Buscar
Mostrando ítems 1-10 de 15
Fibroma Oscificante: reporte de un casoFibroma Oscificante: reporte de un caso
(Facultad de Odontología, 2010)
Osteofibroma periférico.Peripheral ossifying fibroma.
(SABER ULA, 2008)
Localized gingival enlargement associated with alveolar process expansion: Peripheral ossifying fibroma coincident with central odontogenic fibroma
(Amer Acad PeriodontologyChicagoEUA, 2007)
Osteofibroma periférico.Peripheral ossifying fibroma.
(SABER ULA, 2008)
Etiopatogenia del fibroma osificante.
(Universidad de Guayaquil. Facultad Piloto de Odontología., 2015-06)
La etiopatogenia del Fibroma Osificante se manifiesta principalmente por el remplazo de tejido óseo normal por tejido conjuntivo fibroso con focos de calcificación en su interior que puede ser hueso o cemento. Son lesiones ...
Expression of odontogenic ameloblast-associated protein, amelotin, ameloblastin, and amelogenin in odontogenic tumors: immunohistochemical analysis and pathogenetic considerations
(Wiley-Blackwell, 2012-03-01)
Screening for expression of amelogenesis-related proteins represents a powerful molecular approach to characterize odontogenic tumors and investigate their pathogenesis. In this study, we have examined the presence and ...
Expression of odontogenic ameloblast-associated protein, amelotin, ameloblastin, and amelogenin in odontogenic tumors: immunohistochemical analysis and pathogenetic considerations
(Wiley-Blackwell, 2012-03-01)
Screening for expression of amelogenesis-related proteins represents a powerful molecular approach to characterize odontogenic tumors and investigate their pathogenesis. In this study, we have examined the presence and ...
Carcinoma escamocelular de labio superior en paciente con síndrome nevoide basocelular. Reporte de caso clínico / Upper Lip Squamous Cell Carcinoma in Patient with Basal Cell Nevus Syndrome. Case Report
RESUMEN. Antecedentes: El síndrome de Gorlin-Goltz, o síndrome nevoide de células basales (SNCB), es un trastorno autosómico dominante de baja incidencia. Su etiología está relacionada con una mutación en el gen PTCH y ...