(Q37113817)

18 August 2017

1 reference

title

Autoinflammatory diseases: mimics of autoimmunity or part of its spectrum? Case presentation (English)

1 reference

18 August 2017

Maria Helena B Kiss

1

1 reference

18 August 2017

Claudia Saad Magalhães

series ordinal

2

1 reference

18 August 2017

publication date

20 March 2008

1 reference

Journal of Clinical Immunology

18 August 2017

published in

1 reference

18 August 2017

volume

28 Suppl 1

1 reference

18 August 2017

page(s)

S84-9

1 reference

https://scigraph.springernature.com/pub.10.1007/s10875-008-9179-2

18 August 2017

exact match

0 references

cites work

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

1 reference

12 December 2020

Myocarditis and sacroiliitis: 2 previously unrecognized manifestations of tumor necrosis factor receptor associated periodic syndrome

1 reference

12 December 2020

Chronic recurrent multifocal osteomyelitis associated with Crohn's disease

1 reference

12 December 2020

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

12 December 2020

Granulomatous nephritis associated with R334Q mutation in NOD2

1 reference

12 December 2020

A cryopyrin-associated periodic syndrome with joint destruction.

1 reference

12 December 2020

Clinical and genetic heterogeneity among Spanish patients with recurrent autoinflammatory syndromes associated with the CIAS1/PYPAF1/NALP3 gene.

1 reference

12 December 2020

Familial arthropathy with rash, uveitis and mental retardation

1 reference

12 December 2020

MEFV gene is a probable susceptibility gene for Behçet's disease

1 reference

12 December 2020

Pustulosis Palmoplantaris and Its Relation to Chronic Recurrent Multifocal Osteomyelitis

1 reference

12 December 2020

Conundrums in nosology: Synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome and spondylarthritis

1 reference

12 December 2020

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

1 reference

12 December 2020

Intrafamilial variable phenotypic expression of a CIAS1 mutation: from Muckle-Wells to chronic infantile neurological cutaneous and articular syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Arthropathy with rash, chronic meningitis, eye lesions, and mental retardation

1 reference

12 December 2020

Infantile multisystem inflammatory disease: a specific syndrome?

1 reference

12 December 2020

Familial Mediterranean fever and the other autoinflammatory syndromes: evaluation of the patient with recurrent fever.

1 reference

12 December 2020

Chronic inflammation: importance of NOD2 and NALP3 in interleukin-1beta generation

1 reference

12 December 2020

Autoinflammatory gene mutations in Behçet's disease

1 reference

12 December 2020

Autoinflammatory bone disorders

1 reference

12 December 2020

Chronic infantile neurological cutaneous and articular syndrome--an early description

1 reference

12 December 2020

Common FMF alleles may predispose to development of Behcet's disease with increased risk for venous thrombosis.

1 reference

12 December 2020

10.1007/S10875-008-9179-2

Identifiers

DOI

1 reference

18 August 2017

1 reference