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The patient’s experience of primary ciliary dyskinesia: a systematic review
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by progressive sinopulmonary disease, with symptoms starting soon after birth. The aim of this study is to critically review, analyse, and synthesise the literature in order to understand the experiences of patient...
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| Publicado no: | Qual Life Res |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer International Publishing
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5548843/ https://ncbi.nlm.nih.gov/pubmed/28361274 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11136-017-1564-y |
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