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This section contains a collection of sources of information for people treating and caring for HAE patients who would like to study the subject in more depth. It includes overviews of forthcoming conferences, current original literature, references to reviews and consensus documents.
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Science & Education
Sources of information for doctors, carers and scientists
This section will be upgraded and contain special education and communication resources dedicated to physicians only in the near future. Please subscribe to the HAE newsletter in order to keep yourself updated.
A password is required to access some of the information provided, as it may only be made available to medical professionals. We apologise for any inconvenience.
A decision about suitable treatment for an individual patient with hereditary angioedema should only be made by physicians who are experienced in diagnosing and treating the disease. We refer particularly to the list of HAE expert centres known to us which can be contacted for specific advice.
Under no circumstances does the information provided by the HAE Network claim to be an adequate basis on which to make treatment decisions.
Please also note our disclaimer on this issue.
| Frequently inquired |
Author: Jerini AG
Source: HAE-Network Status: 3/08 |
