Difference between revisions of "Should Clinicians Edit Wikipedia to Engage a Wider World Web"
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+ | {{Infobox work | ||
+ | | title = Should Clinicians Edit Wikipedia to Engage a Wider World Web | ||
+ | | date = 2012 | ||
+ | | authors = [[M Kint]]<br />[[Daniel P. Hart]] | ||
+ | | doi = 10.1136/bmj.e4275 | ||
+ | | link = https://www.bmj.com/content/345/bmj.e4275 | ||
+ | }} | ||
'''Should Clinicians Edit Wikipedia to Engage a Wider World Web''' - scientific work related to [[Wikipedia quality]] published in 2012, written by [[M Kint]] and [[Daniel P. Hart]]. | '''Should Clinicians Edit Wikipedia to Engage a Wider World Web''' - scientific work related to [[Wikipedia quality]] published in 2012, written by [[M Kint]] and [[Daniel P. Hart]]. | ||
== Overview == | == Overview == | ||
The “parents’ perspective” in the clinical review on the diagnosis and management of haemophilia highlights the responsibility of clinical teams to “coach and guide” people with a newly diagnosed rare genetic condition.1 The requirement for specialist teams to provide up to date information resources for the public is increasingly challenging, with the expectation of immediate availability, as offered online. | The “parents’ perspective” in the clinical review on the diagnosis and management of haemophilia highlights the responsibility of clinical teams to “coach and guide” people with a newly diagnosed rare genetic condition.1 The requirement for specialist teams to provide up to date information resources for the public is increasingly challenging, with the expectation of immediate availability, as offered online. |
Revision as of 10:39, 15 February 2021
Authors | M Kint Daniel P. Hart |
---|---|
Publication date | 2012 |
DOI | 10.1136/bmj.e4275 |
Links | Original |
Should Clinicians Edit Wikipedia to Engage a Wider World Web - scientific work related to Wikipedia quality published in 2012, written by M Kint and Daniel P. Hart.
Overview
The “parents’ perspective” in the clinical review on the diagnosis and management of haemophilia highlights the responsibility of clinical teams to “coach and guide” people with a newly diagnosed rare genetic condition.1 The requirement for specialist teams to provide up to date information resources for the public is increasingly challenging, with the expectation of immediate availability, as offered online.