Lista de obras -

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

artículo científico publicado en 2011

A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease

artículo científico publicado en 2016

A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies

artículo científico publicado en 2013

A systematic review comparing the diagnostic value of 14-3-3 protein in the cerebrospinal fluid, RT-QuIC and RT-QuIC on nasal brushing in sporadic Creutzfeldt-Jakob disease

artículo científico publicado en 2018

Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family.

artículo científico publicado en 2007

Alzheimer's disease and driving: review of the literature and consensus guideline from Belgian dementia experts and the Belgian road safety institute endorsed by the Belgian Medical Association

artículo científico publicado en 2017

Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts

artículo científico publicado en 2011

Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion

artículo científico publicado en 2017

Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

artículo científico publicado en 2015

Clinical variability and onset age modifiers in an extended Belgian GRN founder family.

artículo científico publicado en 2018

Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population

artículo científico publicado en 2012

DLB and PDD: a role for mutations in dementia and Parkinson disease genes?

artículo científico publicado en 2011

Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease

artículo científico publicado en 2017

Diagnostic performance of a CSF-biomarker panel in autopsy-confirmed dementia.

artículo científico publicado en 2007

Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degeneration.

artículo científico publicado en 2018

Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort

artículo científico publicado en 2013

Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients

artículo científico publicado en 2013

GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population

artículo científico publicado en 2009

Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease

artículo científico publicado en 2008

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease

artículo científico publicado en 2014

Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystonia

artículo científico publicado en 2012

Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis

artículo científico publicado en 2010

Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients

artículo científico publicado en 2016

Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains

artículo científico publicado en 2015

Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia

artículo científico publicado en 2013

Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability.

artículo científico publicado en 2019

Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort

artículo científico publicado en 2015

Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD.

scientific article published on 16 September 2016

Neuronal RNA oxidation is a prominent feature of familial Alzheimer's disease

artículo científico publicado en 2004

No added diagnostic value of non-phosphorylated tau fraction (p-taurel) in CSF as a biomarker for differential dementia diagnosis

artículo científico publicado en 2017

No association of CSF biomarkers with APOEepsilon4, plaque and tangle burden in definite Alzheimer's disease

artículo científico publicado en 2007

No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

article

Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

artículo científico publicado en 2016

Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort

artículo científico publicado en 2015

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

artículo científico publicado en 2014

Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia.

artículo científico publicado en 2018

Redox metals and oxidative abnormalities in human prion diseases

artículo científico publicado en 2005

Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population

artículo científico publicado en 2009

TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

scientific article published on 23 December 2016

TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions

artículo científico publicado en 2014

TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort

artículo científico publicado en 2011

The genetics and neuropathology of frontotemporal lobar degeneration

artículo científico publicado en 2012

Lista de obras de

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease

A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies

A systematic review comparing the diagnostic value of 14-3-3 protein in the cerebrospinal fluid, RT-QuIC and RT-QuIC on nasal brushing in sporadic Creutzfeldt-Jakob disease

Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family.

Alzheimer's disease and driving: review of the literature and consensus guideline from Belgian dementia experts and the Belgian road safety institute endorsed by the Belgian Medical Association

Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts

Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion

Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

Clinical variability and onset age modifiers in an extended Belgian GRN founder family.

Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population

DLB and PDD: a role for mutations in dementia and Parkinson disease genes?

Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease

Diagnostic performance of a CSF-biomarker panel in autopsy-confirmed dementia.

Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degeneration.

Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort

Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients

GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population

Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease

Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystonia

Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis

Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients

Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains

Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia

Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability.

Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort

Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD.

Neuronal RNA oxidation is a prominent feature of familial Alzheimer's disease

No added diagnostic value of non-phosphorylated tau fraction (p-taurel) in CSF as a biomarker for differential dementia diagnosis

No association of CSF biomarkers with APOEepsilon4, plaque and tangle burden in definite Alzheimer's disease

No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia.

Redox metals and oxidative abnormalities in human prion diseases

Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population

TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions

TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort

The genetics and neuropathology of frontotemporal lobar degeneration