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Genome scan on Swedish Alzheimer's disease families

Molecular psychiatry, 2006-02, Vol.11 (2), p.182-186

2006

Volltextzugriff (PDF)

Predicting Cognitive Decline across Four Decades in Mutation Carriers and Non-carriers in Autosomal-Dominant Alzheimer’s Disease

Journal of the International Neuropsychological Society, 2017-03, Vol.23 (3), p.195-203

2017

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Clinical and neuropathological features of the arctic APP gene mutation causing early-onset Alzheimer disease

Archives of neurology (Chicago), 2008-04, Vol.65 (4), p.499

2008

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Glucose metabolism and PIB binding in carriers of a His163Tyr presenilin 1 mutation

Neurobiology of aging, 2011-08, Vol.32 (8), p.1388-1399

2011

Volltextzugriff (PDF)

Genetic association to the amyloid plaque associated protein gene COL25A1 in Alzheimer's disease

Neurobiology of aging, 2010-03, Vol.31 (3), p.409-415

2010

Volltextzugriff (PDF)

A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of β-amyloid

Nature genetics, 1992-08, Vol.1 (5), p.345-347

1992

Volltextzugriff (PDF)

Genetic counseling in a Swedish Alzheimer family with amyloid precursor protein mutation

American journal of human genetics, 1995-01, Vol.56 (1), p.332-335

1995

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Expanded high-resolution genetic study of 109 Swedish families with Alzheimer's disease

European journal of human genetics : EJHG, 2008-02, Vol.16 (2), p.202-208

2008

Volltextzugriff (PDF)

Wide range of disease onset in a family with Alzheimer disease and a His163Tyr mutation in the presenilin-1 gene

Archives of neurology (Chicago), 1998-05, Vol.55 (5), p.698

1998

Volltextzugriff (PDF)

No evidence of linkage to chromosome 9q21–22 in a Swedish family with frontotemporal dementia and amyotrophic lateral sclerosis

Neuroscience letters, 2003-04, Vol.340 (3), p.245-247

2003

Volltextzugriff (PDF)

Life situation, coping and quality of life in people with high and low risk of developing Alzheimer's disease

Dementia and geriatric cognitive disorders, 2003-01, Vol.16 (4), p.220-228

2003

Volltextzugriff (PDF)

Investigations of a CA repeat in the oestrogen receptor beta gene in patients with Alzheimer's disease

European journal of human genetics : EJHG, 2001-10, Vol.9 (10), p.802-804

2001

Volltextzugriff (PDF)

Clinical characteristics of a chromosome 17-linked rapidly progressive familial frontotemporal dementia

Archives of neurology (Chicago), 1997-05, Vol.54 (5), p.539-544

1997

Volltextzugriff (PDF)

Amyloid precursor protein mutation causes Alzheimer's disease in a Swedish family

Neuroscience letters, 1994-02, Vol.168 (1), p.254-256

1994

Volltextzugriff (PDF)

Chromosome 14-encoded Alzheimer's disease: Genetic and clinicopathological description

Annals of neurology, 1994-09, Vol.36 (3), p.362-367

1994

Volltextzugriff (PDF)

A follow-up study of the family with the Swedish APP 670/671 Alzheimer's disease mutation

Dementia and geriatric cognitive disorders, 1999-11, Vol.10 (6), p.526-533

1999

Volltextzugriff (PDF)

Apolipoprotein E and alpha1-antichymotrypsin genotypes and age of onset of familial Alzheimer's disease

Dementia and geriatric cognitive disorders, 1999-01, Vol.10 (1), p.1

1999

Volltextzugriff (PDF)

Interaction between estrogen receptor 1 and the epsilon4 allele of apolipoprotein E increases the risk of familial Alzheimer's disease in women

Neuroscience letters, 2000-03, Vol.282 (1-2), p.45-48

2000

Volltextzugriff (PDF)

Apolipoprotein epsilon 4 allele in Swedish twins and siblings with Alzheimer disease

Alzheimer disease and associated disorders, 1995, Vol.9 (3), p.166-169

1995

Volltextzugriff (PDF)

Allelic association but only weak evidence for linkage to the apolipoprotein E locus in late-onset Swedish Alzheimer families

American journal of medical genetics, 1996-05, Vol.67 (3), p.306-311

1996

Volltextzugriff (PDF)

Dynamics of lipids and polychlorinated biphenyls in a baltic amphipod (Monoporeia affinis): A field study

Environmental toxicology and chemistry, 2003-10, Vol.22 (10), p.2499-2507

2003

Volltextzugriff (PDF)

Selection against lethal alleles in females heterozygous for incontinentia pigmenti

American journal of human genetics, 1989, Vol.44 (1), p.100-106

1989

Volltextzugriff (PDF)

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Genome scan on Swedish Alzheimer's disease families

Predicting Cognitive Decline across Four Decades in Mutation Carriers and Non-carriers in Autosomal-Dominant Alzheimer’s Disease

Clinical and neuropathological features of the arctic APP gene mutation causing early-onset Alzheimer disease

Glucose metabolism and PIB binding in carriers of a His163Tyr presenilin 1 mutation

Genetic association to the amyloid plaque associated protein gene COL25A1 in Alzheimer's disease

A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of β-amyloid

Genetic counseling in a Swedish Alzheimer family with amyloid precursor protein mutation

Expanded high-resolution genetic study of 109 Swedish families with Alzheimer's disease

Wide range of disease onset in a family with Alzheimer disease and a His163Tyr mutation in the presenilin-1 gene

No evidence of linkage to chromosome 9q21–22 in a Swedish family with frontotemporal dementia and amyotrophic lateral sclerosis

Life situation, coping and quality of life in people with high and low risk of developing Alzheimer's disease

Investigations of a CA repeat in the oestrogen receptor beta gene in patients with Alzheimer's disease

Clinical characteristics of a chromosome 17-linked rapidly progressive familial frontotemporal dementia

Amyloid precursor protein mutation causes Alzheimer's disease in a Swedish family

Chromosome 14-encoded Alzheimer's disease: Genetic and clinicopathological description

A follow-up study of the family with the Swedish APP 670/671 Alzheimer's disease mutation

Apolipoprotein E and alpha1-antichymotrypsin genotypes and age of onset of familial Alzheimer's disease

Interaction between estrogen receptor 1 and the epsilon4 allele of apolipoprotein E increases the risk of familial Alzheimer's disease in women

Apolipoprotein epsilon 4 allele in Swedish twins and siblings with Alzheimer disease

Allelic association but only weak evidence for linkage to the apolipoprotein E locus in late-onset Swedish Alzheimer families

Dynamics of lipids and polychlorinated biphenyls in a baltic amphipod (Monoporeia affinis): A field study

Selection against lethal alleles in females heterozygous for incontinentia pigmenti

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