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Page 1
[Hereditary ataxias].
Tallaksen CM. Tallaksen CM. Tidsskr Nor Laegeforen. 2008 Sep 11;128(17):1977-80. Tidsskr Nor Laegeforen. 2008. PMID: 18787576 Free article. Review. Norwegian.
[A young woman with a weakening leg].
Holmøy T, Braaten Ø, Hovden IA, Tallaksen CM. Holmøy T, et al. Among authors: tallaksen cm. Tidsskr Nor Laegeforen. 2011 Mar 18;131(6):583-6. doi: 10.4045/tidsskr.09.1499. Tidsskr Nor Laegeforen. 2011. PMID: 21423311 Free article. Norwegian.
EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias.
Harbo HF, Finsterer J, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B, De Jonghe P, Lossos A, Lynch T, Mariotti C, Schöls L, Spinazzola A, Szolnoki Z, Tabrizi SJ, Tallaksen C, Zeviani M, Burgunder JM, Gasser T; EFNS. Harbo HF, et al. Eur J Neurol. 2009 Jul;16(7):777-85. doi: 10.1111/j.1468-1331.2009.02646.x. Epub 2009 May 12. Eur J Neurol. 2009. PMID: 19469830
[Myasthenia gravis - optimal treatment and accurate diagnosis].
Gilhus NE, Kerty E, Løseth S, Mygland Å, Tallaksen C. Gilhus NE, et al. Tidsskr Nor Laegeforen. 2016 Jul 5;136(12-13):1089-94. doi: 10.4045/tidsskr.15.1259. eCollection 2016 Jul. Tidsskr Nor Laegeforen. 2016. PMID: 27381787 Free article. Review. Norwegian.
Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia.
Iqbal Z, Rydning SL, Wedding IM, Koht J, Pihlstrøm L, Rengmark AH, Henriksen SP, Tallaksen CM, Toft M. Iqbal Z, et al. Among authors: tallaksen cm. PLoS One. 2017 Mar 31;12(3):e0174667. doi: 10.1371/journal.pone.0174667. eCollection 2017. PLoS One. 2017. PMID: 28362824 Free PMC article.
112 results