Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ana Pereira da Silva"'
Autor:
Sara Duarte Sena Esteves, Ana Pereira da Silva, Miguel Bebiano Coutinho, José Manuel Abrunhosa, Cecília Almeida e Sousa
Publikováno v:
Brazilian Journal of Otorhinolaryngology, Vol 80, Iss 3, Pp 251-256 (2014)
INTRODUCTION: In children, hypoacusis, or conductive hearing loss, is usually acquired; otitis media with effusion is the most common etiology. However, in some cases this condition is congenital, ranging from deformities of the external and middle e
Externí odkaz:
https://doaj.org/article/a9cff564236940e0ab1c84cdc546ef12
Publikováno v:
Brazilian Journal of Otorhinolaryngology, Vol 82, Iss 4, Pp 479-483
ABSTRACT INTRODUCTION: Malignant tumors of the temporal bone are rare, with an estimated incidence of about 0.8-1.0 per 1,000,000 inhabitants per year. The vast majority of these tumors are squamous cell carcinomas and their treatment is eminently su
Externí odkaz:
https://doaj.org/article/e835df7ecfc7423e96a4c4ebfb16121c
Autor:
Jaime Ribeiro Filho, Silvio Caetano Alves Júnior, Maria Costa, Ray Silva de Almeida, Ana Pereira da Silva, Irwin Rose Alencar de Menezes, Henrique Douglas Melo Coutinho
Publikováno v:
Population Medicine. 5
Publikováno v:
Minerva Pediatrics.
The increase in resistance of the respiratory nasal caused by adenoid hypertrophy can condition changes in pulmonary ventilation and translate into a risk of cardiopulmonary diseases. The mean platelet volume is a marker of platelet function, associa
Publikováno v:
Acta otorrinolaringologica espanola. 72(4)
Autor:
Jorge Oliveira, Francisco Rosa, Ana Pereira da Silva, Cecília Almeida e Sousa, M. Coutinho, Cláudia Reis
Publikováno v:
Acta Otorrinolaringológica Española. 68:151-156
Objectives The aim of this study is to describe the experience of a tertiary referral centre in Portugal, of the placement of BAHA in children. Methods The authors performed a retrospective analysis of all children for whom hearing rehabilitation wit
Autor:
Cecília Almeida e Sousa, Ana Pereira da Silva, José Abrunhosa, Carla Cardoso, Sara Sena Esteves
Publikováno v:
Acta Otorrinolaringológica Española. 67:345-348
Hereditary hemorrhagic telangiectasia (HHT), also known by the eponym Osler-Weber-Rendu syndrome, is an autosomal dominant disorder characterised by the presence of multiple arteriovenous malformations (AVMs) affecting multiple organs. Many procedure
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