Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Jana Rydland"'
Publikováno v:
Case Reports in Neurology, Vol 5, Iss 3, Pp 149-154 (2013)
Background: Progressive multifocal leukoencephalopathy (PML) is a rapidly progressive, potentially fatal, demyelinating disease affecting immunosuppressed patients. PML is rarely reported in cases with no underlying disease or immunosuppression-assoc
Externí odkaz:
https://doaj.org/article/e4b220f128254412af9b14393d954559
Autor:
Asta Kristine Håberg, Tommy Arild Hammer, Kjell Arne Kvistad, Jana Rydland, Tomm B Müller, Live Eikenes, Mari Gårseth, Lars Jacob Stovner
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0151080 (2016)
Evaluate types and prevalence of all, incidental, and clinically relevant incidental intracranial findings, i.e. those referred to primary physician or clinical specialist, in a cohort between 50 and 66 years from the Nord-Trøndelag Health (HUNT) st
Externí odkaz:
https://doaj.org/article/e230b631b49a4adfba516ad696726ad7
Autor:
Hrvoje Miletic, Terje Nordberg, Snezana Maric, Tom Børge Johannesen, Jana Rydland, Tor Åge Myklebust, Bernt J. Due-Tønnessen, Kristin Smistad Myrmel, Ole Solheim, Anne Grete Bechensteen, Finn Wesenberg, Tore Stokland, Johan Cappelen, Ingrid Torsvik, Paulina Due-Tønnessen, Bård Krossnes, Viggo Moholdt, Tryggve Lundar, Gry Wikran, Bernward Zeller, Petter Brandal, Aleksandra Kepka, Kristin Solem, Einar Stensvold
Publikováno v:
66:e27910
Pediatric Blood & Cancer
Pediatric Blood & Cancer
Background: A previous study based on Norwegian Cancer Registry data suggested regional differences in overall survival (OS) after treatment for medulloblastoma (MB) and supratentorial primitive neuroectodermal tumor (CNS-PNET) in Norway. The purpose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9f9f699f15b1e73cf5f46dd4d573f3b
http://hdl.handle.net/10852/76067
http://hdl.handle.net/10852/76067
Publikováno v:
Case Reports in Neurology
Case Reports in Neurology, Vol 5, Iss 3, Pp 149-154 (2013)
Case Reports in Neurology, Vol 5, Iss 3, Pp 149-154 (2013)
Background: Progressive multifocal leukoencephalopathy (PML) is a rapidly progressive, potentially fatal, demyelinating disease affecting immunosuppressed patients. PML is rarely reported in cases with no underlying disease or immunosuppression-assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b1723ae25a3e3fbadf629d58a4c6932
http://europepmc.org/articles/PMC3806704
http://europepmc.org/articles/PMC3806704
Autor:
Marie Søfteland Sandvei, Kjell Arne Kvistad, Lars Jacob Stovner, Jana Rydland, Tomm B. Müller, Mari Gårseth, Anne Vik, Asta Håberg
Publikováno v:
Neurosurgery. 73:256-261
Background Rupture risk of unruptured intracranial aneurysms (UIAs) has been investigated in studies observing the natural history of this condition. Such studies have been prone to selection bias that may influence the results. Objective To calculat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e7ab74fe38efd54ca26b6cd432bb174
https://doi.org/10.1227/01.neu.0000430295.23799.16
https://doi.org/10.1227/01.neu.0000430295.23799.16
Autor:
Geoffrey T. Manley, Kjell Arne Kvistad, Veronika Brezova, Toril Skandsen, Anne Vik, Mari Folvik, Kent Gøran Moen, Jana Rydland
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 83:1193-1200
To study the evolution of traumatic axonal injury (TAI) detected by structural MRI in patients with moderate and severe traumatic brain injury (TBI) during the first year and relate findings to outcome.58 patients with TBI (Glasgow Coma Scale score 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0de4237df24f44a0176c4875fa4c6a9
https://doi.org/10.1136/jnnp-2012-302644
https://doi.org/10.1136/jnnp-2012-302644
Autor:
Jana Rydland, Charalampos Tzoulis, Viktoria Varga, Laurence A. Bindoff, Jan O. Aasly, Pia Wadel-Andersen, Ivar Otto Gjerde, Gesche Neckelmann, Gia T. Tran
Publikováno v:
Journal of Neurology. 259:292-296
Leukoencephalopathy with brainstem and spinal cord involvement and elevated lactate (LBSL) is a rare, autosomal recessive disorder caused by mutations in the gene encoding a mitochondrial aspartyl-tRNA synthetase, DARS2. The disease is characterized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c185c54e1dba57c84647c9bcdf332f7
https://doi.org/10.1007/s00415-011-6176-9
https://doi.org/10.1007/s00415-011-6176-9
Autor:
Lars Jacob Stovner, Mari Gårseth, Jana Rydland, Kjell Arne Kvistad, Live Eikenes, Asta Håberg, Tomm B. Müller, Tommy Arild Hammer
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0151080 (2016)
PLoS ONE
PLoS ONE
Objectives Evaluate types and prevalence of all, incidental, and clinically relevant incidental intracranial findings, i.e. those referred to primary physician or clinical specialist, in a cohort between 50 and 66 years from the Nord-Trøndelag Healt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c822f5b3746f16508cbb31cff5b162b8
http://hdl.handle.net/11250/2395820
http://hdl.handle.net/11250/2395820
Publikováno v:
Archives of disease in childhood. Fetal and neonatal edition. 100(6)
A non-dysmorphic term boy presented with inspiratory stridor shortly following delivery. Following clinical examination and thoracic x-ray, no external features or other clinical findings revealed any obvious explanation. Laryngomalacia was suspected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d47acc95f86da4fc14767149748722b5
https://pubmed.ncbi.nlm.nih.gov/26126847
https://pubmed.ncbi.nlm.nih.gov/26126847