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Is inadequate family history a barrier to diagnosis in CADASIL?
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16218915
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16218915%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
title
Is inadequate family history a barrier to diagnosis in CADASIL?
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16218915
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16218915%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
author
Keith Muir
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16218915
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16218915%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
author name string
Razvi SS
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16218915
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16218915%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
Davidson R
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16218915
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16218915%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
Bone I
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16218915
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16218915%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
language of work or name
English
0 references
publication date
1 November 2005
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16218915
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16218915%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
published in
Acta Neurologica Scandinavica
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16218915
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16218915%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
volume
112
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16218915
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16218915%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
issue
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16218915
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16218915%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
page(s)
323-326
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16218915
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16218915%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
cites work
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00495.X
retrieved
21 January 2018
Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00495.X
retrieved
21 January 2018
Long-term prognosis and causes of death in CADASIL: a retrospective study in 411 patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00495.X
retrieved
21 January 2018
The prevalence of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) in the west of Scotland
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00495.X
retrieved
21 January 2018
De novo mutation in the Notch3 gene causing CADASIL
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00495.X
retrieved
21 January 2018
Identifiers
DOI
10.1111/J.1600-0404.2005.00495.X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16218915
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16218915%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
PubMed publication ID
16218915
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16218915
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16218915%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
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