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Åsa Petersén will give several talks on HD and genetic testing at HD Education Day on November 26. The Education Day is an online event, sponsored by the National Board of Health and Welfare in Sweden. This day will be followed by a session two weeks later, where Åsa Petersén, Håkan Widner, Carina Hvalstedt and Katarina Holmsten will be online, live, to answer questions. Both Petersén and Widner a

https://www.huntington-research.lu.se/article/petersen-gives-several-talks-hd - 2025-10-05

Knut and Alice Wallenberg Foundation appointed Åsa Petersén Wallenberg Clinical Scholar in 2020. An article on Åsa's research is now published on the foundation's website. The Wallenberg Clinical Scholar is aimed for researchers combining their research with clinical work and is a grant for five years. The article on Petersén's research is presenting the psychiatric symptoms and hypothalamic chang

https://www.huntington-research.lu.se/article/research-early-hd-symptoms-can-lead-new-treatment-strategies - 2025-10-05

TNU:s study on ALS together with Australian collaborators on Lund university's top news today. Åsa Petersén, Sanaz Gabery and collaborators in Australia have, for the first time, shown changes in hypothalamic neurons regulating metabolism, sleep and emotions in ALS patients. Since long, researchers have assumed that changes in metabolism are affecting the progress of the disease. Identification of

https://www.huntington-research.lu.se/article/new-publication-als-tnu-and-australian-collaborators - 2025-10-05

TNU published a new paper on early changes in the limbic system in Huntington disease together with international collaborators in Acta Neuropathologica, August 26, 2021. Link to article (opens in a new window): Early white matter pathology in the fornix of the limbic system in Huntington disease Link to Lund University webpage for news article on the the results (in Swedish): Känslohjärnan – en n

https://www.huntington-research.lu.se/article/important-paper-huntington-disease-gabery-et-al-acta-neuropathologica-2021 - 2025-10-05

Petersén and Gabery give talks about research at the National Huntington Meeting October 13, 2021. It is a digital meeting where you can see the talks at the home page of the Swedish patient organisation RHS:  https://huntington.se/13-oktober-valkomna-pa-nationellt-mote-kring-huntingtons-sjukdom/ (Opens a new window)  

https://www.huntington-research.lu.se/article/petersen-and-gabery-give-talks-about-research-national-huntington-meeting-october-13-202 - 2025-10-05

Petersén gives talks about research and clinical care for Huntington disease to young adults in HD families at a conference in Gothenburg October 21-24, 2021. See homepage of the patient organization Swedish Huntington Association (Riksförbundet för Huntingtons sjukdom) for more information:  Link to Swedish Huntington Association's webpage (opens in a new window)

https://www.huntington-research.lu.se/article/petersen-gives-talks-conference-young-people-hd - 2025-10-05

On 11-12 November 2021 the SWEMODIS annual meeting on Parkinson’s disease and other Movement Disorders took place in Stockholm, where Åsa Petersén gave a talk on Huntington's disease. SWEMODIS webpage (opens in a new window)

https://www.huntington-research.lu.se/article/petersen-gave-talk-annual-swemodis-meeting - 2025-10-05

Huntington disease is the topic of today’s episode of the radio program Kropp & Själ, Body & Mind, on the Swedish public service radio. The dilemma of genetic testing is one of the aspects of the disease discussed in the program, where Åsa Petersén is a guest. You can access today’s episode on Sveriges Radio’s website: https://sverigesradio.se/avsnitt/huntingtons-sjukdom-den-felande-genen (in Swed

https://www.huntington-research.lu.se/article/about-huntington-disease-swedish-radio - 2025-10-05

Petersén (PI) and Gabery (co-PI) received a research grant of 1.2 MSEK from the Swedish Brain Foundation (Hjärnfonden) for a project on novel mechanisms of disease and a potential future therapy for HD. Link to the Swedish Brain Foundation's webpage  

https://www.huntington-research.lu.se/article/research-grant-swedish-brain-foundation - 2025-10-05

Petersén (PI) received a research grant of 6 MSEK from the Swedish Research Council (Vetenskapsrådet) for 2023-2026 for a project on novel cellular and molecular mechanisms in the limbic system for psychiatric symptoms in Huntington disease. 

https://www.huntington-research.lu.se/article/research-grant-swedish-research-council - 2025-10-05

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 acad

https://www.huntington-research.lu.se/article/asa-petersen-elected-member-executive-committee-european-huntington-disease-network-ehdn - 2025-10-05

Knut and Alice Wallenberg Foundation has in cooperation with Åsa Petersén produced a short film about Huntington's disease and Petersén's research on HD. Petersén was awarded Wallenberg Clinical Scholar in 2020. Link to the movie "Huntington's disease - the hunt for treatment" on YouTube  

https://www.huntington-research.lu.se/article/film-about-hd-asa-petersen - 2025-10-05

Curious about HD research and wish to learn more? The European Huntington Association/Moving Forward Team is inviting you to a webinar in Norwegian on 22 November. Astri Arnesen, the President of the European Huntington Association, will speak about international HD research, Lasse Pihlstrøm, a Norwegian HD neurologist and researcher, will address HD studies and trials in Norway, and Åsa Petersén,

https://www.huntington-research.lu.se/article/hd-webinar-22-november-2023 - 2025-10-05

The European Huntington Association/Moving Forward Team’s webinar in now available on our site! You find it under Talks & Movies:Talks & Movies

https://www.huntington-research.lu.se/article/watch-webinar - 2025-10-05

The National meeting for HD is a yearly event arranged by the patients’ organization RHS. This year, 2023, it took place in Gothenburg on 30 November. All talks at the meeting are available on RHS website; only in Swedish.You find Åsa Petersén’s research update about 13 minutes into the film. To access the video, go to RHS website:RHS website

https://www.huntington-research.lu.se/article/petersen-gives-research-update-national-meeting-hd-sweden - 2025-10-05

Every spring, Huntington Disease Center in Lund traditionally hosts an information night on Huntington disease. This year is no exception! The program is set for the evening:Staff from the clinical team and representatives from the patients’ organization, RHS, as well as HD researchers, will give talks about different aspects of the the disease and the current research. And, as always, there will

https://www.huntington-research.lu.se/article/welcome-info-night-hd-22-april-2024 - 2025-10-05

Sofia Bergh, PhD student in TNU, gave two presentations on Huntington disease on 11 and 12 March 2024 during the NMT Days.This is an annual event, arranged by the Faculty of Science, the Faculty of Medicine and the Faculty of Engineering at Lund University. A week of talks and demonstrations on a variety of topics show today’s research, and students in upper secondary school and their teachers are

https://www.huntington-research.lu.se/article/bergh-presented-nmt-days - 2025-10-05

Åsa Petersén gave a talk about Huntington disease and her research for the patients' organization, RHS, in Stockholm on 12 March 2024, where she was invited.

https://www.huntington-research.lu.se/article/petersen-gave-hd-talk-stockholm - 2025-10-05

Sofia Bergh's talk from the NMT days is now available online. See more on the Talks & Movies page.

https://www.huntington-research.lu.se/article/see-sofia-berghs-talk-hd - 2025-10-05

Sofia passed her half time review on 28 May 2024. Sofia Bergh presented her work titled "Cellular and molecular mechanisms of hypothalamic pathology in Huntington disease and the amyotrophic lateral sclerosis/frontotemporal dementia disease spectrum" before the audience and the reviewers Niels Henning Skotte, research group leader, Department for Drug Design and Pharmacology, Molecular Neuroprotec

https://www.huntington-research.lu.se/article/congratulations-sofia-bergh - 2025-10-05