Hereditary spinocerebellar degenerative disorders in Norway. Molecular and clinical studies of ataxia subtypes in a Norwegian patient population
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- Institutt for klinisk medisin [10751]
Abstract
No abstract.List of papers
Paper I Wedding IM, Koht J, Dietrichs E, Landro NI, Tallaksen CME. “Cognition is only minimally impaired in Spinocerebellar ataxia type 14 (SCA14): a neuropsychological study of ten Norwegian subjects compared to intrafamilial controls and population norm.” BMC Neurol. 2013 Nov 29;13:186. The paper is available in DUO: http://urn.nb.no/URN:NBN:no-40243 |
Paper II Wedding IM, Kroken M, Henriksen SP, Selmer KK, Fiskerstrand T, Knappskog PM, Berge T, Tallaksen CME. “Friedreich ataxia in Norway – an epidemiological, molecular and clinical study.” Orphanet J Rare Dis. 2015 Sep 4;10:108. The paper is available in DUO: http://urn.nb.no/URN:NBN:no-51405 |
Paper III Wedding IM, Koht J, Tran GT, Misceo D, Selmer KK, Holmgren A, Frengen E, Bindoff L, Tallaksen CME, Tzoulis C. “Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions.” PLoS One. 2014 Jan 22;9(1):e86340. doi: 10.1371 The paper is available in DUO: http://urn.nb.no/URN:NBN:no-41162 |
Paper IV Rydning, SL, Wedding IM, Koht J, Chawla M, Oye AM, Sheng Y, Vigeland MD, Selmer KK, Tallaksen CME. “A founder mutation p.H701P identified as a major cause of SPG7 in Norway.” Accepted version available in DUO: http://urn.nb.no/URN:NBN:no-53845 |