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Strain-balanced InGaN/GaN multiple quantum wells

Applied physics letters, 2014-07, Vol.105 (3)

2014

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The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter

Molecular psychiatry, 2016-08, Vol.21 (8), p.1112-1124

2016

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Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease

Human molecular genetics, 1998-01, Vol.7 (1), p.43-51

1998

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Genetic contribution of FUS to frontotemporal lobar degeneration

Neurology, 2010-02, Vol.74 (5), p.366

2010

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Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval

Molecular psychiatry, 2002-01, Vol.7 (10), p.1064-1074

2002

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Progranulin genetic variability contributes to amyotrophic lateral sclerosis

Neurology, 2008-07, Vol.71 (4), p.253

2008

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Assessment of activated sludge stability in lab-scale experiments

Journal of biotechnology, 2009-05, Vol.141 (3), p.147-154

2009

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Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease

Neurology, 2008-08, Vol.71 (9), p.656

2008

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Inversion by metalorganic chemical vapor deposition from N- to Ga-polar gallium nitride and its application to multiple quantum well light-emitting diodes

Applied physics letters, 2013-12, Vol.103 (23)

2013

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Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His

Neurology, 2009-08, Vol.73 (8), p.626

2009

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High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy

Human molecular genetics, 2005-11, Vol.14 (21), p.3281-3292

2005

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Alzheimer dementia caused by a novel mutation located in the APP C‐terminal intracytosolic fragment

Human mutation, 2006-09, Vol.27 (9), p.888-896

2006

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Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects

Journal of neurology, neurosurgery and psychiatry, 2003-08, Vol.74 (8), p.1148-1151

2003

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Octapeptide repeat insertions in the prion protein gene and early onset dementia

Journal of neurology, neurosurgery and psychiatry, 2004-08, Vol.75 (8), p.1166-1170

2004

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Alzheimer dementia caused by a novel mutation located in the APP C-terminal intracytosolic fragment

Human mutation, 2006-09, Vol.27 (9), p.888-896

2006

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Legal framework and current techniques for age estimation in puppy trade

Vlaams diergeneeskundig tijdschrift, 2020-06, Vol.89 (3), p.135-144

2020

Volltextzugriff (PDF)

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

Human molecular genetics, 2000-02, Vol.9 (3), p.325-331

2000

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Fabry disease in a patient with Turner syndrome

Journal of inherited metabolic disease, 2009-12, Vol.32 (Suppl 1), p.45-48

2009

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Association of cyclin-dependent kinase 5 and neuronal activators p35 and p39 complex in early-onset Alzheimer's disease

Neurobiology of aging, 2005-08, Vol.26 (8), p.1145-1151

2005

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α-Synuclein promoter confers susceptibility to Parkinson's disease

Annals of neurology, 2004-10, Vol.56 (4), p.591-595

2004

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Pure progressive amnesia as variant of genetically proven Alzheimer disease

European journal of neurology, 2009-02, Vol.16 (2), p.e9-e10

2009

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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Acta neuropathologica, 2014-09, Vol.128 (3), p.397-410

2014

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Compaction control and related stress–strain behaviour of off-shore land reclamations with calcareous sands

Soils and foundations, 2015-12, Vol.55 (6), p.1474-1486

2015

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Dissociation between verbal response initiation and suppression after prefrontal lesions

Cerebral cortex (New York, N.Y. 1991), 2012-10, Vol.22 (10), p.2428-2440

2012

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Strain-balanced InGaN/GaN multiple quantum wells

The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter

Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease

Genetic contribution of FUS to frontotemporal lobar degeneration

Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval

Progranulin genetic variability contributes to amyotrophic lateral sclerosis

Assessment of activated sludge stability in lab-scale experiments

Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease

Inversion by metalorganic chemical vapor deposition from N- to Ga-polar gallium nitride and its application to multiple quantum well light-emitting diodes

Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His

High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy

Alzheimer dementia caused by a novel mutation located in the APP C‐terminal intracytosolic fragment

Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects

Octapeptide repeat insertions in the prion protein gene and early onset dementia

Alzheimer dementia caused by a novel mutation located in the APP C-terminal intracytosolic fragment

Legal framework and current techniques for age estimation in puppy trade

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

Fabry disease in a patient with Turner syndrome

Association of cyclin-dependent kinase 5 and neuronal activators p35 and p39 complex in early-onset Alzheimer's disease

α-Synuclein promoter confers susceptibility to Parkinson's disease

Pure progressive amnesia as variant of genetically proven Alzheimer disease

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Management of prostate cancer in older patients: updated recommendations of a working group of the International Society of Geriatric Oncology

Compaction control and related stress–strain behaviour of off-shore land reclamations with calcareous sands

Dissociation between verbal response initiation and suppression after prefrontal lesions

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