Dermaut B - Search Results

1

Novel APP mutation V715A associated with presenile Alzheimer's disease in a German family.

Cruts M, Dermaut B, Rademakers R, Van den Broeck M, Stögbauer F, Van Broeckhoven C. Cruts M, et al. Among authors: dermaut b. J Neurol. 2003 Nov;250(11):1374-5. doi: 10.1007/s00415-003-0182-5. J Neurol. 2003. PMID: 14648157 No abstract available.

2

PRNP Val129 homozygosity increases risk for early-onset Alzheimer's disease.

Dermaut B, Croes EA, Rademakers R, Van den Broeck M, Cruts M, Hofman A, van Duijn CM, Van Broeckhoven C. Dermaut B, et al. Ann Neurol. 2003 Mar;53(3):409-12. doi: 10.1002/ana.10507. Ann Neurol. 2003. PMID: 12601712

3

A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques.

Dermaut B, Kumar-Singh S, Engelborghs S, Theuns J, Rademakers R, Saerens J, Pickut BA, Peeters K, van den Broeck M, Vennekens K, Claes S, Cruts M, Cras P, Martin JJ, Van Broeckhoven C, De Deyn PP. Dermaut B, et al. Ann Neurol. 2004 May;55(5):617-26. doi: 10.1002/ana.20083. Ann Neurol. 2004. PMID: 15122701

4

A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.

van der Zee J, Rademakers R, Engelborghs S, Gijselinck I, Bogaerts V, Vandenberghe R, Santens P, Caekebeke J, De Pooter T, Peeters K, Lübke U, Van den Broeck M, Martin JJ, Cruts M, De Deyn PP, Van Broeckhoven C, Dermaut B. van der Zee J, et al. Among authors: dermaut b. Brain. 2006 Apr;129(Pt 4):841-52. doi: 10.1093/brain/awl029. Epub 2006 Feb 22. Brain. 2006. PMID: 16495329

5

Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family.

Brouwers N, Nuytemans K, van der Zee J, Gijselinck I, Engelborghs S, Theuns J, Kumar-Singh S, Pickut BA, Pals P, Dermaut B, Bogaerts V, De Pooter T, Serneels S, Van den Broeck M, Cuijt I, Mattheijssens M, Peeters K, Sciot R, Martin JJ, Cras P, Santens P, Vandenberghe R, De Deyn PP, Cruts M, Van Broeckhoven C, Sleegers K. Brouwers N, et al. Among authors: dermaut b. Arch Neurol. 2007 Oct;64(10):1436-46. doi: 10.1001/archneur.64.10.1436. Arch Neurol. 2007. PMID: 17923627

6

The cystatin C polymorphism is not associated with early onset Alzheimer's disease.

Roks G, Cruts M, Slooter AJ, Dermaut B, Hofman A, Van Broeckhoven C, Van Duijn CM. Roks G, et al. Among authors: dermaut b. Neurology. 2001 Jul 24;57(2):366-7. doi: 10.1212/wnl.57.2.366-a. Neurology. 2001. PMID: 11468337 No abstract available.

7

Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation.

Dermaut B, Kumar-Singh S, De Jonghe C, Cruts M, Löfgren A, Lübke U, Cras P, Dom R, De Deyn PP, Martin JJ, Van Broeckhoven C. Dermaut B, et al. Brain. 2001 Dec;124(Pt 12):2383-92. doi: 10.1093/brain/124.12.2383. Brain. 2001. PMID: 11701593

8

Variable expression of presenilin 1 is not a major determinant of risk for late-onset Alzheimer's disease.

Dermaut B, Roks G, Theuns J, Rademakers R, Houwing-Duistermaat JJ, Serneels S, Hofman A, Breteler MM, Cruts M, Van Broeckhoven C, van Duijn CM. Dermaut B, et al. J Neurol. 2001 Nov;248(11):935-9. doi: 10.1007/s004150170044. J Neurol. 2001. PMID: 11757955

9

Possible association of nicastrin polymorphisms and Alzheimer disease in the Finnish population.

Helisalmi S, Dermaut B, Hiltunen M, Mannermaa A, Van den Broeck M, Lehtovirta M, Koivisto AM, Iivonen S, Cruts M, Soininen H, Van Broeckhoven C. Helisalmi S, et al. Among authors: dermaut b. Neurology. 2004 Jul 13;63(1):173-5. doi: 10.1212/01.wnl.0000133153.98139.4e. Neurology. 2004. PMID: 15249634

10

Early cognitive decline is associated with prion protein codon 129 polymorphism.

Croes EA, Dermaut B, Houwing-Duistermaat JJ, Van den Broeck M, Cruts M, Breteler MM, Hofman A, van Broeckhoven C, van Duijn CM. Croes EA, et al. Among authors: dermaut b. Ann Neurol. 2003 Aug;54(2):275-6. doi: 10.1002/ana.10658. Ann Neurol. 2003. PMID: 12891686 No abstract available.

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