Hereditary ataxias, epidemiological and genetic studies in a Norwegian population
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- Institutt for klinisk medisin [10814]
Abstract
No abstract.List of papers
Paper I Erichsen AK, Koht J, Stray-Pedersen A, Abdelnoor M, Tallaksen CM. Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study Brain. 2009 Jun;132(Pt 6):1577-88. The paper is removed from the thesis in DUO due to publisher restrictions. The published version is available at: https://doi.org/10.1093/brain/awp056 |
Paper II Koht J, Bjørnarå KA, Jørum E, Tallaksen CM. Ataxia with vitamin E deficiency in southeast Norway, case report Acta Neurol Scand Suppl. 2009;(189):42-5. The paper is removed from the thesis in DUO due to publisher restrictions. The published version is available at: https://doi.org/10.1111/j.1600-0404.2009.01214.x |
Paper III Koht J, Stevanin G, Durr A, Mundwiller E, Brice A, Tallaksen CM. SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG gene Acta Neurol Scand. 2012 Feb;125(2):116-22. The paper is removed from the thesis in DUO due to publisher restrictions. The published version is available at: https://doi.org/10.1111/j.1600-0404.2011.01504.x |
Paper IV Koht J, Tallaksen CM, Mundwiller E, Gaussen M, Tesson C, Brice A, Durr A, Stevanin G. A late onset autosomal dominant ataxia maps to chromosome 10q26.3. The paper is removed from the thesis in DUO due to publisher restrictions. |