By Jenny [dot] Mansson [at] med [dot] lu [dot] se (Jenny Månsson) - published 16 October 2019 Cheong RY, Gabery S and Petersén Å.Journal of Huntington's disease 2019 Sep 26. doi: 10.3233/JHD-190372. [Epub ahead of print]AbstractHuntington's disease (HD) is a fatal genetic neurodegenerative disorder. It has mainly been considered a movement disorder with cognitive symptoms and these features have b

https://www.huntington-research.lu.se/article/role-hypothalamic-pathology-non-motor-features-huntingtons-disease - 2025-04-25

By Jenny [dot] Mansson [at] med [dot] lu [dot] se (Jenny Månsson) - published 8 November 2019 The latest issue of the Swedish magazine Vetenskap & Hälsa (Science & Health) includes an article on HD, about depression and apathy, which is frequent with HD patients. Irritability, depression, anxiety and deteriorated understanding for other people's expressions of emotions. The hereditary Huntington's

https://www.huntington-research.lu.se/article/article-hd-magazine-vetenskap-halsa - 2025-04-25

By Jenny [dot] Mansson [at] med [dot] lu [dot] se (Jenny Månsson) - published 23 March 2020 Åsa Petersén is appointed Wallenberg Clinical Scholar and receives a research grant of 15 million SEK over five years. Read more on The Royal Swedish Academy of Sciences’ webpage:https://www.kva.se/en/pressrum/pressmeddelanden/wallenberg-clinical-scholars-60-miljoner-kronor-i-anslag-till-forskande-lakare

https://www.huntington-research.lu.se/article/asa-petersen-appointed-wallenberg-clinical-scholar - 2025-04-25

By Jenny [dot] Mansson [at] med [dot] lu [dot] se (Jenny Månsson) - published 16 June 2020 A grant from The Swedish Brain Foundation (Hjärnfonden) of 600 000 SEK for 2020-2021 was awarded to Åsa and Sanaz as main and co-applicants for the project "The role of hypothalamic changes in ALS".  See also: The Brain Foundation webpage

https://www.huntington-research.lu.se/article/new-grant-swedish-brain-foundation - 2025-04-25

By Jenny [dot] Mansson [at] med [dot] lu [dot] se (Jenny Månsson) - published 21 September 2020 Members in the research group TNU had a joint Kick-off meeting with the collaborating research group BRAINS (i.e. TRAINS) at the Old Bishop’s House, September 15, 2020. Research updates were mixed with discussions on new and emerging techniques. A great day! Sanaz Gabery Rachel Cheong

https://www.huntington-research.lu.se/article/kick-tnu-old-bishops-house-september-15-2020 - 2025-04-25

By Jenny [dot] Mansson [at] med [dot] lu [dot] se (Jenny Månsson) - published 4 November 2020 Read about Åsa Petersén and her research at the website "Vetenskap & Hälsa" (”Science and Health”). Link to article (in Swedish only):https://www.vetenskaphalsa.se/huntingtons-sjukdom-en-fascinerande-gata/The website "Vetenskap & Hälsa" is a cooperation between Lund University, Malmö University and the he

https://www.huntington-research.lu.se/article/portrait-asa-petersen-vetenskap-halsa - 2025-04-25

By Jenny [dot] Mansson [at] med [dot] lu [dot] se (Jenny Månsson) - published 30 September 2020 On September 24, the Swedish National Huntington Meeting took place, hosted by the patients' organization RHS. The physical meeting that orginally was planned to be in Gothenburg, had to be transformed into an online event, as many other meetings this year, characterized by the COVID-19 pandemic.Active

https://www.huntington-research.lu.se/article/talks-and-virtual-lab-tour-swedish-national-hd-meeting - 2025-04-25

Published 5 November 2020 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.

https://www.huntington-research.lu.se/article/petersen-gives-several-talks-hd - 2025-04-25

Published 8 January 2021 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 sympto

https://www.huntington-research.lu.se/article/research-early-hd-symptoms-can-lead-new-treatment-strategies - 2025-04-25

By Jenny [dot] Mansson [at] med [dot] lu [dot] se (Jenny Månsson) - published 15 April 2021 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 ass

https://www.huntington-research.lu.se/article/new-publication-als-tnu-and-australian-collaborators - 2025-04-25

By Jenny [dot] Mansson [at] med [dot] lu [dot] se (Jenny Månsson) - published 30 August 2021 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 L

https://www.huntington-research.lu.se/article/important-paper-huntington-disease-gabery-et-al-acta-neuropathologica-2021 - 2025-04-25

Published 13 October 2021 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 - 2025-04-25

Published 21 October 2021 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 - 2025-04-25

Published 15 November 2021 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 - 2025-04-25

Published 17 May 2022 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-

https://www.huntington-research.lu.se/article/about-huntington-disease-swedish-radio - 2025-04-25

Published 8 August 2022 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 - 2025-04-25

Published 1 December 2022 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 - 2025-04-25

Published 9 January 2023 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 familie

https://www.huntington-research.lu.se/article/asa-petersen-elected-member-executive-committee-european-huntington-disease-network-ehdn - 2025-04-25

Published 10 March 2023 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 - 2025-04-25

Published 7 November 2023 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

https://www.huntington-research.lu.se/article/hd-webinar-22-november-2023 - 2025-04-25