(Q41748096)

8 October 2017

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title

Role of genetics in tests of genotype, status, and disease progression in early-onset Alzheimer's disease (English)

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8 October 2017

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St George-Hyslop PH

1

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8 October 2017

publication date

1 March 1998

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8 October 2017

published in

Neurobiology of Aging

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8 October 2017

volume

19

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8 October 2017

issue

2

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8 October 2017

page(s)

133-137

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Apolipoprotein E genotyping in the diagnosis of alzheimer's disease: A cautionary view

8 October 2017

cites work

1 reference

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Mutations of the presenilin I gene in families with early-onset Alzheimer's disease

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7 January 2021

More missense in amyloid gene.

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7 January 2021

Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene

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7 January 2021

Screening for the beta-amyloid precursor protein mutation (APP717: Val----Ile) in extended pedigrees with early onset Alzheimer's disease.

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7 January 2021

The presenilin genes: a new gene family involved in Alzheimer disease pathology

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7 January 2021

Molecular genetic analysis of familial early-onset Alzheimer's disease linked to chromosome 14q24.3.

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7 January 2021

Alzheimer's disease: clinical implications of the apolipoprotein E genotype

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7 January 2021

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

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7 January 2021

The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part X. Neuropathology confirmation of the clinical diagnosis of Alzheimer's disease

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7 January 2021

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

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7 January 2021

Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein gene.

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7 January 2021

The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients.

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Mutation in codon 713 of the β amyloid precursor protein gene presenting with schizophrenia

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7 January 2021

Three different mutations of presenilin 1 gene in early-onset Alzheimer's disease families

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7 January 2021

Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein gene

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7 January 2021

Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype.

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7 January 2021

Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type.

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7 January 2021

A familial Alzheimer's disease locus on chromosome 1.

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

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7 January 2021

A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease

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7 January 2021

Mis-sense mutation Val&rarr;Ile in exon 17 of amyloid precursor protein gene in Japanese familial Alzheimer's disease

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7 January 2021

Novel polymorphism in the A4 region of the amyloid precursor protein gene in a patient without Alzheimer's disease.

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7 January 2021

Novel amyloid precursor protein gene mutation (codon 665Asp) in a patient with late-onset Alzheimer's disease

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7 January 2021

Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

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7 January 2021

Apolipoprotein E genotyping in the differential diagnosis, not prediction, of Alzheimer's disease

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7 January 2021

Chemical cleavage of mismatch to detect mutations

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7 January 2021

Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease

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7 January 2021

Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant.

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7 January 2021

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

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7 January 2021

The use of chemical reagents in the detection of DNA mutations.

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7 January 2021

Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's disease

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7 January 2021

Alzheimer's disease and possible gene interaction.

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7 January 2021

Sequence analysis of presenilin-1 gene mutation in Japanese Alzheimer's disease patients.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Failure to detect missense mutations in the S182 gene in a series of late-onset Alzheimer's disease cases.

1 reference

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7 January 2021

Presenilins and Alzheimer disease

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7 January 2021

Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease. Alzheimer's Disease Collaborative Group

1 reference

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7 January 2021

Risk of dementia among relatives of Alzheimer's disease patients in the MIRAGE study: What is in store for the oldest old?

1 reference

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7 January 2021

10.1016/S0197-4580(98)00020-7

Identifiers

DOI

1 reference

8 October 2017

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