Rizzu P - Search Results

1

Genome-wide association study confirms extant PD risk loci among the Dutch.

Simón-Sánchez J, van Hilten JJ, van de Warrenburg B, Post B, Berendse HW, Arepalli S, Hernandez DG, de Bie RM, Velseboer D, Scheffer H, Bloem B, van Dijk KD, Rivadeneira F, Hofman A, Uitterlinden AG, Rizzu P, Bochdanovits Z, Singleton AB, Heutink P. Simón-Sánchez J, et al. Among authors: rizzu p. Eur J Hum Genet. 2011 Jun;19(6):655-61. doi: 10.1038/ejhg.2010.254. Epub 2011 Jan 19. Eur J Hum Genet. 2011. PMID: 21248740 Free PMC article.

2

Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch families.

Heutink P, Stevens M, Rizzu P, Bakker E, Kros JM, Tibben A, Niermeijer MF, van Duijn CM, Oostra BA, van Swieten JC. Heutink P, et al. Among authors: rizzu p. Ann Neurol. 1997 Feb;41(2):150-9. doi: 10.1002/ana.410410205. Ann Neurol. 1997. PMID: 9029063

3

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands.

Rizzu P, Van Swieten JC, Joosse M, Hasegawa M, Stevens M, Tibben A, Niermeijer MF, Hillebrand M, Ravid R, Oostra BA, Goedert M, van Duijn CM, Heutink P. Rizzu P, et al. Am J Hum Genet. 1999 Feb;64(2):414-21. doi: 10.1086/302256. Am J Hum Genet. 1999. PMID: 9973279 Free PMC article.

4

Mutation-dependent aggregation of tau protein and its selective depletion from the soluble fraction in brain of P301L FTDP-17 patients.

Rizzu P, Joosse M, Ravid R, Hoogeveen A, Kamphorst W, van Swieten JC, Willemsen R, Heutink P. Rizzu P, et al. Hum Mol Genet. 2000 Dec 12;9(20):3075-82. doi: 10.1093/hmg/9.20.3075. Hum Mol Genet. 2000. PMID: 11115852

5

A double RING-H2 domain in RNF32, a gene expressed during sperm formation.

van Baren MJ, van der Linde HC, Breedveld GJ, Baarends WM, Rizzu P, de Graaff E, Oostra BA, Heutink P. van Baren MJ, et al. Among authors: rizzu p. Biochem Biophys Res Commun. 2002 Mar 22;292(1):58-65. doi: 10.1006/bbrc.2002.6612. Biochem Biophys Res Commun. 2002. PMID: 11890671

6

The DJ-1L166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexes.

Macedo MG, Anar B, Bronner IF, Cannella M, Squitieri F, Bonifati V, Hoogeveen A, Heutink P, Rizzu P. Macedo MG, et al. Among authors: rizzu p. Hum Mol Genet. 2003 Nov 1;12(21):2807-16. doi: 10.1093/hmg/ddg304. Epub 2003 Sep 2. Hum Mol Genet. 2003. PMID: 12952867

7

DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism.

Bonifati V, Rizzu P, Squitieri F, Krieger E, Vanacore N, van Swieten JC, Brice A, van Duijn CM, Oostra B, Meco G, Heutink P. Bonifati V, et al. Among authors: rizzu p. Neurol Sci. 2003 Oct;24(3):159-60. doi: 10.1007/s10072-003-0108-0. Neurol Sci. 2003. PMID: 14598065

8

DJ-1 colocalizes with tau inclusions: a link between parkinsonism and dementia.

Rizzu P, Hinkle DA, Zhukareva V, Bonifati V, Severijnen LA, Martinez D, Ravid R, Kamphorst W, Eberwine JH, Lee VM, Trojanowski JQ, Heutink P. Rizzu P, et al. Ann Neurol. 2004 Jan;55(1):113-8. doi: 10.1002/ana.10782. Ann Neurol. 2004. PMID: 14705119

9

CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementia.

Rizzu P, van Mil SE, Anar B, Rosso SM, Donker Kaat L, Heutink P, van Swieten JC. Rizzu P, et al. Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):944-6. doi: 10.1002/ajmg.b.30410. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16941655

10

Progranulin mutations in Dutch familial frontotemporal lobar degeneration.

Bronner IF, Rizzu P, Seelaar H, van Mil SE, Anar B, Azmani A, Donker Kaat L, Rosso S, Heutink P, van Swieten JC. Bronner IF, et al. Among authors: rizzu p. Eur J Hum Genet. 2007 Mar;15(3):369-74. doi: 10.1038/sj.ejhg.5201772. Epub 2007 Jan 17. Eur J Hum Genet. 2007. PMID: 17228326

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