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

Archives of neurology (Chicago), 2007-10, Vol.64 (10), p.1436

2007

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Non-motor symptoms in a Flanders-Belgian population of 215 Parkinson's disease patients as assessed by the Non-Motor Symptoms Questionnaire

American journal of neurodegenerative disease, 2012, Vol.1 (2), p.160-167

2012

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The genetics of dementia with Lewy bodies: what are we missing?

Archives of neurology (Chicago), 2012-09, Vol.69 (9), p.1113

2012

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SNPbox: web-based high-throughput primer design with an eye for repetitive sequences

Methods in molecular biology (Clifton, N.J.), 2007, Vol.402, p.179

2007

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

Archives of neurology (Chicago), 2010-05, Vol.67 (5), p.606

2010

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Tracing myelin protein zero (P0) in vivo by construction of P0-GFP fusion proteins

BMC cell biology, 2002-11, Vol.3 (1), p.29, Article 29

2002

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Risk estimates of dementia by apolipoprotein E genotypes from a population-based incidence study: the Rotterdam Study

Archives of neurology (Chicago), 1998-07, Vol.55 (7), p.964

1998

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Association study of bipolar disorder with candidate genes involved in catecholamine neurotransmission: DRD2, DRD3, DAT1, and TH genes

American journal of medical genetics, 1996-11, Vol.67 (6), p.551-555

1996

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Association of brain-specific tryptophan hydroxylase, TPH2, with unipolar and bipolar disorder in a Northern Swedish, isolated population

Archives of general psychiatry, 2006-10, Vol.63 (10), p.1103

2006

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A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotype

Archives of neurology (Chicago), 1999-10, Vol.56 (10), p.1283

1999

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Systematic genetic study of Alzheimer disease in Latin America: Mutation frequencies of the amyloid ? precursor protein and presenilin genes in Colombia

American journal of medical genetics, 2001-10, Vol.103 (2), p.138-143

2001

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Molecular pathogenesis of frontotemporal lobar degeneration: basic science seminar in neurology

Archives of neurology (Chicago), 2008-06, Vol.65 (6), p.700

2008

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A Major Genetic Factor at Chromosome 9p Implicated in Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Lobar Degeneration (FTLD)

Gijselinck, Ilse

2012

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Chapter 23 Alzheimer's disease: Identification of genes and genetic risk factors

Progress in Brain Research, 1998, Vol.117, p.315-325

Broeckhoven, Christine Van

1998

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Neurogenetics of Dementia

Biological Psychiatry, 2002, p.361-375

2002

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Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frameshift mutation

Parkinsonism & related disorders, 2011, Vol.17 (2), p.135-138

2011

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PROPERTIES OF 5-MERCURIPYRIMIDINE RIBONUCLEOTIDES AND OF MERCURATED RIBONUCLEIC ACIDS (DUTCH TEXT)

VAN BROECKHOVEN, CHRISTINE LEONA

1980

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Systematic genetic study of Alzheimer disease in Latin America: Mutation frequencies of the amyloid β precursor protein and presenilin genes in Colombia

American journal of medical genetics, 2001-10, Vol.103 (2), p.138-143

2001

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β‐Amyloid Precursor Protein and Early‐Onset Alzheimer's Disease

Ciba Foundation Symposium 199 ‐ The Nature and Origin of Amyloid Fibrils, 2007, p.170-180

2007

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CHAPTER 5.6 Identification and functional analysis of genes and genetic risk factors in Alzheimer's disease

Techniques in the Behavioral and Neural Sciences, 1999, Vol.13, p.841-862

1999

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Abstracts for the Xth World Congress of Psychiatric Genetics, Brussels, Belgium, October 9-13, 2002

American journal of medical genetics, 2002, Vol.114 (7)

2002

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Efficient generation of stably electrotransfected human hematopoietic cell lines without drug selection by consecutive FACsorting

Cytometry (New York, N.Y.), 2000-09, Vol.41 (1), p.31-35

2000

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Novel APP mutation V715A associated with presenile Alzheimer's disease in a German family

Journal of neurology, 2003, Vol.250 (11), p.1374-1375

2003

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An adhesion test system based on Schneider cells to determine genotype–phenotype correlations for mutated P0 proteins

Genetic analysis : biomolecular engineering, 1998-10, Vol.14 (4), p.117-119

1998

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

Non-motor symptoms in a Flanders-Belgian population of 215 Parkinson's disease patients as assessed by the Non-Motor Symptoms Questionnaire

The genetics of dementia with Lewy bodies: what are we missing?

Meta-analysis of the association between variants in SORL1 and Alzheimer disease

SNPbox: web-based high-throughput primer design with an eye for repetitive sequences

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

Tracing myelin protein zero (P0) in vivo by construction of P0-GFP fusion proteins

Risk estimates of dementia by apolipoprotein E genotypes from a population-based incidence study: the Rotterdam Study

Association study of bipolar disorder with candidate genes involved in catecholamine neurotransmission: DRD2, DRD3, DAT1, and TH genes

Association of brain-specific tryptophan hydroxylase, TPH2, with unipolar and bipolar disorder in a Northern Swedish, isolated population

A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotype

Systematic genetic study of Alzheimer disease in Latin America: Mutation frequencies of the amyloid ? precursor protein and presenilin genes in Colombia

Molecular pathogenesis of frontotemporal lobar degeneration: basic science seminar in neurology

A Major Genetic Factor at Chromosome 9p Implicated in Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Lobar Degeneration (FTLD)

Chapter 23 Alzheimer's disease: Identification of genes and genetic risk factors

Neurogenetics of Dementia

Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frameshift mutation

PROPERTIES OF 5-MERCURIPYRIMIDINE RIBONUCLEOTIDES AND OF MERCURATED RIBONUCLEIC ACIDS (DUTCH TEXT)

Systematic genetic study of Alzheimer disease in Latin America: Mutation frequencies of the amyloid β precursor protein and presenilin genes in Colombia

β‐Amyloid Precursor Protein and Early‐Onset Alzheimer's Disease

CHAPTER 5.6 Identification and functional analysis of genes and genetic risk factors in Alzheimer's disease

Abstracts for the Xth World Congress of Psychiatric Genetics, Brussels, Belgium, October 9-13, 2002

Efficient generation of stably electrotransfected human hematopoietic cell lines without drug selection by consecutive FACsorting

Novel APP mutation V715A associated with presenile Alzheimer's disease in a German family

An adhesion test system based on Schneider cells to determine genotype–phenotype correlations for mutated P0 proteins

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