Zobrazeno 1 - 10
of 107
pro vyhledávání: '"Vibeke A Larsen"'
Autor:
Grigoris Effraimidis, Åse Krogh Rasmussen, Morten Dunoe, Lis F Hasholt, Flemming Wibrand, Soren S Sorensen, Allan M Lund, Lars Kober, Henning Bundgaard, Puriya D W Yazdanfard, Peter Oturai, Vibeke A Larsen, Victor Hugo Fraga de Abreu, Lotte Hahn Enevoldsen, Tatiana Kristensen, Kirsten Svenstrup, Margrethe Bastholm Bille, Farah Arif, Mette Mogensen, Mads Klokker, Vibeke Backer, Caroline Kistorp, Ulla Feldt-Rasmussen
Publikováno v:
PLoS ONE, Vol 18, Iss 6, p e0287268 (2023)
[This corrects the article DOI: 10.1371/journal.pone.0277767.].
Externí odkaz:
https://doaj.org/article/8883cb76a9684b67b23e0587339173dc
Autor:
Grigoris Effraimidis, Åse Krogh Rasmussen, Morten Dunoe, Lis F Hasholt, Flemming Wibrand, Soren S Sorensen, Allan M Lund, Lars Kober, Henning Bundgaard, Puriya D W Yazdanfard, Peter Oturai, Vibeke A Larsen, Vitor Hugo Fraga de Abreu, Lotte Hahn Enevoldsen, Tatiana Kristensen, Kirsten Svenstrup, Margrethe Bastholm Bille, Farah Arif, Mette Mogensen, Mads Klokker, Vibeke Backer, Caroline Kistorp, Ulla Feldt-Rasmussen
Publikováno v:
PLoS ONE, Vol 17, Iss 11, p e0277767 (2022)
The lysosomal storage disorder Fabry disease is caused by deficient or absent activity of the GLA gene enzyme α-galactosidase A. In the present study we present the molecular and biochemical data of the Danish Fabry cohort and report 20 years' (2001
Externí odkaz:
https://doaj.org/article/46f76d69a186404e998ffcca330b395a
Autor:
Pardis Zarifkar, Klaus Hansen, Clarissa Crone, Kirsten Svenstrup, Vibeke Andrée Larsen, William Kristian Karlsson
Publikováno v:
Case Reports in Neurology, Vol 14, Iss 2, Pp 256-260 (2022)
A 36-year-old nullipara at 35 weeks of gestation woke up with slurred speech and dysphagia. The next day, she developed abruption of the placenta, underwent an acute cesarean, and was diagnosed with severe preeclampsia. Neurologic examination reveale
Externí odkaz:
https://doaj.org/article/79a00b05add6493abc10a0c21c7beb64
Autor:
Cecilie Videbæk, Jette Stokholm, Henrik Sengeløv, Lone U. Fjeldborg, Vibeke Andrée Larsen, Christian Krarup, Jørgen E. Nielsen, Sabine Grønborg
Publikováno v:
JIMD Reports, Vol 60, Iss 1, Pp 96-104 (2021)
Abstract Two siblings were diagnosed with adult metachromatic leukodystrophy (MLD) and treated with hematopoietic stem cell transplantation (HSCT). While the older sibling was symptomatic at the time of diagnosis, her younger brother was diagnosed an
Externí odkaz:
https://doaj.org/article/b196cde2a6604a158ceb93c111aa079e
Autor:
Puriya Daniel Würtz Yazdanfard, Grigoris Effraimidis, Christoffer Valdorff Madsen, Lars Holme Nielsen, Åse Krogh Rasmussen, Jørgen Holm Petersen, Søren Schwartz Sørensen, Lars Køber, Vitor Hugo Fraga de Abreu, Vibeke Andrée Larsen, Ulla Feldt-Rasmussen
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 31, Iss , Pp 100841- (2022)
Background: Fabry disease (FD) is a lysosomal storage disorder resulting in systemic accumulation of globotriaosylceramide (Gb3) causing multi-organ dysfunction. The audiologic involvement in FD has been neglected in previous studies; while not a let
Externí odkaz:
https://doaj.org/article/6cd6ac5f35b14734ab6a47899baa2717
Autor:
Thomas Urup, Linn Gillberg, Katja Kaastrup, Maya Jeje Schuang Lü, Signe Regner Michaelsen, Vibeke Andrée Larsen, Ib Jarle Christensen, Helle Broholm, Ulrik Lassen, Kirsten Grønbæk, Hans Skovgaard Poulsen
Publikováno v:
Molecular Oncology, Vol 14, Iss 5, Pp 964-973 (2020)
Patients with recurrent glioblastoma achieving response to bevacizumab combined with chemotherapy have clinical improvement and prolonged survival. High gene expression of angiotensinogen (AGT) is associated with a poor bevacizumab response. Because
Externí odkaz:
https://doaj.org/article/a869f372b7954f5c8bf9715dcc5ecaf3
Autor:
Marie N N Hellem, Tua Vinther-Jensen, Lasse Anderberg, Esben Budtz-Jørgensen, Lena E Hjermind, Vibeke Andrée Larsen, Jørgen E Nielsen, Ian Law
Publikováno v:
PLoS ONE, Vol 16, Iss 6, p e0252683 (2021)
BackgroundHuntington's disease (HD) is an inherited, progressive neurodegenerative disease that has no cure. Striatal atrophy and hypometabolism has been described in HD as far as 15 years before clinical onset and therefore structural and functional
Externí odkaz:
https://doaj.org/article/92c324f278e24176875b8adc52bf1c98
Autor:
Urszula Maria Ciochon, Julie Bolette Brix Bindslev, Christina Engel Hoei-Hansen, Thomas Clement Truelsen, Vibeke Andrée Larsen, Michael Bachmann Nielsen, Adam Espe Hansen
Publikováno v:
Diagnostics, Vol 12, Iss 6, p 1459 (2022)
Previous studies suggest that the most common cause of spontaneous intracerebral hemorrhage in children and adolescents is arteriovenous malformations (AVMs). However, an update containing recently published data on pediatric spontaneous intracranial
Externí odkaz:
https://doaj.org/article/2fcf728522254787ab593d5000b90534
Autor:
Alexander Malcolm Rykkje, Dana Li, Jane Skjøth-Rasmussen, Vibeke Andrée Larsen, Michael Bachmann Nielsen, Adam Espe Hansen, Jonathan Frederik Carlsen
Publikováno v:
Diagnostics, Vol 11, Iss 8, p 1344 (2021)
For the radiological assessment of resection of high-grade gliomas, a 72-h diagnostic window is recommended to limit surgically induced contrast enhancements. However, such enhancements may occur earlier than 72 h post-surgery. This systematic review
Externí odkaz:
https://doaj.org/article/f2b277b31a1e4642957782895855faea
Autor:
Moshgan Amiri, Patrick M Fisher, Federico Raimondo, Annette Sidaros, Melita Cacic Hribljan, Marwan H Othman, Ivan Zibrandtsen, Simon S Albrechtsen, Ove Bergdal, Adam Espe Hansen, Christian Hassager, Joan Lilja S Højgaard, Elisabeth Waldemar Jakobsen, Helene Ravnholt Jensen, Jacob Møller, Vardan Nersesjan, Miki Nikolic, Markus Harboe Olsen, Sigurdur Thor Sigurdsson, Jacobo D Sitt, Christine Sølling, Karen Lise Welling, Lisette M Willumsen, John Hauerberg, Vibeke Andrée Larsen, Martin Fabricius, Gitte Moos Knudsen, Jesper Kjaergaard, Kirsten Møller, Daniel Kondziella
Publikováno v:
Brain 146(1), 50-64 (2023). doi:10.1093/brain/awac335
Functional MRI (fMRI) and EEG may reveal residual consciousness in patients with disorders of consciousness (DoC), as reflected by a rapidly expanding literature on chronic DoC. However, acute DoC is rarely investigated, although identifying residual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7ff0142369cc9b7bb28d38fb013ec68
https://doi.org/10.1093/brain/awac335
https://doi.org/10.1093/brain/awac335