Haugarvoll K - Search Results

1

Meta-analysis of whole-exome sequencing data from two independent cohorts finds no evidence for rare variant enrichment in Parkinson disease associated loci.

Gaare JJ, Nido G, Dölle C, Sztromwasser P, Alves G, Tysnes OB, Haugarvoll K, Tzoulis C. Gaare JJ, et al. Among authors: haugarvoll k. PLoS One. 2020 Oct 1;15(10):e0239824. doi: 10.1371/journal.pone.0239824. eCollection 2020. PLoS One. 2020. PMID: 33002040 Free PMC article.

2

Differential effect of environmental risk factors on postural instability gait difficulties and tremor dominant Parkinson's disease.

Skeie GO, Muller B, Haugarvoll K, Larsen JP, Tysnes OB. Skeie GO, et al. Among authors: haugarvoll k. Mov Disord. 2010 Sep 15;25(12):1847-52. doi: 10.1002/mds.23178. Mov Disord. 2010. PMID: 20669310

3

Parkinson disease: associated disorders in the Norwegian population based incident ParkWest study.

Skeie GO, Muller B, Haugarvoll K, Larsen JP, Tysnes OB. Skeie GO, et al. Among authors: haugarvoll k. Parkinsonism Relat Disord. 2013 Jan;19(1):53-5. doi: 10.1016/j.parkreldis.2012.07.003. Epub 2012 Jul 26. Parkinsonism Relat Disord. 2013. PMID: 22841686

4

Number of CAG repeats in POLG1 and its association with Parkinson disease in the Norwegian population.

Balafkan N, Tzoulis C, Müller B, Haugarvoll K, Tysnes OB, Larsen JP, Bindoff LA. Balafkan N, et al. Among authors: haugarvoll k. Mitochondrion. 2012 Nov;12(6):640-3. doi: 10.1016/j.mito.2012.08.004. Epub 2012 Aug 29. Mitochondrion. 2012. PMID: 22963882

5

Treatment in early Parkinson's disease: the Norwegian ParkWest study.

Tveiten OV, Skeie GO, Haugarvoll K, Müller B, Larsen JP, Tysnes OB. Tveiten OV, et al. Among authors: haugarvoll k. Acta Neurol Scand. 2013 Aug;128(2):107-13. doi: 10.1111/ane.12055. Epub 2012 Nov 29. Acta Neurol Scand. 2013. PMID: 23190324

6

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. 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.

7

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: haugarvoll k. Brain. 2013 Aug;136(Pt 8):2393-404. doi: 10.1093/brain/awt103. Epub 2013 Apr 26. Brain. 2013. PMID: 23625061

8

Myoclonus-dystonia and epilepsy in a family with a novel epsilon-sarcoglycan mutation.

Haugarvoll K, Tzoulis C, Tran GT, Karlsen B, Engelsen BA, Knappskog PM, Bindoff LA. Haugarvoll K, et al. J Neurol. 2014 Feb;261(2):358-62. doi: 10.1007/s00415-013-7203-9. Epub 2013 Dec 3. J Neurol. 2014. PMID: 24297365

9

HTRA2 p.G399S in Parkinson disease, essential tremor, and tremulous cervical dystonia.

Tzoulis C, Zayats T, Knappskog PM, Müller B, Larsen JP, Tysnes OB, Bindoff LA, Johansson S, Haugarvoll K. Tzoulis C, et al. Among authors: haugarvoll k. Proc Natl Acad Sci U S A. 2015 May 5;112(18):E2268. doi: 10.1073/pnas.1503105112. Epub 2015 Mar 30. Proc Natl Acad Sci U S A. 2015. PMID: 25825781 Free PMC article. No abstract available.

10

A woman in her 70s with chronic walking difficulties.

Flønes IH, Haugarvoll K, Sundal C, Tzoulis C. Flønes IH, et al. Among authors: haugarvoll k. Tidsskr Nor Laegeforen. 2015 Oct 20;135(19):1753-5. doi: 10.4045/tidsskr.15.0111. eCollection 2015 Oct 20. Tidsskr Nor Laegeforen. 2015. PMID: 26486671 Free article. English, Norwegian. No abstract available.

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