Dermaut B - Search Results

1

The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease.

Theuns J, Feuk L, Dermaut B, Del-Favero J, Roks G, Van den Bossche D, Corsmit E, Van den Broeck M, van Duijn CM, Cruts M, Brookes AJ, Van Broeckhoven C. Theuns J, et al. Among authors: dermaut b. Hum Genet. 2001 Jun;108(6):552-3. doi: 10.1007/s004390100508. Hum Genet. 2001. PMID: 11499683 No abstract available.

2

The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer disease.

Dermaut B, Cruts M, Slooter AJ, Van Gestel S, De Jonghe C, Vanderstichele H, Vanmechelen E, Breteler MM, Hofman A, van Duijn CM, Van Broeckhoven C. Dermaut B, et al. Am J Hum Genet. 1999 Jan;64(1):290-2. doi: 10.1086/302200. Am J Hum Genet. 1999. PMID: 9915968 Free PMC article. No abstract available.

3

Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretion.

De Jonghe C, Cruts M, Rogaeva EA, Tysoe C, Singleton A, Vanderstichele H, Meschino W, Dermaut B, Vanderhoeven I, Backhovens H, Vanmechelen E, Morris CM, Hardy J, Rubinsztein DC, St George-Hyslop PH, Van Broeckhoven C. De Jonghe C, et al. Among authors: dermaut b. Hum Mol Genet. 1999 Aug;8(8):1529-40. doi: 10.1093/hmg/8.8.1529. Hum Mol Genet. 1999. PMID: 10401002

4

Mutation screening of the tau gene in patients with early-onset Alzheimer's disease.

Roks G, Dermaut B, Heutink P, Julliams A, Backhovens H, Van de Broeck M, Serneels S, Hofman A, Van Broeckhoven C, van Duijn CM, Cruts M. Roks G, et al. Among authors: dermaut b. Neurosci Lett. 1999 Dec 24;277(2):137-9. doi: 10.1016/s0304-3940(99)00861-7. Neurosci Lett. 1999. PMID: 10624829

5

Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression.

Theuns J, Del-Favero J, Dermaut B, van Duijn CM, Backhovens H, Van den Broeck MV, Serneels S, Corsmit E, Van Broeckhoven CV, Cruts M. Theuns J, et al. Among authors: dermaut b. Hum Mol Genet. 2000 Feb 12;9(3):325-31. doi: 10.1093/hmg/9.3.325. Hum Mol Genet. 2000. PMID: 10655540 Free article.

6

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. J Neurol. 2000 May;247(5):364-8. doi: 10.1007/s004150050603. J Neurol. 2000. PMID: 10896268

7

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: dermaut b. Neurology. 2000 Sep 12;55(5):678-84. doi: 10.1212/wnl.55.5.678. Neurology. 2000. PMID: 10980733

8

Genetic testing should not be advocated as a diagnostic tool in familial forms of dementia.

Croes EA, Dermaut B, van Der Cammen TJ, van Broeckhoven C, van Duijn CM. Croes EA, et al. Among authors: dermaut b. Am J Hum Genet. 2000 Oct;67(4):1033-5. doi: 10.1086/303074. Am J Hum Genet. 2000. PMID: 10986048 Free PMC article. No abstract available.

9

Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions.

Van Goethem G, Dermaut B, Löfgren A, Martin JJ, Van Broeckhoven C. Van Goethem G, et al. Among authors: dermaut b. Nat Genet. 2001 Jul;28(3):211-2. doi: 10.1038/90034. Nat Genet. 2001. PMID: 11431686

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: 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.

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