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Page 1
The genetics of frontotemporal dementia.
Haugarvoll K, Wszolek ZK, Hutton M. Haugarvoll K, et al. Neurol Clin. 2007 Aug;25(3):697-715, vi. doi: 10.1016/j.ncl.2007.03.002. Neurol Clin. 2007. PMID: 17659186 Review.
ELAVL4, PARK10, and the Celts.
Haugarvoll K, Toft M, Ross OA, Stone JT, Heckman MG, White LR, Lynch T, Gibson JM, Wszolek ZK, Uitti RJ, Aasly JO, Farrer MJ. Haugarvoll K, et al. Mov Disord. 2007 Mar 15;22(4):585-7. doi: 10.1002/mds.21336. Mov Disord. 2007. PMID: 17230446
Lack of evidence for association of Parkin promoter polymorphism (PRKN-258) with increased risk of Parkinson's disease.
Ross OA, Haugarvoll K, Stone JT, Heckman MG, White LR, Aasly JO, Mark Gibson J, Lynch T, Wszolek ZK, Uitti RJ, Farrer MJ. Ross OA, et al. Among authors: haugarvoll k. Parkinsonism Relat Disord. 2007 Oct;13(7):386-8. doi: 10.1016/j.parkreldis.2007.01.010. Epub 2007 Apr 2. Parkinsonism Relat Disord. 2007. PMID: 17400506 Free PMC article.
Dopamine beta-hydroxylase -1021C>T association and Parkinson's disease.
Ross OA, Heckman MG, Soto AI, Diehl NN, Haugarvoll K, Vilariño-Güell C, Aasly JO, Sando S, Gibson JM, Lynch T, Krygowska-Wajs A, Opala G, Barcikowska M, Czyzewski K, Uitti RJ, Wszolek ZK, Farrer MJ. Ross OA, et al. Among authors: haugarvoll k. Parkinsonism Relat Disord. 2008 Nov;14(7):544-7. doi: 10.1016/j.parkreldis.2008.07.002. Epub 2008 Aug 22. Parkinsonism Relat Disord. 2008. PMID: 18722802 Free PMC article.
Fine-mapping and candidate gene investigation within the PARK10 locus.
Haugarvoll K, Toft M, Skipper L, Heckman MG, Crook JE, Soto A, Ross OA, Hulihan MM, Kachergus JM, Sando SB, White LR, Lynch T, Gibson JM, Uitti RJ, Wszolek ZK, Aasly JO, Farrer MJ. Haugarvoll K, et al. Eur J Hum Genet. 2009 Mar;17(3):336-43. doi: 10.1038/ejhg.2008.187. Epub 2008 Oct 15. Eur J Hum Genet. 2009. PMID: 18854859 Free PMC article.
FGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expression.
Wider C, Dachsel JC, Soto AI, Heckman MG, Diehl NN, Yue M, Lincoln S, Aasly JO, Haugarvoll K, Trojanowski JQ, Papapetropoulos S, Mash D, Rajput A, Rajput AH, Gibson JM, Lynch T, Dickson DW, Uitti RJ, Wszolek ZK, Farrer MJ, Ross OA. Wider C, et al. Among authors: haugarvoll k. Mov Disord. 2009 Feb 15;24(3):455-9. doi: 10.1002/mds.22442. Mov Disord. 2009. PMID: 19133659 Free PMC article.
Phactr2 and Parkinson's disease.
Wider C, Lincoln SJ, Heckman MG, Diehl NN, Stone JT, Haugarvoll K, Aasly JO, Gibson JM, Lynch T, Rajput A, Rajput ML, Uitti RJ, Wszolek ZK, Farrer MJ, Ross OA. Wider C, et al. Among authors: haugarvoll k. Neurosci Lett. 2009 Mar 27;453(1):9-11. doi: 10.1016/j.neulet.2009.02.009. Epub 2009 Feb 10. Neurosci Lett. 2009. PMID: 19429005 Free PMC article.
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.
Haugarvoll K, Rademakers R, Kachergus JM, Nuytemans K, Ross OA, Gibson JM, Tan EK, Gaig C, Tolosa E, Goldwurm S, Guidi M, Riboldazzi G, Brown L, Walter U, Benecke R, Berg D, Gasser T, Theuns J, Pals P, Cras P, De Deyn PP, Engelborghs S, Pickut B, Uitti RJ, Foroud T, Nichols WC, Hagenah J, Klein C, Samii A, Zabetian CP, Bonifati V, Van Broeckhoven C, Farrer MJ, Wszolek ZK. Haugarvoll K, et al. Neurology. 2008 Apr 15;70(16 Pt 2):1456-60. doi: 10.1212/01.wnl.0000304044.22253.03. Epub 2008 Mar 12. Neurology. 2008. PMID: 18337586 Free PMC article.
PARK8 LRRK2 parkinsonism.
Haugarvoll K, Wszolek ZK. Haugarvoll K, et al. Curr Neurol Neurosci Rep. 2006 Jul;6(4):287-94. doi: 10.1007/s11910-006-0020-0. Curr Neurol Neurosci Rep. 2006. PMID: 16822348 Review.
Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosis.
Sundal C, Baker M, Karrenbauer V, Gustavsen M, Bedri S, Glaser A, Myhr KM, Haugarvoll K, Zetterberg H, Harbo H, Kockum I, Hillert J, Wszolek Z, Rademakers R, Andersen O. Sundal C, et al. Among authors: haugarvoll k. Eur J Neurol. 2015 Feb;22(2):328-333. doi: 10.1111/ene.12572. Epub 2014 Oct 13. Eur J Neurol. 2015. PMID: 25311247 Free PMC article.
59 results