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English
Molecular genetics of amyloid neuropathy in Europe
scientific article published on 01 March 1989
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
title
Molecular genetics of amyloid neuropathy in Europe
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
main subject
molecular genetics
1 reference
based on heuristic
inferred from title
amyloid neuropathy
1 reference
based on heuristic
inferred from title
author
Ian Holt
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
author name string
A E Harding
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
L Middleton
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
G Chrysostomou
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
G Said
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
R H King
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
P K Thomas
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
language of work or name
English
0 references
publication date
1 March 1989
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
volume
1
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
issue
8637
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
page(s)
524-526
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
cites work
A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990068-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990068-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990068-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of carriers of mutant prealbumin gene associated with familial amyloidotic polyneuropathy type I by Southern blot procedures: study of six pedigrees in the Arao district of Japan
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990068-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inherited predisposition to generalized amyloidosis. Clinical and pathological study of a family with neuropathy, nephropathy, and peptic ulcer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990068-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990068-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Revised analysis of amino acid replacement in a prealbumin variant (SKO-III) associated with familial amyloidotic polyneuropathy of Jewish origin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990068-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990068-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990068-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990068-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polyneuritic amyloidosis in a Japanese family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990068-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990068-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular detection of carriers of hereditary amyloidosis in a Swedish-American family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990068-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Onset in the seventh decade and lack of symptoms in heterozygotes for the TTRMet30 mutation in hereditary amyloid neuropathy—type I (Portuguese, Andrade)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990068-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(89)90068-8
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
PubMed ID
2564060
1 reference
stated in
Europe PubMed Central
PubMed ID
2564060
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2564060%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
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