(Q38496586)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25998913%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

review article

1 reference

title

The autoinflammatory diseases: a fashion with blurred boundaries! (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25998913%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25998913%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

Isabelle Touitou

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25998913%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

author name string

M Barat-Houari

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25998913%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

S Annakib

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25998913%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

publication date

22 May 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25998913%20AND%20SRC:MED&resulttype=core&format=json

Seminars in Immunopathology

8 March 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25998913%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

volume

37

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25998913%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25998913%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

page(s)

359-362

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25998913%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00281-015-0495-3

8 March 2020

exact match

0 references

cites work

Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes.

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

The infevers autoinflammatory mutation online registry: update with new genes and functions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

INFEVERS: the Registry for FMF and hereditary inflammatory disorders mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Infevers: an evolving mutation database for auto-inflammatory syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

An integrated classification of pediatric inflammatory diseases, based on the concepts of autoinflammation and the immunological disease continuum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

An activating NLRC4 inflammasome mutation causes autoinflammation with recurrent macrophage activation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

The inflammasome: a molecular platform triggering activation of inflammatory caspases and processing of proIL-beta

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Use of canakinumab in the cryopyrin-associated periodic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Genetic analysis as a valuable key to diagnosis and treatment of periodic Fever

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Clinical impact of MEFV mutations in children with periodic fever in a prevalent western European Caucasian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Familial Mediterranean fever in heterozygotes: are we able to accurately diagnose the disease in very young children?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Treatment of autoinflammatory diseases: results from the Eurofever Registry and a literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Mevalonate kinase deficiencies: from mevalonic aciduria to hyperimmunoglobulinemia D syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Mutations in the mevalonate kinase (MVK) gene cause nonsyndromic retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Exome sequencing identifies MVK mutations in disseminated superficial actinic porokeratosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Genetics of monogenic autoinflammatory diseases: past successes, future challenges

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Activated STING in a vascular and pulmonary syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00281-015-0495-3

Myeloid lineage-restricted somatic mosaicism of NLRP3 mutations in patients with variant Schnitzler syndrome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25998913

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Autoinflammatory response to self-antigens of lymphoblasts

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25998913