Identifying the unmet health needs of patients with congenital hypogonadotropic hypogonadism using a web-based needs assessment: implications for online interventions and peer-to-peer support
Patients with rare diseases such as congenital hypogonadotropic hypogonadism (CHH) are dispersed, often challenged to find specialized care and face other health disparities. The internet has the potential to reach a wide audience of rare disease patients and can help connect patients and specialist...
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Veröffentlicht in: | Orphanet journal of rare diseases 2014-06, Vol.9 (1), p.83-83 |
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Format: | Artikel |
Sprache: | eng |
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