Hasil Pencarian - Kjell Arne Arntzen

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  1. 1
    The prevalence of hereditary neuromuscular disorders in Northern Norway

    The prevalence of hereditary neuromuscular disorders in Northern Norway oleh Kai Ivar Müller, Marijke Van Ghelue, Irene Lund, Christoffer Jonsrud, Kjell Arne Arntzen

    Diterbitkan 2021-01-01
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  2. 2
    Joint Effect of Carotid Plaque and C‐Reactive Protein on First‐Ever Ischemic Stroke and Myocardial Infarction?

    Joint Effect of Carotid Plaque and C‐Reactive Protein on First‐Ever Ischemic Stroke and Myocardial Infarction? oleh Agnethe Eltoft, Kjell Arne Arntzen, Tom Wilsgaard, John‐Bjarne Hansen, Ellisiv B. Mathiesen, Stein Harald Johnsen

    Diterbitkan 2018-06-01
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  3. 3
    Exercise and physical activity for persons with Charcot-Marie-Tooth Disease

    Exercise and physical activity for persons with Charcot-Marie-Tooth Disease oleh Andreas Lahelle, Mari Ellefsen-Martinsen, Hanne Ludt Fossmo, Andreas Dybesland Rosenberger, Aristomo Andries, Kjell Arne Arntzen, Cecilie Thommessen, Christian Alexander Vedeler, Kristin Ørstavik

    Diterbitkan 2022-05-01
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  4. 4
    Novel mutations in the HADHB gene causing a mild phenotype of mitochondrial trifunctional protein (MTP) deficiency

    Novel mutations in the HADHB gene causing a mild phenotype of mitochondrial trifunctional protein (MTP) deficiency oleh Kristin Ørstavik, Kjell Arne Arntzen, Per Mathisen, Paul Hoff Backe, Trine Tangeraas, Magnhild Rasmussen, Erle Kristensen, Marijke Van Ghelue, Christoffer Jonsrud, Yngve Thomas Bliksrud

    Diterbitkan 2022-05-01
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  5. 5
    Impact of Venous Thromboembolism on the Formation and Progression of Carotid Atherosclerosis: The Tromsø Study

    Impact of Venous Thromboembolism on the Formation and Progression of Carotid Atherosclerosis: The Tromsø Study oleh Caroline Lind, Birgit Småbrekke, Ludvig Balteskard Rinde, Kristian Hindberg, Ellisiv Bøgeberg Mathiesen, Stein Harald Johnsen, Kjell Arne Arntzen, Inger Njølstad, Willem Lijfering, Sigrid Kufaas Brækkan, John-Bjarne Hansen

    Diterbitkan 2017-06-01
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  6. 6
    ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9

    ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9 oleh Marie F. Smeland, Conor McClenaghan, Helen I. Roessler, Sanne Savelberg, Geir Åsmund Myge Hansen, Helene Hjellnes, Kjell Arne Arntzen, Kai Ivar Müller, Andreas Rosenberger Dybesland, Theresa Harter, Monica Sala-Rabanal, Chris H. Emfinger, Yan Huang, Soma S. Singareddy, Jamie Gunn, David F. Wozniak, Attila Kovacs, Maarten Massink, Federico Tessadori, Sarah M. Kamel, Jeroen Bakkers, Maria S. Remedi, Marijke Van Ghelue, Colin G. Nichols, Gijs van Haaften

    Diterbitkan 2019-10-01
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