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M Cruts

Showing results (71-80 of 80) with videos related to

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Neurology|April 14, 2004
The impact of APOE on myocardial infarction, stroke, and dementia: the Rotterdam StudyA J C Slooter, M Cruts, A Hofman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
Octapeptide repeat insertions in the prion protein gene and early onset dementiaE A Croes, J Theuns, J J Houwing-Duistermaat, et al.
Brain : a Journal of Neurology|September 27, 2000
Presentation of amyloidosis in carriers of the codon 692 mutation in the amyloid precursor protein gene (APP692)G Roks, F Van Harskamp, I De Koning, et al.
Brain : a Journal of Neurology|December 2, 2000
Pathology of early-onset Alzheimer's disease cases bearing the Thr113-114ins presenilin-1 mutationA B Singleton, R Hall, C G Ballard, et al.
Molecular Psychiatry|March 16, 2011
Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sitesN Brouwers, C Van Cauwenberghe, S Engelborghs, et al.
Human Molecular Genetics|July 13, 1999
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretionC De Jonghe, M Cruts, E A Rogaeva, et al.
Neurology|June 21, 2008
Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer diseaseN Brouwers, K Sleegers, S Engelborghs, et al.
Neurology|August 26, 2009
Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159HisJ van der Zee, D Pirici, T Van Langenhove, et al.
Neurology|January 11, 2008
Progranulin genetic variability contributes to amyotrophic lateral sclerosisK Sleegers, N Brouwers, S Maurer-Stroh, et al.
Molecular Psychiatry|October 21, 2015
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoterI Gijselinck, S Van Mossevelde, J van der Zee, et al.
Pageof 8

Showing results (71-80 of 80) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 80 results.
Neurology|April 14, 2004
The impact of APOE on myocardial infarction, stroke, and dementia: the Rotterdam StudyA J C Slooter, M Cruts, A Hofman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
Octapeptide repeat insertions in the prion protein gene and early onset dementiaE A Croes, J Theuns, J J Houwing-Duistermaat, et al.
Brain : a Journal of Neurology|September 27, 2000
Presentation of amyloidosis in carriers of the codon 692 mutation in the amyloid precursor protein gene (APP692)G Roks, F Van Harskamp, I De Koning, et al.
Brain : a Journal of Neurology|December 2, 2000
Pathology of early-onset Alzheimer's disease cases bearing the Thr113-114ins presenilin-1 mutationA B Singleton, R Hall, C G Ballard, et al.
Molecular Psychiatry|March 16, 2011
Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sitesN Brouwers, C Van Cauwenberghe, S Engelborghs, et al.
Human Molecular Genetics|July 13, 1999
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretionC De Jonghe, M Cruts, E A Rogaeva, et al.
Neurology|June 21, 2008
Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer diseaseN Brouwers, K Sleegers, S Engelborghs, et al.
Neurology|August 26, 2009
Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159HisJ van der Zee, D Pirici, T Van Langenhove, et al.
Neurology|January 11, 2008
Progranulin genetic variability contributes to amyotrophic lateral sclerosisK Sleegers, N Brouwers, S Maurer-Stroh, et al.
Molecular Psychiatry|October 21, 2015
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoterI Gijselinck, S Van Mossevelde, J van der Zee, et al.
Pageof 8