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The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease.
- Published in:
- Human Genetics, 2001, v. 108, n. 6, p. 552, doi. 10.1007/s004390100508
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- Publication type:
- Article
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.
- Published in:
- Nature, 2006, v. 442, n. 7105, p. 920, doi. 10.1038/nature05017
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- Publication type:
- Article
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 21, p. 3281, doi. 10.1093/hmg/ddi361
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- Publication type:
- Article
C-terminal TMEM106B fragments in human brain correlate with disease-associated TMEM106B haplotypes.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4055, doi. 10.1093/brain/awad133
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- Publication type:
- Article
Limbic-predominant age-related TDP-43 proteinopathy (LATE-NC) is associated with abundant TMEM106B pathology.
- Published in:
- Acta Neuropathologica, 2023, v. 146, n. 1, p. 163, doi. 10.1007/s00401-023-02580-2
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- Publication type:
- Article
Correction to: Accumulation of TMEM106B C‑terminal fragments in neurodegenerative disease and aging.
- Published in:
- 2023
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- Publication type:
- Correction Notice
Accumulation of TMEM106B C-terminal fragments in neurodegenerative disease and aging.
- Published in:
- Acta Neuropathologica, 2023, v. 145, n. 3, p. 285, doi. 10.1007/s00401-022-02531-3
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- Publication type:
- Article
Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 471, doi. 10.1038/sj.ejhg.5201986
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- Publication type:
- Article
Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sample.
- Published in:
- European Journal of Human Genetics, 1999, v. 7, n. 7, p. 801, doi. 10.1038/sj.ejhg.5200373
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- Publication type:
- Article
Novel PSEN1 Mutation in a Bulgarian Patient With Very Early-Onset Alzheimer's Disease, Spastic Paraparesis, and Extrapyramidal Signs.
- Published in:
- 2009
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- Publication type:
- Case Study
Loss-of-function mutations in TBK1 are frequently associated with frontotemporal lobar degeneration in a belgian patient cohort.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P333, doi. 10.1016/j.jalz.2015.08.157
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- Publication type:
- Article
Novel APP mutation p.E682K at the β’ processing site is associated with early-onset Alzheimer's disease
- Published in:
- 2009
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- Publication type:
- Abstract
P3-206: Genetic variability at the progranulin locus contributes to risk for Alzheimer's disease
- Published in:
- 2008
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- Publication type:
- Abstract
O2-05-02: VCP mutation in frontotemporal lobar degeneration with frequent TDP-43–positive intranuclear inclusions
- Published in:
- 2008
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- Publication type:
- Abstract
P3-159: MAPT H1 subhaplotyping in european PD association samples implicates tau splicing in early-onset parkinson’s disease susceptibility
- Published in:
- 2006
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- Publication type:
- Abstract
P1-321: Contribution of dementia genes to Alzheimer’s disease in Belgium
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P3-159: MAPT H1 subhaplotyping in european PD association samples implicates tau splicing in early-onset parkinson’s disease susceptibility
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P1-321: Contribution of dementia genes to Alzheimer’s disease in Belgium
- Published in:
- 2006
- By:
- Publication type:
- Abstract
Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.
- Published in:
- Human Mutation, 2009, v. 30, n. 7, p. 1054, doi. 10.1002/humu.21007
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- Publication type:
- Article
Progranulin null mutations in both sporadic and familial frontotemporal dementia.
- Published in:
- Human Mutation, 2007, v. 28, n. 9, p. 846, doi. 10.1002/humu.20520
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- Publication type:
- Article
Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort.
- Published in:
- 2016
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- Publication type:
- journal article
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort.
- Published in:
- Brain: A Journal of Neurology, 2011, v. 134, n. 3, p. 808, doi. 10.1093/brain/awr007
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- Publication type:
- Article
A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.
- Published in:
- Brain: A Journal of Neurology, 2006, v. 129, n. 4, p. 841, doi. 10.1093/brain/awl029
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- Publication type:
- Article
Novel APP mutation V715A associated with presenile Alzheimer’s disease in a German family.
- Published in:
- Journal of Neurology, 2003, v. 250, n. 11, p. 1374, doi. 10.1007/s00415-003-0182-5
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- Publication type:
- Article
α‐Synuclein promoter confers susceptibility to Parkinson's disease.
- Published in:
- Annals of Neurology, 2004, v. 56, n. 4, p. 591, doi. 10.1002/ana.20268
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- Publication type:
- Article
A novel presenilin 1 mutation associated with Pick's disease but not β-amyloid plaques.
- Published in:
- Annals of Neurology, 2004, v. 55, n. 5, p. 617
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- Publication type:
- Article
Early cognitive decline is associated with prion protein codon 129 polymorphism.
- Published in:
- Annals of Neurology, 2003, v. 54, n. 2, p. 275
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- Publication type:
- Article
PRNP Val129 homozygosity increases risk for early-onset Alzheimer's disease.
- Published in:
- Annals of Neurology, 2003, v. 53, n. 3, p. 409
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- Publication type:
- Article
Why female crested tits copulate repeatedly with the same partner: evidence for the mate assessment hypothesis
- Published in:
- Behavioral Ecology, 1997, v. 8, n. 1, p. 87, doi. 10.1093/beheco/8.1.87
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- Publication type:
- Article
Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion.
- Published in:
- JAMA Neurology, 2017, v. 74, n. 4, p. 445, doi. 10.1001/jamaneurol.2016.4847
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- Publication type:
- Article
Distinct Clinical Characteristics of C9orf72 Expansion Carriers Compared With GRN, MAPT, and Nonmutation Carriers in a Flanders-Belgian FTLD Cohort.
- Published in:
- JAMA Neurology, 2013, v. 70, n. 3, p. 365, doi. 10.1001/2013.jamaneurol.181
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- Publication type:
- Article
Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 1, p. 43, doi. 10.1093/hmg/7.1.43
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- Publication type:
- Article