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Year Number of Results
2009 1
2010 2
2011 7
2012 2
2013 2
2014 2
2017 1
2018 1
2020 1
2024 0

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18 results

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Page 1
LRP10 variants in progressive supranuclear palsy.
Vergouw LJM, Melhem S, Donker Kaat L, Chiu WZ, Kuipers DJS, Breedveld G, Boon AJW, Wang LS, Naj AC, Mlynarksi E, Cantwell L, Quadri M, Ross OA, Dickson DW, Schellenberg GD, van Swieten JC, Bonifati V, de Jong FJ. Vergouw LJM, et al. Among authors: chiu wz. Neurobiol Aging. 2020 Oct;94:311.e5-311.e10. doi: 10.1016/j.neurobiolaging.2020.04.016. Epub 2020 Apr 30. Neurobiol Aging. 2020. PMID: 32527607 Free PMC article.
Multireceptor fingerprints in progressive supranuclear palsy.
Chiu WZ, Donker Kaat L, Boon AJW, Kamphorst W, Schleicher A, Zilles K, van Swieten JC, Palomero-Gallagher N. Chiu WZ, et al. Alzheimers Res Ther. 2017 Apr 17;9(1):28. doi: 10.1186/s13195-017-0259-5. Alzheimers Res Ther. 2017. PMID: 28412965 Free PMC article.
Recent advances in progressive supranuclear palsy: a review.
Kaat DL, Chiu WZ, Boon AJ, van Swieten JC. Kaat DL, et al. Among authors: chiu wz. Curr Alzheimer Res. 2011 May;8(3):295-302. doi: 10.2174/156720511795563809. Curr Alzheimer Res. 2011. PMID: 21222597 Review.
Serum neurofilament light chain in progressive supranuclear palsy.
Donker Kaat L, Meeter LH, Chiu WZ, Melhem S, Boon AJW, Blennow K, Zetterberg H, van Swieten JC. Donker Kaat L, et al. Among authors: chiu wz. Parkinsonism Relat Disord. 2018 Nov;56:98-101. doi: 10.1016/j.parkreldis.2018.06.018. Epub 2018 Jun 12. Parkinsonism Relat Disord. 2018. PMID: 29937097
PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology.
Wong TH, Chiu WZ, Breedveld GJ, Li KW, Verkerk AJ, Hondius D, Hukema RK, Seelaar H, Frick P, Severijnen LA, Lammers GJ, Lebbink JH, van Duinen SG, Kamphorst W, Rozemuller AJ; Netherlands Brain Bank; Bakker EB; International Parkinsonism Genetics Network; Neumann M, Willemsen R, Bonifati V, Smit AB, van Swieten J. Wong TH, et al. Among authors: chiu wz. Brain. 2014 May;137(Pt 5):1361-73. doi: 10.1093/brain/awu067. Epub 2014 Apr 9. Brain. 2014. PMID: 24722252
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
Höglinger GU, Melhem NM, Dickson DW, Sleiman PM, Wang LS, Klei L, Rademakers R, de Silva R, Litvan I, Riley DE, van Swieten JC, Heutink P, Wszolek ZK, Uitti RJ, Vandrovcova J, Hurtig HI, Gross RG, Maetzler W, Goldwurm S, Tolosa E, Borroni B, Pastor P; PSP Genetics Study Group; Cantwell LB, Han MR, Dillman A, van der Brug MP, Gibbs JR, Cookson MR, Hernandez DG, Singleton AB, Farrer MJ, Yu CE, Golbe LI, Revesz T, Hardy J, Lees AJ, Devlin B, Hakonarson H, Müller U, Schellenberg GD. Höglinger GU, et al. Nat Genet. 2011 Jun 19;43(7):699-705. doi: 10.1038/ng.859. Nat Genet. 2011. PMID: 21685912 Free PMC article.
Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation.
Dopper EG, Seelaar H, Chiu WZ, de Koning I, van Minkelen R, Baker MC, Rozemuller AJ, Rademakers R, van Swieten JC. Dopper EG, et al. Among authors: chiu wz. J Mol Neurosci. 2011 Nov;45(3):354-8. doi: 10.1007/s12031-011-9626-z. Epub 2011 Aug 24. J Mol Neurosci. 2011. PMID: 21863316 Free PMC article.
18 results