Search Results - "P. Escada"

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  1. 1

    Tympanic membrane perforations: the importance of etiology, size and location by Castelhano, L., Correia, F., Colaço, T., Reis, L., Escada, P.

    Published in European archives of oto-rhino-laryngology (01-09-2022)
    “…Purpose The ability to predict the degree of a conductive hearing loss caused by a tympanic membrane perforation is important for every otologist, as it may…”
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    Journal Article
  2. 2

    Nitinol versus non-Nitinol prostheses in otosclerosis surgery: a meta-analysis by Reis, L Roque, Donato, M, Almeida, G, Castelhano, L, Escada, P

    Published in Acta otorhino-laryngologica italica (01-08-2018)
    “…The aim of this study is to perform a systematic review and meta-analysis of observational studies in which hearing outcomes after primary stapes surgery have…”
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    Journal Article
  3. 3

    Further characterisation of the recently described SLC26A4 c.918+2T>C mutation and reporting of a novel variant predicted to be damaging by Gonçalves, A C, Santos, R, O'Neill, A, Escada, P, Fialho, G, Caria, H

    Published in Acta otorhino-laryngologica italica (01-06-2016)
    “…Pendred syndrome (PS) is the second most common type of autosomal recessive syndromic hearing loss (HL). It is characterised by sensorineural HL and goiter…”
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    Journal Article
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    eHealth for elderly people with balance disorders and risk of falling. A mixed methods study by Gaspar, A, Escada, P, Lapão, L

    Published in European journal of public health (20-10-2021)
    “…Background The increasing life expectancy in Europe has not always been accompanied by an increase in healthy life expectancy. The burden of chronic diseases…”
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    Caratterizzazione della mutazione SLC26A4 c.918+2T>C e report di una nuova variante potenzialmente a rischio by Gonçalves, A.C., Santos, R., O’Neill, A., Escada, P., Fialho, G., Caria, H.

    Published in Acta otorhino-laryngologica italica (01-05-2016)
    “…La sindrome di Pendred è, in ordine di frequenza, la seconda causa di ipoacusia su base genetica autosomica recessiva. Si manifesta con un ipoacusia…”
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    Journal Article
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    Caratterizzazione della mutazione SLC26A4 c.918+2T>C e report di una nuova variante potenzialmente a rischio by A.C. Gonçalves, R. Santos, A. O’Neill, P. Escada, G. Fialho, H. Caria

    Published in Acta otorhino-laryngologica italica (01-05-2016)
    “…La sindrome di Pendred è, in ordine di frequenza, la seconda causa di ipoacusia su base genetica autosomica recessiva. Si manifesta con un ipoacusia…”
    Get full text
    Journal Article