Bindoff LA - Search Results

1

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.

2

[Multiple sclerosis - a mitochondria-mediated disease?].

Varhaug KN, Vedeler CA, Tzoulis C, Bindoff LA. Varhaug KN, et al. Among authors: bindoff la. Tidsskr Nor Laegeforen. 2017 Feb 21;137(4):284-287. doi: 10.4045/tidsskr.16.0210. eCollection 2017 Feb. Tidsskr Nor Laegeforen. 2017. PMID: 28225235 Free article. Review. Norwegian.

3

Leukoencephalopathy with brainstem and spinal cord involvement caused by a novel mutation in the DARS2 gene.

Tzoulis C, Tran GT, Gjerde IO, Aasly J, Neckelmann G, Rydland J, Varga V, Wadel-Andersen P, Bindoff LA. Tzoulis C, et al. Among authors: bindoff la. J Neurol. 2012 Feb;259(2):292-6. doi: 10.1007/s00415-011-6176-9. Epub 2011 Jul 27. J Neurol. 2012. PMID: 21792730

4

Serial diffusion imaging in a case of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes.

Tzoulis C, Bindoff LA. Tzoulis C, et al. Among authors: bindoff la. Stroke. 2009 Feb;40(2):e15-7. doi: 10.1161/STROKEAHA.108.523118. Epub 2008 Dec 18. Stroke. 2009. PMID: 19095975

5

MRI characterisation of adult onset alpha-methylacyl-coA racemase deficiency diagnosed by exome sequencing.

Haugarvoll K, Johansson S, Tzoulis C, Haukanes BI, Bredrup C, Neckelmann G, Boman H, Knappskog PM, Bindoff LA. Haugarvoll K, et al. Among authors: bindoff la. Orphanet J Rare Dis. 2013 Jan 3;8:1. doi: 10.1186/1750-1172-8-1. Orphanet J Rare Dis. 2013. PMID: 23286897 Free PMC article.

6

Progressive striatal necrosis associated with anti-NMDA receptor antibodies.

Tzoulis C, Vedeler C, Haugen M, Storstein A, Tran GT, Gjerde IO, Biermann M, Schwarzlmüller T, Bindoff LA. Tzoulis C, et al. Among authors: bindoff la. BMC Neurol. 2013 May 31;13:55. doi: 10.1186/1471-2377-13-55. BMC Neurol. 2013. PMID: 23725534 Free PMC article.

7

Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromes.

Tzoulis C, Neckelmann G, Mørk SJ, Engelsen BE, Viscomi C, Moen G, Ersland L, Zeviani M, Bindoff LA. Tzoulis C, et al. Among authors: bindoff la. Brain. 2010 May;133(Pt 5):1428-37. doi: 10.1093/brain/awq067. Epub 2010 Apr 16. Brain. 2010. PMID: 20400524

8

Acute mitochondrial encephalopathy reflects neuronal energy failure irrespective of which genome the genetic defect affects.

Tzoulis C, Bindoff LA. Tzoulis C, et al. Among authors: bindoff la. Brain. 2012 Dec;135(Pt 12):3627-34. doi: 10.1093/brain/aws223. Epub 2012 Oct 12. Brain. 2012. PMID: 23065482

9

Severe nigrostriatal degeneration without clinical parkinsonism in patients with polymerase gamma mutations.

Tzoulis C, Tran GT, Schwarzlmüller T, Specht K, Haugarvoll K, Balafkan N, Lilleng PK, Miletic H, Biermann M, Bindoff LA. Tzoulis C, et al. Among authors: bindoff la. Brain. 2013 Aug;136(Pt 8):2393-404. doi: 10.1093/brain/awt103. Epub 2013 Apr 26. Brain. 2013. PMID: 23625061

10

Novel SACS mutations identified by whole exome sequencing in a norwegian family with autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Tzoulis C, Johansson S, Haukanes BI, Boman H, Knappskog PM, Bindoff LA. Tzoulis C, et al. Among authors: bindoff la. PLoS One. 2013 Jun 13;8(6):e66145. doi: 10.1371/journal.pone.0066145. Print 2013. PLoS One. 2013. PMID: 23785480 Free PMC article.

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