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Contribution of TARDBP to Alzheimer's Disease Genetic Etiology.
- Published in:
- Journal of Alzheimer's Disease, 2010, v. 21, n. 2, p. 423, doi. 10.3233/JAD-2010-100198
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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
Extended FTLD pedigree segregating a Belgian <italic>GRN</italic>-null mutation: neuropathological heterogeneity in one family.
- Published in:
- Alzheimer's Research & Therapy, 2018, v. 10, p. 1, doi. 10.1186/s13195-017-0334-y
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- Publication type:
- Article
Massive parallel gene panel sequencing in a belgian ftld cohort of causal genes associated with diverse neurodegenerative brain diseases.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P251, doi. 10.1016/j.jalz.2015.07.311
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- Publication type:
- Article
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
Geographical frequency of the FTLD-ALS causing C9orf72 repeat expansion mutation in an extended cohort ascertained within the European consortium on early-onset dementia
- Published in:
- 2012
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- Publication type:
- Abstract
Genomic characterization of the C9orf72 promoter repeat in FTLD and ALS patients
- Published in:
- 2012
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- Publication type:
- Abstract
The clinical presentation of C9orf72-associated frontotemporal lobar degeneration in an extended Flanders-Belgian cohort
- Published in:
- 2012
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- Publication type:
- Abstract
Risk For Alzheimer's Associated With A Copy Number Variation In The Complement Receptor 1 Increasing C3b/C4b Binding Sites
- Published in:
- 2011
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- Publication type:
- Abstract
Association of intermediate-length polyQ expansions in ATXN2 with ALS but not FTLD in a flanders-belgian cohort
- Published in:
- 2011
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- Publication type:
- Abstract
TMEM106B the first common risk factor for FTLD: Replication in a clinically diagnosed cohort of FTLD patients
- Published in:
- 2010
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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
P2-184: Identification of a novel chromosomal locus in a Belgian FTLD-MND family
- Published in:
- 2008
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- Publication type:
- Abstract
P3-395: Mean age-of-onset of familial Alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40
- Published in:
- 2006
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- Publication type:
- Abstract
P3-162: Increased variability of the tau gene MAPT due to genomic instability
- Published in:
- 2006
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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
P3-152: Direct evidence for a large inversion of the MAPT genomic region using fish of mechanically stretched chromosomes
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P3-149: An ancestral haplotype harbors a highly prevalent mutation for 17q21-linked tau-negative FTLD in Belgium
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P1-321: Contribution of dementia genes to Alzheimer’s disease in Belgium
- Published in:
- 2006
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- Publication type:
- Abstract
O2-02-08: Duplication of the APP locus in a Dutch family with early-onset Alzheimer dementia
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P3-395: Mean age-of-onset of familial Alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P3-162: Increased variability of the tau gene MAPT due to genomic instability
- 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
P3-152: Direct evidence for a large inversion of the MAPT genomic region using fish of mechanically stretched chromosomes
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P3-149: An ancestral haplotype harbors a highly prevalent mutation for 17q21-linked tau-negative FTLD in Belgium
- 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
O2-02-08: Duplication of the APP locus in a Dutch family with early-onset Alzheimer dementia
- Published in:
- 2006
- By:
- Publication type:
- Abstract
Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD.
- Published in:
- Scientific Reports, 2016, p. 20877, doi. 10.1038/srep20877
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- Publication type:
- Article
Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions: A Molecular Genetic Update.
- Published in:
- Neurodegenerative Diseases, 2007, v. 4, n. 2/3, p. 227, doi. 10.1159/000101847
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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
Diagnostic accuracy of the Preclinical AD Scale (PAS) in cognitively mildly impaired subjects.
- Published in:
- Journal of Neurology, 2002, v. 249, n. 3, p. 312, doi. 10.1007/s004150200011
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- Publication type:
- Article
Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertion.
- Published in:
- Journal of Neurology, 2000, v. 247, n. 5, p. 364, doi. 10.1007/s004150050603
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- Publication type:
- Article
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
Cholesterol and Triglycerides Moderate the Effect of Apolipoprotein E on Memory Functioning in Older Adults.
- Published in:
- Journals of Gerontology Series B: Psychological Sciences & Social Sciences, 2007, v. 62, n. 2, p. 112, doi. 10.1093/geronb/62.2.P112
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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
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
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
APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy.
- Published in:
- Brain: A Journal of Neurology, 2006, v. 129, n. 11, p. 2977, doi. 10.1093/brain/awl203
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- Publication type:
- Article
Reduced functional brain activity response in cognitively intact apolipoprotein E ɛ4 carriers.
- Published in:
- Brain: A Journal of Neurology, 2006, v. 129, n. 5, p. 1240, doi. 10.1093/brain/awl054
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- Publication type:
- Article
Reduced functional brain activity response in cognitively intact apolipoprotein E ɛ4 carriers.
- Published in:
- Brain: A Journal of Neurology, 2006, v. 129, n. 5, p. 1240, doi. 10.1093/brain/awl054
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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
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins.
- Published in:
- Nature Communications, 2014, v. 5, n. 9, p. 4835, doi. 10.1038/ncomms5835
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- Publication type:
- Article
Serum biomarker for progranulin-associated frontotemporal lobar degeneration.
- Published in:
- Annals of Neurology, 2009, v. 65, n. 5, p. 603, doi. 10.1002/ana.21621
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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
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
Correction to: Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins.
- Published in:
- 2024
- By:
- Publication type:
- Correction Notice
Bidirectional transcripts of the expanded <i>C9orf72</i> hexanucleotide repeat are translated into aggregating dipeptide repeat proteins.
- Published in:
- Acta Neuropathologica, 2013, v. 126, n. 6, p. 881, doi. 10.1007/s00401-013-1189-3
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- Publication type:
- Article
hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 3, p. 413, doi. 10.1007/s00401-013-1088-7
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- Publication type:
- Article