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Early-onset familial Alzheimer's disease (EOFAD).
scientific article published on July 2012
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Europe PubMed Central
PubMed publication ID
22728850
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
title
Early-onset familial Alzheimer's disease (EOFAD)
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22728850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
main subject
Alzheimer's disease
0 references
author
Jianping Jia
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22728850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728850%20AND%20SRC:MED&resulttype=core&format=json
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6 February 2020
Sandra Black
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6
object named as
Sandra E Black
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22728850
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6 February 2020
author name string
Liyong Wu
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1
1 reference
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Europe PubMed Central
PubMed publication ID
22728850
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728850%20AND%20SRC:MED&resulttype=core&format=json
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6 February 2020
Ging-Yuek R Hsiung
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3
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Europe PubMed Central
PubMed publication ID
22728850
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retrieved
6 February 2020
A Dessa Sadovnick
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22728850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
Mario Masellis
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22728850
reference URL
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retrieved
6 February 2020
Serge Gauthier
series ordinal
8
1 reference
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Europe PubMed Central
PubMed publication ID
22728850
reference URL
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retrieved
6 February 2020
Pedro Rosa-Neto
series ordinal
2
1 reference
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Europe PubMed Central
PubMed publication ID
22728850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
publication date
1 July 2012
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22728850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
published in
Canadian Journal of Neurological Sciences
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22728850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
volume
39
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22728850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22728850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
page(s)
436-445
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22728850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
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Alzheimer's disease with spastic paraparesis and 'cotton wool' plaques: two pedigrees with PS-1 exon 9 deletions
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7 January 2021
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Frequency of mutations in the presenilin and amyloid precursor protein genes in early-onset Alzheimer disease in Spain.
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7 January 2021
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Tracking atrophy progression in familial Alzheimer's disease: a serial MRI study
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Clinical features of early-onset Alzheimer disease in a large kindred with an E280A presenilin-1 mutation
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High striatal amyloid beta-peptide deposition across different autosomal Alzheimer disease mutation types
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Histopathological and molecular heterogeneity among individuals with dementia associated with Presenilin mutations
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Change in rates of cerebral atrophy over time in early-onset Alzheimer's disease: longitudinal MRI study
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An increased percentage of long amyloid beta protein secreted by familial amyloid beta protein precursor (beta APP717) mutants.
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Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
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Hippocampal hyperactivation in presymptomatic familial Alzheimer's disease
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Disease-modifying therapies for Alzheimer disease: challenges to early intervention
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Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein gene.
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Variant Alzheimer disease with spastic paraparesis: neuropathological phenotype
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Impact of DNA testing for early-onset familial Alzheimer disease and frontotemporal dementia
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Identification of independent APP locus duplication in Japanese patients with early-onset Alzheimer disease
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Mutational analysis in early-onset familial dementia in the Japanese population. The role of PSEN1 and MAPT R406W mutations.
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based on heuristic
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A novel PSEN2 mutation associated with a peculiar phenotype
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7 January 2021
based on heuristic
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Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Phosphorylation of paired helical filament tau in Alzheimer's disease neurofibrillary lesions: focusing on phosphatases
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7 January 2021
based on heuristic
inferred from DOI database lookup
The genetic defect causing familial Alzheimer's disease maps on chromosome 21.
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
1 reference
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https://api.crossref.org/works/10.1017%2FS0317167100013949
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based on heuristic
inferred from DOI database lookup
Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum
1 reference
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7 January 2021
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Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
1 reference
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Familial cases presenting very early onset autosomal dominant Alzheimer's disease with I143T in presenilin-1 gene: implication for genotype-phenotype correlation
1 reference
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7 January 2021
based on heuristic
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Mechanism of amyloid removal in patients with Alzheimer disease treated with gantenerumab.
1 reference
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Crossref
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https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
inferred from DOI database lookup
A mutant PSEN1 causes dementia with Lewy bodies and variant Alzheimer's disease.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
inferred from DOI database lookup
The value of PET in mild cognitive impairment, typical and atypical/unclear dementias: A retrospective memory clinic study
1 reference
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Crossref
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https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
inferred from DOI database lookup
Three postulates to help identify the cause of Alzheimer's disease
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations
1 reference
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reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
inferred from DOI database lookup
Familial Alzheimer disease: decreases in CSF Abeta42 levels precede cognitive decline.
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
A novel presenilin-1 mutation (Leu85Pro) in early-onset Alzheimer disease with spastic paraparesis.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
inferred from DOI database lookup
Toward defining the preclinical stages of Alzheimer's disease: recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease
1 reference
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reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
inferred from DOI database lookup
APOE and other loci affect age-at-onset in Alzheimer's disease families with PS2 mutation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): I--A review of clinical, radiologic and genetic aspects
1 reference
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https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotypic heterogeneity in familial Alzheimer's disease: a study of 24 kindreds
1 reference
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Crossref
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https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
inferred from DOI database lookup
Candidate gene for the chromosome 1 familial Alzheimer's disease locus
1 reference
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https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
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Pathology of early-onset Alzheimer's disease cases bearing the Thr113-114ins presenilin-1 mutation
1 reference
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Crossref
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https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
inferred from DOI database lookup
APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy
1 reference
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Crossref
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https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
inferred from DOI database lookup
Amyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Age at onset of Alzheimer's disease: relation to pattern of cognitive dysfunction and rate of decline
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
inferred from DOI database lookup
Very early-onset familial Alzheimer's disease: a novel presenilin 1 mutation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Age of onset in familial early onset Alzheimer's disease correlates with genetic aetiology.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Presentation of amyloidosis in carriers of the codon 692 mutation in the amyloid precursor protein gene (APP692).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Early onset familial Alzheimer's disease: Mutation frequency in 31 families.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The diagnosis of mild cognitive impairment due to Alzheimer's disease: recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
New V272A presenilin 1 mutation with very early onset subcortical dementia and parkinsonism.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
inferred from DOI database lookup
Early-versus late-onset Alzheimer's disease: more than age alone
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
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7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical phenotypic heterogeneity of Alzheimer's disease associated with mutations of the presenilin-1 gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A portrait of Alzheimer secretases--new features and familiar faces
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotype associated with APP duplication in five families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The diagnosis of dementia due to Alzheimer's disease: recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and neuropathological features of the arctic APP gene mutation causing early-onset Alzheimer disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Variations in the neuropathology of familial Alzheimer's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical features and APOE genotype of pathologically proven early-onset Alzheimer disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Early onset familial Alzheimer Disease with spastic paraparesis, dysarthria, and seizures and N135S mutation in PSEN1.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Why do DNA testing? Practical and ethical implications of new neurogenetic tests
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Carbon 11-labeled pittsburgh compound B positron emission tomographic amyloid imaging in patients with APP locus duplication
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The impact of different presenilin 1 andpresenilin 2 mutations on amyloid deposition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain: evidence for other phenotype-modifying factors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Behavioural-variant frontotemporal dementia: diagnosis, clinical staging, and management
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PICOGEN: five years experience with a genetic counselling program for dementia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The heritability and genetics of frontotemporal lobar degeneration.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diffusion tensor imaging in preclinical and presymptomatic carriers of familial Alzheimer's disease mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Amyloid vs FDG-PET in the differential diagnosis of AD and FTLD.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of risk genes on BOLD activation in presymptomatic carriers of familial Alzheimer's disease mutations during a novelty encoding task.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic counseling for early-onset familial Alzheimer disease in large Aboriginal kindred from a remote community in British Columbia: unique challenges and possible solutions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alzheimer's disease: clinical trials and drug development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Early-onset Alzheimer disease: when is genetic testing appropriate?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Report of the task force on designing clinical trials in early (predementia) AD.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Presymptomatic hippocampal atrophy in Alzheimer's disease. A longitudinal MRI study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pre-dementia clinical stages in presenilin 1 E280A familial early-onset Alzheimer's disease: a retrospective cohort study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The diagnosis of young-onset dementia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial Alzheimer's disease. A pedigree with a mis-sense mutation in the amyloid precursor protein gene (amyloid precursor protein 717 valine-->glycine).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A locus for familial early-onset Alzheimer's disease on the long arm of chromosome 14, proximal to the alpha 1-antichymotrypsin gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alzheimer's disease phenotypes and genotypes associated with mutations in presenilin 2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical-genetic correlations in familial Alzheimer's disease caused by presenilin 1 mutations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hemorrhage is uncommon in new Alzheimer family with Flemish amyloid precursor protein mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Whole genome analysis in a consanguineous family with early onset Alzheimer's disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The phenotypic spectrum of CADASIL: clinical findings in 102 cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Very early onset Alzheimer's disease with spastic paraparesis associated with a novel presenilin 1 mutation (Phe237Ile).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100013949
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1017/S0317167100013949
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22728850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
PubMed publication ID
22728850
1 reference
stated in
Europe PubMed Central
PubMed publication ID
22728850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 February 2020
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