Kamphorst W - Search Results

1

Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.

Rosso SM, Kamphorst W, de Graaf B, Willemsen R, Ravid R, Niermeijer MF, Spillantini MG, Heutink P, van Swieten JC. Rosso SM, et al. Among authors: kamphorst w. Brain. 2001 Oct;124(Pt 10):1948-57. doi: 10.1093/brain/124.10.1948. Brain. 2001. PMID: 11571213 Free article.

2

Complex compulsive behaviour in the temporal variant of frontotemporal dementia.

Rosso SM, Roks G, Stevens M, de Koning I, Tanghe HLJ, Kamphorst W, Ravid R, Niermeijer MF, van Swieten JC. Rosso SM, et al. Among authors: kamphorst w. J Neurol. 2001 Nov;248(11):965-70. doi: 10.1007/s004150170049. J Neurol. 2001. PMID: 11757960

3

Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathology.

Bronner IF, ter Meulen BC, Azmani A, Severijnen LA, Willemsen R, Kamphorst W, Ravid R, Heutink P, van Swieten JC. Bronner IF, et al. Among authors: kamphorst w. Brain. 2005 Nov;128(Pt 11):2645-53. doi: 10.1093/brain/awh591. Epub 2005 Jul 13. Brain. 2005. PMID: 16014652

4

Distinct genetic forms of frontotemporal dementia.

Seelaar H, Kamphorst W, Rosso SM, Azmani A, Masdjedi R, de Koning I, Maat-Kievit JA, Anar B, Donker Kaat L, Breedveld GJ, Dooijes D, Rozemuller JM, Bronner IF, Rizzu P, van Swieten JC. Seelaar H, et al. Among authors: kamphorst w. Neurology. 2008 Oct 14;71(16):1220-6. doi: 10.1212/01.wnl.0000319702.37497.72. Epub 2008 Aug 13. Neurology. 2008. PMID: 18703462

5

Familial aggregation of parkinsonism in progressive supranuclear palsy.

Donker Kaat L, Boon AJ, Azmani A, Kamphorst W, Breteler MM, Anar B, Heutink P, van Swieten JC. Donker Kaat L, et al. Among authors: kamphorst w. Neurology. 2009 Jul 14;73(2):98-105. doi: 10.1212/WNL.0b013e3181a92bcc. Epub 2009 May 20. Neurology. 2009. PMID: 19458322

6

Pathologic findings in a case of primary progressive aphasia.

Scheltens P, Ravid R, Kamphorst W. Scheltens P, et al. Among authors: kamphorst w. Neurology. 1994 Feb;44(2):279-82. doi: 10.1212/wnl.44.2.279. Neurology. 1994. PMID: 8309574

7

Familial aggregation in frontotemporal dementia.

Stevens M, van Duijn CM, Kamphorst W, de Knijff P, Heutink P, van Gool WA, Scheltens P, Ravid R, Oostra BA, Niermeijer MF, van Swieten JC. Stevens M, et al. Among authors: kamphorst w. Neurology. 1998 Jun;50(6):1541-5. doi: 10.1212/wnl.50.6.1541. Neurology. 1998. PMID: 9633692

8

Phenotypic variation in hereditary frontotemporal dementia with tau mutations.

van Swieten JC, Stevens M, Rosso SM, Rizzu P, Joosse M, de Koning I, Kamphorst W, Ravid R, Spillantini MG, Niermeijer, Heutink P. van Swieten JC, et al. Among authors: kamphorst w. Ann Neurol. 1999 Oct;46(4):617-26. doi: 10.1002/1531-8249(199910)46:4<617::aid-ana10>3.0.co;2-i. Ann Neurol. 1999. PMID: 10514099

9

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. Among authors: kamphorst w. Hum Mol Genet. 2000 Dec 12;9(20):3075-82. doi: 10.1093/hmg/9.20.3075. Hum Mol Genet. 2000. PMID: 11115852

10

Coexistent tau and amyloid pathology in hereditary frontotemporal dementia with tau mutations.

Rosso SM, Kamphorst W, Ravid R, van Swieten JC. Rosso SM, et al. Among authors: kamphorst w. Ann N Y Acad Sci. 2000;920:115-9. doi: 10.1111/j.1749-6632.2000.tb06912.x. Ann N Y Acad Sci. 2000. PMID: 11193139

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

104 results

Search Page

Filters