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Bård Kronen Krossnes
Researcher at Haukeland University Hospital
Publications - 19
Citations - 462
Bård Kronen Krossnes is an academic researcher from Haukeland University Hospital. The author has contributed to research in topics: Hyperthermia & Paraneoplastic cerebellar degeneration. The author has an hindex of 11, co-authored 19 publications receiving 410 citations. Previous affiliations of Bård Kronen Krossnes include University of Bergen.
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Journal ArticleDOI
CT and MR Imaging Features of Primary Central Nervous System Lymphoma in Norway, 1989-2003
TL;DR: White matter periventricular contrast-enhancing single or multiple focal lesions were typical of non-AIDS PCNSL, and no or disseminated lesions heightened the risk of delayed or postmortem diagnosis.
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Increasing incidence and continued dismal outcome of primary central nervous system lymphoma in Norway 1989-2003 : time trends in a 15-year national survey.
Ingfrid S. Haldorsen,Ingfrid S. Haldorsen,Bård Kronen Krossnes,Jan Harald Aarseth,David Scheie,Tom Børge Johannesen,Olav Mella,Ansgar Espeland,Ansgar Espeland +8 more
TL;DR: Analysis of time trends in the incidence, clinical features, histologic diagnosis, treatment, and outcome of nonacquired immunodeficiency syndrome (non‐AIDS) PCNSL in Norway from 1989 to 2003 found that it is increasing in some countries, whereas it is stable in others.
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Morphological and immunohistochemical characterization of paraneoplastic cerebellar degeneration associated with Yo antibodies
Anette Storstein,Anette Storstein,Bård Kronen Krossnes,Christian A. Vedeler,Christian A. Vedeler +4 more
TL;DR: Immunohistochemical studies of paraneoplastic cerebellar degeneration are rare, and the findings vary.
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Antibodies to CRMP3-4 associated with limbic encephalitis and thymoma.
Anette Knudsen,Anette Knudsen,Geir Bredholt,Geir Bredholt,Anette Storstein,Anette Storstein,Leif Oltedal,Svend Davanger,Bård Kronen Krossnes,Bård Kronen Krossnes,J. Honnorat,Christian A. Vedeler,Christian A. Vedeler +12 more
TL;DR: It is illustrated that CRMP3–4 antibodies can be associated with subacute limbic encephalitis and thymoma, which has previously been associated with CRMP5.
Journal ArticleDOI
Severe fascioscapulohumeral muscular dystrophy presenting with Coats’ disease and mental retardation
Laurence A. Bindoff,Nanette Mjellem,Kristian Sommerfelt,Bård Kronen Krossnes,Fiona Roberts,Jørgen Krohn,Randi Skarpaas Tranheim,Irene D. Haggerty +7 more
TL;DR: Two Norwegian children with fascioscapulohumeral muscular dystrophy in whom Coats' disease, deafness, mental retardation and possible epilepsy were the presenting features are described and Cryotherapy was successful in maintaining sight in the other affected eyes.