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Page 1
Low prevalence of known pathogenic mutations in dominant PD genes: A Swedish multicenter study.
Puschmann A, Jiménez-Ferrer I, Lundblad-Andersson E, Mårtensson E, Hansson O, Odin P, Widner H, Brolin K, Mzezewa R, Kristensen J, Soller M, Rödström EY, Ross OA, Toft M, Breedveld GJ, Bonifati V, Brodin L, Zettergren A, Sydow O, Linder J, Wirdefeldt K, Svenningsson P, Nissbrandt H, Belin AC, Forsgren L, Swanberg M. Puschmann A, et al. Among authors: nissbrandt h. Parkinsonism Relat Disord. 2019 Sep;66:158-165. doi: 10.1016/j.parkreldis.2019.07.032. Epub 2019 Jul 31. Parkinsonism Relat Disord. 2019. PMID: 31422003 Free article.
Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden.
Ran C, Brodin L, Forsgren L, Westerlund M, Ramezani M, Gellhaar S, Xiang F, Fardell C, Nissbrandt H, Söderkvist P, Puschmann A, Ygland E, Olson L, Willows T, Johansson A, Sydow O, Wirdefeldt K, Galter D, Svenningsson P, Belin AC. Ran C, et al. Among authors: nissbrandt h. Neurobiol Aging. 2016 Sep;45:212.e5-212.e11. doi: 10.1016/j.neurobiolaging.2016.04.022. Epub 2016 May 3. Neurobiol Aging. 2016. PMID: 27255555 Free PMC article.
Association of a polymorphism in the ABCB1 gene with Parkinson's disease.
Westerlund M, Belin AC, Anvret A, Håkansson A, Nissbrandt H, Lind C, Sydow O, Olson L, Galter D. Westerlund M, et al. Among authors: nissbrandt h. Parkinsonism Relat Disord. 2009 Jul;15(6):422-4. doi: 10.1016/j.parkreldis.2008.11.010. Epub 2009 Feb 3. Parkinsonism Relat Disord. 2009. PMID: 19196542
DJ-1 Mutations are Rare in a Swedish Parkinson Cohort.
Anvret A, Blackinton JG, Westerlund M, Ran C, Sydow O, Willows T, Håkansson A, Nissbrandt H, Belin AC. Anvret A, et al. Among authors: nissbrandt h. Open Neurol J. 2011 Mar 22;5:8-11. doi: 10.2174/1874205X01105010008. Open Neurol J. 2011. PMID: 21532868 Free PMC article.
Fine mapping and resequencing of the PARK16 locus in Parkinson's disease.
Pihlstrøm L, Rengmark A, Bjørnarå KA, Dizdar N, Fardell C, Forsgren L, Holmberg B, Larsen JP, Linder J, Nissbrandt H, Tysnes OB, Dietrichs E, Toft M. Pihlstrøm L, et al. Among authors: nissbrandt h. J Hum Genet. 2015 Jul;60(7):357-62. doi: 10.1038/jhg.2015.34. Epub 2015 Apr 9. J Hum Genet. 2015. PMID: 25855069
Glucocerebrosidase variant T369M is not a risk factor for Parkinson's disease in Sweden.
Ran C, Brodin L, Gellhaar S, Westerlund M, Fardell C, Nissbrandt H, Söderkvist P, Sydow O, Markaki I, Hertz E, Wirdefeldt K, Svenningsson P. Ran C, et al. Among authors: nissbrandt h. Neurosci Lett. 2022 Jul 27;784:136767. doi: 10.1016/j.neulet.2022.136767. Epub 2022 Jun 30. Neurosci Lett. 2022. PMID: 35779693 Free article.
Cyclooxygenase-2 polymorphisms in Parkinson's disease.
Håkansson A, Bergman O, Chrapkowska C, Westberg L, Belin AC, Sydow O, Johnels B, Olson L, Holmberg B, Nissbrandt H. Håkansson A, et al. Among authors: nissbrandt h. Am J Med Genet B Neuropsychiatr Genet. 2007 Apr 5;144B(3):367-9. doi: 10.1002/ajmg.b.30449. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17171651
90 results