Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Telma Feliciano"'
Autor:
Ângela Reis Rego, David Dias, Ana Pinto, Sandra Sousa e Castro, Telma Feliciano, Cecília Almeida e Sousa
Publikováno v:
Journal of Otology, Vol 14, Iss 2, Pp 51-56 (2019)
Introduction: MD is considered a rare disease. An adequate model that explains MD's pathophysiology is not well established. Recently, the vascular theory of the disease has been revived. Objectives: To characterize a MD population according to its c
Externí odkaz:
https://doaj.org/article/76dfba844c97496bb4c198cf13fd0793
Autor:
Ana Rodrigues, Francisco Alves de Sousa, Maria J Casanova, Ana Silva, Telma Feliciano, Susana Vaz Freitas, Ricardo Pinto, João Lino
Publikováno v:
Cureus.
Publikováno v:
An International Journal of Otorhinolaryngology Clinics. 13:61-63
Autor:
Cecília Almeida e Sousa, Sandra Sousa e Castro, Telma Feliciano, David Dias, Ângela Reis Rego, Ana Nóbrega Pinto
Publikováno v:
Journal of Otology, Vol 14, Iss 2, Pp 51-56 (2019)
Journal of Otology
Journal of Otology
Introduction: MD is considered a rare disease. An adequate model that explains MD's pathophysiology is not well established. Recently, the vascular theory of the disease has been revived. Objectives: To characterize a MD population according to its c
Publikováno v:
Medical Hypotheses. 100:43-45
Cholesteatoma is a common clinical picture seen by otolaryngologists. The disease is characterised by an abnormal grow “of skin in the wrong place”. Specifically, in acquired cholesteatoma, the main causative issue is associated with ventilatory
Autor:
Isabel Carvalho, Susana Vaz Freitas, Pedro Carvalho Santos, Telma Feliciano, Pedro Henriques Santos, Cecília Almeida, Ângela Reis-Rego, David Dias, Miguel Bebiano Coutinho, Gustavo Santos
Publikováno v:
Journal of voice : official journal of the Voice Foundation. 33(4)
The aim of this case-control study was to evaluate the overall behavior of children with vocal fold nodules (VNs).The study group included children with VNs between 4 and 15 years old diagnosed using fiberoptic video laryngoscopy with stroboscopy in
Publikováno v:
Acta Otorrinolaringológica Española. 64:423-427
Resumen La osteogenesis imperfecta es la enfermedad hereditaria del tejido conectivo mas frecuente. Su presentacion clinica tiene un amplio espectro de caracteristicas que incluyen deformidades esqueleticas e hipoacusia. Se describen 3 casos clinicos
Publikováno v:
Acta Otorrinolaringologica (English Edition). 64:423-427
Osteogenesis imperfecta is the commonest connective tissue hereditary disease. Its clinical presentation has a wide spectrum of characteristics, which includes skeletal deformities and hearing loss. We describe three case reports of individuals carri
Autor:
Susana Vaz Freitas, Ana Pereira da Silva, Telma Feliciano, Cecília Almeida e Sousa, Sara Sena Esteves
Publikováno v:
Journal of voice : official journal of the Voice Foundation. 29(3)
Summary Background Laryngeal carcinoma accounts for about 80 000 deaths annually worldwide. Despite its aggressiveness, total laryngectomy (TL) is a treatment option with curative intent. This article aims to evaluate its impact on these patients qua
Publikováno v:
Acta otorrinolaringologica espanola. 64(6)
Osteogenesis imperfecta is the commonest connective tissue hereditary disease. Its clinical presentation has a wide spectrum of characteristics, which includes skeletal deformities and hearing loss. We describe three case reports of individuals carri