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The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Aβ protofibril formation

Nature neuroscience, 2001-09, Vol.4 (9), p.887-893

2001

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A Unique Gene Expression Signature Discriminates Familial Alzheimer's Disease Mutation Carriers from Their Wild-Type Siblings

Proceedings of the National Academy of Sciences - PNAS, 2005-10, Vol.102 (41), p.14854-14859

2005

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A mutation in Alzheimerʼs disease destroying a splice acceptor site in the presenilin-1 gene

Neuroreport, 1995-12, Vol.7 (1), p.297-301

1995

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Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family

Alzheimer's & dementia, 2008-11, Vol.4 (6), p.414-420

2008

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Interaction between estrogen receptor 1 and the ε4 allele of apolipoprotein E increases the risk of familial Alzheimer's disease in women

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

2000

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No association between polymorphisms in the neprilysin promoter region and Swedish Alzheimer's disease patients

Neuroscience letters, 2003-02, Vol.337 (2), p.111-113

2003

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Interaction between estrogen receptor 1 and the epsilon 4 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

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Tau gene polymorphisms and apolipoprotein E ε4 may interact to increase risk for Alzheimer’s disease

Neuroscience letters, 1999-12, Vol.277 (1), p.29-32

1999

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Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21

American journal of medical genetics, 1997-07, Vol.74 (4), p.380-385

1997

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Apolipoprotein ε4 allele in swedish twins and siblings with Alzheimer disease

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

1995

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Tau gene polymorphisms and apolipoprotein E epsilon 4 may interact to increase risk for Alzheimer's disease

Neuroscience letters, 1999-12, Vol.277 (1), p.29-32

1999

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Clinical findings in nondemented mutation carriers predisposed to Alzheimer's disease: a model of mild cognitive impairment

Acta neurologica Scandinavica, 2003, Vol.107 (s179), p.77-82

2003

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49 Variable age of onset in an alzheimer family with a His163Tyr mutation in the presenilin 1 gene

Neurobiology of aging, 1996, Vol.17 (4), p.S13-S13

1996

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Apolipoprotein E and α1-Antichymotrypsin Genotypes and Age of Onset of Familial Alzheimer’s Disease

Dementia and geriatric cognitive disorders, 1999, Vol.10 (1), p.1-5

1999

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A novel pathogenic mutation (Leu262Phe) found in the presenilin 1 gene in early-onset Alzheimer's disease

Neuroscience letters, 1997-09, Vol.234 (1), p.3-6

1997

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Genome scan on Swedish Alzheimer's disease multiplex families

NEUROBIOLOGY OF AGING, 2004, Vol.25, p.S493

2004

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FDG PET reveals decreased cerebral glucose metabolism in presymptomatic carriers of the His163Tyr mutation in the presentlin-1 gene at risk for developing familial Alzheimer's disease

NEUROBIOLOGY OF AGING, 2004, Vol.25, p.S377

2004

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The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Abeta protofibril formation

Nature neuroscience, 2001-09, Vol.4 (9), p.887-893

2001

Volltextzugriff (PDF)

No linkage to chromosome 14 in Swedish Alzheimer's disease families

Nature genetics, 1993-07, Vol.4 (3), p.218-219

1993

Volltextzugriff (PDF)

Tau gene polymorphisms and apolipoprotein E epsilon4 may interact to increase risk for Alzheimer's disease

Neuroscience letters, 1999-12, Vol.277 (1), p.29-32

1999

Volltextzugriff (PDF)

Neuroimaging and cognitive features of familial Alzheimer's disease

NEUROBIOLOGY OF AGING, 2002, Vol.23 (1), p.S357

2002

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Low frequency of the APP 670/671 mutation in familial Alzheimer's disease in Sweden

Neuroscience letters, 1993-04, Vol.153 (1), p.85-87

1993

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Abnormalities in cerebral glucose metabolism of familial Alzheimer's disease associated with 670/671 APP mutation and presenilin 1 gene mutations

NEUROBIOLOGY OF AGING, 2002, Vol.23 (1), p.S479

2002

Volltextzugriff (PDF)

Conversion from preclinical to dinical stage of Alzheimer's disease as shown by decline of cognitive function in carriers of the Swedish APP-mutation

Journal of neural transmission. Supplementum, 2002 (62), p.117

2002

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The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Aβ protofibril formation

A Unique Gene Expression Signature Discriminates Familial Alzheimer's Disease Mutation Carriers from Their Wild-Type Siblings

The structure of the presenilin 1 ( S182 ) gene and identification of six novel mutations in early onset AD families

A mutation in Alzheimerʼs disease destroying a splice acceptor site in the presenilin-1 gene

Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family

Interaction between estrogen receptor 1 and the ε4 allele of apolipoprotein E increases the risk of familial Alzheimer's disease in women

No association between polymorphisms in the neprilysin promoter region and Swedish Alzheimer's disease patients

Interaction between estrogen receptor 1 and the epsilon 4 allele of apolipoprotein E increases the risk of familial Alzheimer's disease in women

Tau gene polymorphisms and apolipoprotein E ε4 may interact to increase risk for Alzheimer’s disease

Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21

Apolipoprotein ε4 allele in swedish twins and siblings with Alzheimer disease

Tau gene polymorphisms and apolipoprotein E epsilon 4 may interact to increase risk for Alzheimer's disease

Clinical findings in nondemented mutation carriers predisposed to Alzheimer's disease: a model of mild cognitive impairment

49 Variable age of onset in an alzheimer family with a His163Tyr mutation in the presenilin 1 gene

Apolipoprotein E and α1-Antichymotrypsin Genotypes and Age of Onset of Familial Alzheimer’s Disease

A novel pathogenic mutation (Leu262Phe) found in the presenilin 1 gene in early-onset Alzheimer's disease

Genome scan on Swedish Alzheimer's disease multiplex families

FDG PET reveals decreased cerebral glucose metabolism in presymptomatic carriers of the His163Tyr mutation in the presentlin-1 gene at risk for developing familial Alzheimer's disease

The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Abeta protofibril formation

No linkage to chromosome 14 in Swedish Alzheimer's disease families

Tau gene polymorphisms and apolipoprotein E epsilon4 may interact to increase risk for Alzheimer's disease

Neuroimaging and cognitive features of familial Alzheimer's disease

Low frequency of the APP 670/671 mutation in familial Alzheimer's disease in Sweden

Abnormalities in cerebral glucose metabolism of familial Alzheimer's disease associated with 670/671 APP mutation and presenilin 1 gene mutations

Conversion from preclinical to dinical stage of Alzheimer's disease as shown by decline of cognitive function in carriers of the Swedish APP-mutation

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