An integrated classification of pediatric inflammatory diseases, based on the concepts of autoinflammation and the immunological disease continuum. (Q52850152)

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scientific article published in May 2009

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English	An integrated classification of pediatric inflammatory diseases, based on the concepts of autoinflammation and the immunological disease continuum.	scientific article published in May 2009

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scholarly article

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/19190531

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

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/19190531

1 reference

based on heuristic

inferred from title

Michael McDermott

4

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/19190531

Dennis McGonagle

1

object named as

Dennis McGonagle

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author name string

Azad Aziz

2

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/19190531

Laura J Dickie

3

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/19190531

language of work or name

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publication date

1 May 2009

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/19190531

Pediatric Research

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Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/19190531

65

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/19190531

5 Pt 2

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/19190531

38R-45R

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/19190531

https://scigraph.springernature.com/pub.10.1203/pdr.0b013e31819dbd0a

0 references

The hereditary autoinflammatory syndromes

1 reference

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21 January 2018

A proposed classification of the immunological diseases

1 reference

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The NLR network and the immunological disease continuum of adaptive and innate immune-mediated inflammation against self

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From inflammasomes to fevers, crystals and hypertension: how basic research explains inflammatory diseases

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

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Cryopyrinopathies: update on pathogenesis and treatment.

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Ancient Missense Mutations in a New Member of the RoRet Gene Family Are Likely to Cause Familial Mediterranean Fever

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A candidate gene for familial Mediterranean fever

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Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome

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Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group.

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Familial cold autoinflammatory syndrome: phenotype and genotype of an autosomal dominant periodic fever

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

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Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis

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Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder

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Pyrin binds the PSTPIP1/CD2BP1 protein, defining familial Mediterranean fever and PAPA syndrome as disorders in the same pathway

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A common pathway in periodic fever syndromes

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The clinical continuum of cryopyrinopathies: novel CIAS1 mutations in North American patients and a new cryopyrin model

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NALP3 forms an IL-1beta-processing inflammasome with increased activity in Muckle-Wells autoinflammatory disorder

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Familial autoinflammatory diseases: genetics, pathogenesis and treatment

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Autoinflammatory genes and susceptibility to psoriatic juvenile idiopathic arthritis

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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

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A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

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CARD15 mutations in Blau syndrome

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Presence of a sporadic case of systemic granulomatosis syndrome with a CARD15 mutation.

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The importance of 'Mechnikov's thorn' for an improved understanding of 21st century medicine and immunology: a view from the eye.

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Mutation of mouse Mayp/Pstpip2 causes a macrophage autoinflammatory disease.

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Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease

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T cells and cytokines in Crohn's disease

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New links to the pathogenesis of Crohn disease provided by genome-wide association scans

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Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease

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Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility

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Differential activity of IL-12 and IL-23 in mucosal and systemic innate immune pathology.

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A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1

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Treatment of murine colitis by Lactococcus lactis secreting interleukin-10.

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Increased frequency of mutations in the gene responsible for familial Mediterranean fever (MEFV) in a cohort of patients with ulcerative colitis: evidence for a potential disease-modifying effect?

1 reference

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The familial Mediterranean fever (MEFV) gene may be a modifier factor of inflammatory bowel disease in infancy.

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MEFV mutations in Behçet's disease

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The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

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Positional cloning of the APECED gene

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Autoantibodies against Type I Interferons as an Additional Diagnostic Criterion for Autoimmune Polyendocrine Syndrome Type I

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Genetics of autoimmune diseases--disorders of immune homeostasis

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STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus

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Newly identified genetic risk variants for celiac disease related to the immune response

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The inflammatory disease-associated variants in IL12B and IL23R are not associated with rheumatoid arthritis

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Successful treatment of acute visual loss in Muckle-Wells syndrome with interleukin 1 receptor antagonist

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Lasting remission of a Muckle-Wells syndrome with CIAS-1 mutation using half-dose anakinra.

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Spectrum of clinical features in Muckle-Wells syndrome and response to anakinra

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New CIAS1 mutation and anakinra efficacy in overlapping of Muckle-Wells and familial cold autoinflammatory syndromes

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Interleukin-1 blockade by anakinra improves clinical symptoms in patients with neonatal-onset multisystem inflammatory disease

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A pilot study to evaluate the safety and efficacy of the long-acting interleukin-1 inhibitor rilonacept (interleukin-1 Trap) in patients with familial cold autoinflammatory syndrome

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Identifiers

10.1203/PDR.0B013E31819DBD0A

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/19190531

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0 references

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/19190531

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