Public information evening on HD

2023-01-17
Twice a year we host an information evening on Huntington disease open to the public. Staff from the clinical team, as well as HD researchers give talks about the disease and the current research. And there will be fika, of course! On Monday 15 May at 18.00-20.30 the spring meeting will take place at the Biomedical Centre in Lund. More information will come!
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Åsa Petersén elected member of the executive committee for the European Huntington Disease Network (EHDN)

2023-01-09
Åsa Petersén has been elected member of the executive committee for the European Huntington Disease Network (EHDN). The EHDN is a nonprofit research network committed to advancing research, facilitating the conduct of clinical trials, and improving clinical care in HD. Through the EHDN a platform has been created such that basic scientists, clinicians, patients and families can collaborate on academic and industry studies to fulfil its mission. The EHDN is supported by and collaborates closely…
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