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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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| Pubblicato in: | Qual Life Res |
|---|---|
| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Springer International Publishing
2017
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| Soggetti: | |
| Accesso online: | 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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