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English
The inherited autoinflammatory syndrome: a decade of discovery.
scientific article published on January 2009
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
2744542
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19768193%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 February 2020
review article
1 reference
stated in
Europe PubMed Central
title
The inherited autoinflammatory syndrome: a decade of discovery
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
2744542
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19768193%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 February 2020
author name string
Stephen Goldfinger
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
2744542
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19768193%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 February 2020
publication date
1 January 2009
1 reference
stated in
Europe PubMed Central
PMC publication ID
2744542
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19768193%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 February 2020
published in
Transactions of the American Clinical and Climatological Association
1 reference
stated in
Europe PubMed Central
PMC publication ID
2744542
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19768193%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 February 2020
volume
120
1 reference
stated in
Europe PubMed Central
PMC publication ID
2744542
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19768193%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 February 2020
page(s)
413-418
1 reference
stated in
Europe PubMed Central
PMC publication ID
2744542
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19768193%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 February 2020
cites work
Cryopyrinopathies: update on pathogenesis and treatment.
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=2744542
retrieved
23 August 2017
The clinical continuum of cryopyrinopathies: novel CIAS1 mutations in North American patients and a new cryopyrin model
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2744542
retrieved
23 August 2017
Urticaria, deafness, and amyloidosis: a new heredo-familial 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=2744542
retrieved
23 August 2017
The TNF receptor-associated periodic syndrome (TRAPS): emerging concepts of an autoinflammatory disorder
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=2744542
retrieved
23 August 2017
A recently recognised chronic inflammatory disease of early onset characterised by the triad of rash, central nervous system involvement and arthropathy
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=2744542
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23 August 2017
Spectrum of clinical features in Muckle-Wells syndrome and response to anakinra
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PubMed Central
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14 September 2017
Molecular analysis of the mevalonate kinase gene in a cohort of patients with the hyper-igd and periodic fever syndrome: its application as a diagnostic tool
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PubMed Central
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14 September 2017
Familial Mediterranean fever. A survey of 470 cases and review of the literature
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2744542
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14 September 2017
Hyperimmunoglobulinemia D and periodic fever syndrome. The clinical spectrum in a series of 50 patients. International Hyper-IgD Study Group
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PubMed Central
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28 September 2017
Colchicine therapy for familial mediterranean fever. A double-blind trial
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2744542
retrieved
28 September 2017
A New Autosomal Dominant Disorder of Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne: PAPA Syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/19768193
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Ancient Missense Mutations in a New Member of the RoRet Gene Family Are Likely to Cause Familial Mediterranean Fever
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/19768193
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Familial cold urticaria. Clinical findings
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/19768193
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
2744542
1 reference
stated in
Europe PubMed Central
PMC publication ID
2744542
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19768193%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 February 2020
PubMed publication ID
19768193
1 reference
stated in
Europe PubMed Central
PMC publication ID
2744542
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19768193%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 February 2020
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