Van Broeckhoven C - Search Results

1

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. Among authors: van duijn cm, van broeckhoven c. J Neurol. 2001 Nov;248(11):935-9. doi: 10.1007/s004150170044. J Neurol. 2001. PMID: 11757955

2

Apolipoprotein E genotype and concomitant clinical features in early-onset Alzheimer's disease.

Bronzova J, van Duijn CM, Havekes LM, de Knijff P, Van Broeckhoven C, Hofman A. Bronzova J, et al. Among authors: van duijn cm, van broeckhoven c. J Neurol. 1996 Jun;243(6):465-8. doi: 10.1007/BF00900501. J Neurol. 1996. PMID: 8803820

3

Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease.

Cruts M, van Duijn CM, Backhovens H, Van den Broeck M, Wehnert A, Serneels S, Sherrington R, Hutton M, Hardy J, St George-Hyslop PH, Hofman A, Van Broeckhoven C. Cruts M, et al. Among authors: van duijn cm, van den broeck m, van broeckhoven c. Hum Mol Genet. 1998 Jan;7(1):43-51. doi: 10.1093/hmg/7.1.43. Hum Mol Genet. 1998. PMID: 9384602

4

Presenilin mutations in Alzheimer's disease.

Cruts M, Van Broeckhoven C. Cruts M, et al. Among authors: van broeckhoven c. Hum Mutat. 1998;11(3):183-90. doi: 10.1002/(SICI)1098-1004(1998)11:3<183::AID-HUMU1>3.0.CO;2-J. Hum Mutat. 1998. PMID: 9521418 Review.

5

Molecular genetics of Alzheimer's disease.

Cruts M, Van Broeckhoven C. Cruts M, et al. Among authors: van broeckhoven c. Ann Med. 1998 Dec;30(6):560-5. doi: 10.3109/07853899809002605. Ann Med. 1998. PMID: 9920359 Free article. Review.

6

Apolipoprotein E genotype and progression of Alzheimer's disease: the Rotterdam Study.

Slooter AJ, Houwing-Duistermaat JJ, van Harskamp F, Cruts M, Van Broeckhoven C, Breteler MM, Hofman A, Stijnen T, van Duijn CM. Slooter AJ, et al. Among authors: van duijn cm, van harskamp f, van broeckhoven c. J Neurol. 1999 Apr;246(4):304-8. doi: 10.1007/s004150050351. J Neurol. 1999. PMID: 10367700

7

Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertion.

Dermaut B, Cruts M, Backhovens H, Lübke U, Van Everbroeck B, Sciot R, Dom R, Martin JJ, Van Broeckhoven C, Cras P. Dermaut B, et al. Among authors: van everbroeck b, van broeckhoven c. J Neurol. 2000 May;247(5):364-8. doi: 10.1007/s004150050603. J Neurol. 2000. PMID: 10896268

8

The alpha2-macroglobulin gene in AD: a population-based study and meta-analysis.

Koster MN, Dermaut B, Cruts M, Houwing-Duistermaat JJ, Roks G, Tol J, Ott A, Hofman A, Munteanu G, Breteler MM, van Duijn CM, Van Broeckhoven C. Koster MN, et al. Among authors: van duijn cm, van broeckhoven c. Neurology. 2000 Sep 12;55(5):678-84. doi: 10.1212/wnl.55.5.678. Neurology. 2000. PMID: 10980733

9

Transcriptional regulation of Alzheimer's disease genes: implications for susceptibility.

Theuns J, Van Broeckhoven C. Theuns J, et al. Among authors: van broeckhoven c. Hum Mol Genet. 2000 Oct;9(16):2383-94. doi: 10.1093/hmg/9.16.2383. Hum Mol Genet. 2000. PMID: 11005793 Review.

10

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: van duijn cm, van broeckhoven c. Neurology. 2001 Jul 24;57(2):366-7. doi: 10.1212/wnl.57.2.366-a. Neurology. 2001. PMID: 11468337 No abstract available.

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