Brain hypoxia and metabolic crisis are common in patients with acute brain injury despite a normal intracranial pressure.

Autor: Lund, Anton¹ (AUTHOR) anton.lund@regionh.dk, Madsen, Anna Forsberg¹ (AUTHOR), Capion, Tenna² (AUTHOR), Jensen, Helene Ravnholt¹ (AUTHOR), Forsse, Axel² (AUTHOR), Hauerberg, John² (AUTHOR), Sigurðsson, Sigurður Þor¹ (AUTHOR), Mathiesen, Tiit Illimar^2,3,4 (AUTHOR), Møller, Kirsten^1,3 (AUTHOR), Olsen, Markus Harboe¹ (AUTHOR)

Publikováno v: Scientific Reports. 10/11/2024, Vol. 14 Issue 1, p1-12. 12p.

Targeted Treatment of Metastatic Triple‐Negative Breast Cancer: A Systematic Review.

Autor: Hammershøi Madsen, Anna Martha¹ anna.h.madsen@sund.ku.dk, Løvendahl Eefsen, Rikke Helene¹, Nielsen, Dorte¹, Kümler, Iben¹, Yang, Guan-Jun¹

Publikováno v: Breast Journal. 7/11/2024, Vol. 2024, p1-15. 15p.

Återhämtningsprocessen hos en svensk livsmedelsproducent efter ett allvarligt produktfel : En studie av Findus hantering av 'Hästköttsskandalen' under våren 2013

Autor: Grujicic, Misel, Madsen, Anna

This study deals with a Swedish company in a food industry that got affected by product failure, which led to consumer trust crisis followed by media and was needed to be managed. Situation had a negative impact on company’s trademark, which acquir

Externí odkaz: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-104693

National Development: (Too) High Termination Fees? (Denmark).

Autor: Plum, Jens Munk, Orbaek, Andreas Juel, Madsen, Anna Yao Xi

Publikováno v: Journal of European Competition Law & Practice; Oct2023, Vol. 14 Issue 7, p430-436, 7p

Genotype and phenotype classification of 29 patients affected by Krabbe disease

Autor: Madsen, Anna M H, Wibrand, Flemming, Lund, Allan M, Ek, Jakob, Dunø, Morten, Østergaard, Elsebet

Publikováno v: JIMD Reports
Madsen, A M H, Wibrand, F, Lund, A M, Ek, J, Dunø, M & Østergaard, E 2019, ' Genotype and phenotype classification of 29 patients affected by Krabbe disease ', JIMD Reports, vol. 46, no. 1, pp. 35-45 . https://doi.org/10.1002/jmd2.12007

Krabbe disease is a rare neurodegenerative lysosomal storage disorder caused by mutations in the galactocerebrosidase gene, GALC. Krabbe disease usually affects infants, but has also been reported in older children and adults. Different phenotypes ar

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::cfd708d1f820db61407a3dd4ea4875bd
http://europepmc.org/articles/PMC6498822