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[Mitochondrial disease caused by the m.3243A>G mutation].
Varhaug KN, Hikmat O, Bindoff LA. Varhaug KN, et al. Among authors: bindoff la. Tidsskr Nor Laegeforen. 2022 Jun 27;142(10). doi: 10.4045/tidsskr.21.0729. Print 2022 Jun 28. Tidsskr Nor Laegeforen. 2022. PMID: 35763848 Free article. Review. Norwegian.
[The genetic basis of muscle disease].
Bindoff L, Gilhus NE. Bindoff L, et al. Tidsskr Nor Laegeforen. 2003 Sep 25;123(18):2588-92. Tidsskr Nor Laegeforen. 2003. PMID: 14714051 Review. Norwegian.
[A man with progressive spastic paraparesis].
Sanaker PS, Lindland S, Rekeland F, Bindoff LA. Sanaker PS, et al. Among authors: bindoff la. Tidsskr Nor Laegeforen. 2007 Nov 29;127(23):3085-7. Tidsskr Nor Laegeforen. 2007. PMID: 18098376 Norwegian.
[When the most common isn't the explanation].
Bindoff LA. Bindoff LA. Tidsskr Nor Laegeforen. 2011 Mar 18;131(6):586. doi: 10.4045/tidsskr.11.0015. Tidsskr Nor Laegeforen. 2011. PMID: 21423312 Free article. Norwegian. No abstract available.
A man in his 50s with high ferritin levels and increasing cognitive impairment.
Bjørk MH, Gjerde IO, Tzoulis C, Ulvik RJ, Bindoff LA. Bjørk MH, et al. Among authors: bindoff la. Tidsskr Nor Laegeforen. 2015 Aug 25;135(15):1369-72. doi: 10.4045/tidsskr.14.1115. eCollection 2015 Aug 25. Tidsskr Nor Laegeforen. 2015. PMID: 26315240 Free article. English, Norwegian. No abstract available.
ADCK3 mutations with epilepsy, stroke-like episodes and ataxia: a POLG mimic?
Hikmat O, Tzoulis C, Knappskog PM, Johansson S, Boman H, Sztromwasser P, Lien E, Brodtkorb E, Ghezzi D, Bindoff LA. Hikmat O, et al. Among authors: bindoff la. Eur J Neurol. 2016 Jul;23(7):1188-94. doi: 10.1111/ene.13003. Epub 2016 Apr 23. Eur J Neurol. 2016. PMID: 27106809
226 results