováno v:
Case Reports in Dentistry, Vol 2019 (2019)
The Gorlin-Goltz syndrome, nevoid basal cell carcinoma syndrome, or basal cell nevus syndrome is an autosomal dominant condition disorder with high variability expression. It presents a series of relevant clinical manifestations that suggest its diag
Externí odkaz:
https://doaj.org/article/124729e706c9409bbdd278f8ff81c34b
Autor:
Luciano Henrique Ferreira Lima, André Raymundo Di Spagna, Fernando Matheus Santana Tunel, Alexander Tadeu Sverzut
Publikováno v:
ARCHIVES OF HEALTH INVESTIGATION. 11:811-814
Introduction:An idiopathic bone cavity of the jaw is a rare pseudocyst with unclear etiology and is most commonly found in the body of the mandible. This lesion is generally asymptomatic and incidentally discovered on dental radiographs. Objetives:Th
Publikováno v:
Full Dentistry in Science. 13:81-84
Nevos melanocíticos são malformações da pele ou mucosa que consistem em uma proliferação benigna de células provenientes da crista neural e podem ser congênitas ou adquiridas, sendo esse último tipo o mais prevalente na mucosa oral. Sua mani
Autor:
Raquel Laís Ottoni Nunes, Nicole Ribeiro dos Anjos, Luciano Henrique Ferreira Lima, Ana Paula Cota Viana, Larissa de Ávila Pereira, Fábio Fernandes Borém Bruzinga, Soraya de Mattos Camargo Grossmann
Publikováno v:
Brazilian Journal of Oral Sciences. 22:e237544
Aim: The purpose of the study was to analyze the knowledge of dentists in Belo Horizonte, Brazil, about bisphosphonates and their clinical implications. Methods: A cross-sectional questionnaire-based study was conducted with a convenience sample of d
Condromatose sinovial unilateral da articulação temporomandibular após trauma local – relato de caso
Autor:
Luciano Henrique Ferreira Lima, Beneval José dos Santos Junior, Luiz Henrique de Melo Nogueira, André Vitor Alves Araújo
Publikováno v:
Full Dentistry in Science. 12:53-58
Synovial chondromatosis (SC) is a rare pathological condition that is characterized by the formation of cartilaginous nodules inside a joint cavity. It mainly affects the knee joints, hip, shoulder, and elbow, so the TMJ is rarely the target of such
Autor:
Renato Cardoso, Luciano Henrique Ferreira Lima, Eduardo da Fonseca, Manoel Santos Filho, Daniel Martins
Publikováno v:
Journal of the Brazilian College of Oral and Maxillofacial Surgery. 5:34-39
Introdução: a região mandibular apresenta um elevado índice de acometimento nos traumatismos faciais, gerando prejuízos funcionais e estéticos. Objetivo: o objetivo do presente trabalho foi traçar o perfil dos pacientes com fraturas mandibular
Autor:
Carla Lorena Santos, Luiz Henrique de Melo Nogueira, Manoel Roque Paraiso Santos Filho, Antonio Dionizio De Albuquerque Neto, Luciano Henrique Ferreira Lima
Publikováno v:
Full Dentistry in Science. 11:64-68
Autor:
Carlos Eduardo Assis Dutra, Fernanda Brasil Daura Jorge Boos Lima, Ana Paula Cota Viana, Glaykon Alex Vitti Stabile, Bruna Campos Ribeiro, Luciano Henrique Ferreira Lima, Sergio Monteiro Lima Junior
Publikováno v:
Case Reports in Dentistry, Vol 2019 (2019)
Case Reports in Dentistry
Case Reports in Dentistry
The Gorlin-Goltz syndrome, nevoid basal cell carcinoma syndrome, or basal cell nevus syndrome is an autosomal dominant condition disorder with high variability expression. It presents a series of relevant clinical manifestations that suggest its diag