Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ana, Pereira da Silva"'
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
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:
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
Autor:
Cecília Almeida e Sousa, Ana Pereira da Silva, José Abrunhosa, Miguel Bebiano Coutinho, Sara Sena Esteves
Publikováno v:
International Journal of Pediatric Otorhinolaryngology Extra. 10:11-13
Craniometaphyseal dysplasia is an extremely rare genetic disorder characterized by dysplastic, sclerotic, and hyperostotic involvement of cranial and tubular bones. The majority of the cases are inherited via an autosomal dominant pattern. We present