Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Espen, Lien"'
Autor:
Anne Elisabeth Brandt, Torstein B. Rø, Torun G. Finnanger, Ruth E. Hypher, Espen Lien, Bendik Lund, Cathy Catroppa, Stein Andersson, Kari Risnes, Jan Stubberud
Publikováno v:
Frontiers in Neurology, Vol 14 (2024)
BackgroundPediatric acquired brain injury (pABI) profoundly affects cognitive functions, encompassing IQ and executive functions (EFs). Particularly, young age at insult may lead to persistent and debilitating deficits, affecting daily-life functioni
Externí odkaz:
https://doaj.org/article/9bdde7067c97483db268f50ef99d2f9c
Autor:
Mari Olsen, Anne Vik, Espen Lien, Kari Schirmer-Mikalsen, Oddrun Fredriksli, Turid Follestad, Oddrun Sandrød, Torun G. Finnanger, Toril Skandsen
Publikováno v:
Journal of neurosurgery. Pediatrics. 29(4)
OBJECTIVE The primary aim of this study was to evaluate the global outcome longitudinally over 5 years in children and adolescents surviving moderate to severe traumatic brain injury (msTBI) to investigate changes in outcome over time. The secondary
Autor:
Jasmina Majkic Tajsic, Espen Lien, Petra Aden, Magnhild Rasmussen, Nanette Mjellem, Ellen Johanne Annexstad
Publikováno v:
Tidsskrift for Den norske legeforening. 137:108-111
Children with muscular diseases constitute an important group in paediatric neurology. Some of the conditions are very serious and require extensive interdisciplinary treatment and facilitation. There is some degree of optimism regarding the possibil
Autor:
Tom Ivar Lund Nilsen, Torun Gangaune Finnanger, Kent Gøran Moen, Toril Skandsen, Oddvar Uleberg, Oddrun Fredriksli, Mari Olsen, Anne Vik, Espen Lien
Publikováno v:
European journal of paediatric neurology
Objective: In this study we wanted to estimate population-based rates of incidence and mortality of moderate and severe traumatic brain injury (TBI) in children in one specific region in Norway. Methods: In the region there are seven acute care hospi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6614223aca60e3e75203fc90126d60a5
https://hdl.handle.net/11250/2739870
https://hdl.handle.net/11250/2739870
Autor:
James A. Blackman, Rolv T. Lie, Espen Lien, Guro L. Andersen, Yongde Bao, Magne Stoknes, Torstein Vik
Publikováno v:
European Journal of Paediatric Neurology. 19:286-291
Objective To use case–parent triad data to investigate if cerebral palsy (CP) is associated with variants of the APOE gene, the rs59007384 SNP of the TOMM40 gene or combined haplotypes of the two genes. Study design DNA was analyzed in buccal swabs
Autor:
Guro L. Andersen, Heather Gordish-Dressman, Espen Lien, Yongde Bao, Torstein Vik, James A. Blackman, Jon Skranes
Publikováno v:
Acta Paediatrica. 104:701-706
Aim Apolipoprotein E (apoE) influences repair and other processes in the brain, and the apoE4 variant is a risk factor for Alzheimer's disease and for prolonged recovery following traumatic brain injury. We previously reported that specific single nu
Autor:
Petra, Aden, Ellen J, Annexstad, Espen, Lien, Jasmina Majkic, Tajsic, Nanette, Mjellem, Magnhild, Rasmussen
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 137(2)
Children with muscular diseases constitute an important group in paediatric neurology. Some of the conditions are very serious and require extensive interdisciplinary treatment and facilitation. There is some degree of optimism regarding the possibil
Autor:
Espen Lien, Guro L. Andersen, Heather Gordish-Dressman, Jon Skranes, Torstein Vik, Yongde Bao, James A. Blackman
Publikováno v:
European Journal of Paediatric Neurology. 18:591-596
The apoE protein is the most important lipid transporter in the brain and has also been shown to have several regulatory functions in the central nervous system. The production of apoE is regulated by a number of genes and increases under certain con
Publikováno v:
Annals of neurology. 80(2)
Autor:
Pawel Szymon Sztromwasser, Omar Hikmat, Eylert Brodtkorb, Stefan Johansson, Daniele Ghezzi, Espen Lien, Charalampos Tzoulis, Laurence A. Bindoff, Helge Boman, Per M. Knappskog
Publikováno v:
European Journal of Neurology
Background and purpose Defects of coenzyme Q10 (CoQ10) metabolism cause a variety of disorders ranging from isolated myopathy to multisystem involvement. ADCK3 is one of several genes associated with CoQ10 deficiency that presents with progressive ce