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English
Inherited amyloidosis
scientific article published on February 1, 1991
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1016771
retrieved
18 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Inherited amyloidosis
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1016771
retrieved
18 August 2017
main subject
genetics
1 reference
stated in
Crossref
DOI
10.1136/JMG.28.2.73
reference URL
https://api.crossref.org/works/10.1136/JMG.28.2.73
retrieved
8 December 2022
author name string
M. D. Benson
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
1848299
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1848299
retrieved
8 December 2022
language of work or name
English
0 references
publication date
1 February 1991
1 reference
stated in
Europe PubMed Central
PMCID
1016771
retrieved
18 August 2017
full work available at URL
https://europepmc.org/articles/PMC1016771
file format
HTML
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed ID
1848299
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1848299
retrieved
8 December 2022
https://europepmc.org/articles/PMC1016771?pdf=render
file format
Portable Document Format
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed ID
1848299
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1848299
retrieved
8 December 2022
https://syndication.highwire.org/content/doi/10.1136/jmg.28.2.73
1 reference
stated in
Crossref
DOI
10.1136/JMG.28.2.73
reference URL
https://api.crossref.org/works/10.1136/JMG.28.2.73
retrieved
8 December 2022
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1016771
retrieved
18 August 2017
volume
28
1 reference
stated in
Europe PubMed Central
PMCID
1016771
retrieved
18 August 2017
page(s)
73-78
1 reference
stated in
Europe PubMed Central
PMCID
1016771
retrieved
18 August 2017
issue
2
1 reference
stated in
Europe PubMed Central
PMCID
1016771
retrieved
18 August 2017
cites work
A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016771
retrieved
6 September 2017
Variant apolipoprotein AI as a major constituent of a human hereditary amyloid
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016771
retrieved
6 September 2017
Plasma and cytoplasmic gelsolins are encoded by a single gene and contain a duplicated actin-binding domain
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016771
retrieved
6 September 2017
Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. A previously unrecognized heritable syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016771
retrieved
27 June 2018
Inherited predisposition to generalized amyloidosis. Clinical and pathological study of a family with neuropathy, nephropathy, and peptic ulcer
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016771
retrieved
27 June 2018
Familial primary amyloidosis with severe amyloid heart disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1848299
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1848299
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A new mutation causing familial amyloidotic polyneuropathy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1848299
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A novel variant of transthyretin (Tyr114 to Cys) deduced from the nucleotide sequences of gene fragments from familial amyloidotic polyneuropathy in Japanese sibling cases
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1848299
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Hereditary amyloidosis: detection of variant prealbumin genes by restriction enzyme analysis of amplified genomic DNA sequences
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1848299
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Finnish hereditary amyloidosis. Amino acid sequence homology between the amyloid fibril protein and human plasma gelsoline
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1848299
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Direct sequencing of the gene for Maryland/German familial amyloidotic polyneuropathy type II and genotyping by allele-specific enzymatic amplification
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1848299
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.28.2.73
1 reference
stated in
Europe PubMed Central
PMCID
1016771
retrieved
18 August 2017
PMCID
1016771
1 reference
stated in
Europe PubMed Central
PMCID
1016771
retrieved
18 August 2017
PubMed ID
1848299
1 reference
stated in
Europe PubMed Central
PMCID
1016771
retrieved
18 August 2017
ResearchGate publication ID
21308283
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