(Q35019675)

5 August 2017

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title

Genetic clues to understanding periodic fevers, and possible therapies (English)

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5 August 2017

1

Michael F McDermott

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5 August 2017

1 December 2002

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Trends in Molecular Medicine

5 August 2017

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5 August 2017

8

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5 August 2017

12

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5 August 2017

550-554

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Hereditary periodic fever

5 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

A candidate gene for familial Mediterranean fever

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

The PYRIN domain: a member of the death domain-fold superfamily

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

PYPAF1, a PYRIN-containing Apaf1-like protein that assembles with ASC and regulates activation of NF-kappa B

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Interaction between pyrin and the apoptotic speck protein (ASC) modulates ASC-induced apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

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/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

The molecular architecture of the TNF superfamily

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

The pyrin domain: a possible member of the death domain-fold family implicated in apoptosis and inflammation

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

The tumor-necrosis-factor receptor-associated periodic syndrome: new mutations in TNFRSF1A, ancestral origins, genotype-phenotype studies, and evidence for further genetic heterogeneity of periodic fevers

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

MEFV mutations in Behçet's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

A single mutated MEFV allele in Israeli patients suffering from familial Mediterranean fever and Behçet's disease (FMF-BD).

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF).

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

The spectrum of Familial Mediterranean Fever (FMF) mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implications

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

The MICA region determines the first modifier locus in familial Mediterranean fever

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Autosomal-dominant periodic fever with AA amyloidosis: Novel mutation in tumor necrosis factor receptor 1 gene Rapid Communication

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Familial periodic fever and amyloidosis due to a new mutation in the TNFRSF1A gene

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

A novel mutation in the third extracellular domain of the tumor necrosis factor receptor 1 in a Finnish family with autosomal-dominant recurrent fever

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

An Israeli Arab patient with a de novo TNFRSF1A mutation causing tumor necrosis factor receptor-associated periodic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in a Dutch family: evidence for a TNFRSF1A mutation with reduced penetrance

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Mutational spectrum in the MEFV and TNFRSF1A genes in patients suffering from AA amyloidosis and recurrent inflammatory attacks

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

The enlarging clinical, genetic, and population spectrum of tumor necrosis factor receptor-associated periodic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Clinical and molecular variability in childhood periodic fever with hyperimmunoglobulinaemia D.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Molecular analysis of MVK mutations and enzymatic activity in hyper-IgD and periodic fever syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Identification of a locus on chromosome 1q44 for familial cold urticaria

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

An autosomal dominant periodic fever associated with AA amyloidosis in a north Indian family maps to distal chromosome 1q.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

The NACHT family - a new group of predicted NTPases implicated in apoptosis and MHC transcription activation

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

CARD15 mutations in Blau syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Defective LPS Signaling in C3H/HeJ and C57BL/10ScCr Mice: Mutations in Tlr4 Gene

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Relevance of mutations in the TLR4 receptor in patients with gram-negative septic shock

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Colchicine in the prevention and treatment of the amyloidosis of familial Mediterranean fever

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

TNFRSF1A mutations and autoinflammatory syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Treatment of the nephrotic syndrome with etanercept in patients with the tumor necrosis factor receptor-associated periodic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Hereditary periodic fever

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

New drugs for the treatment of rheumatoid arthritis

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Infliximab and methotrexate in the treatment of rheumatoid arthritis. Anti-Tumor Necrosis Factor Trial in Rheumatoid Arthritis with Concomitant Therapy Study Group

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Demyelination occurring during anti-tumor necrosis factor alpha therapy for inflammatory arthritides

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

Tuberculosis associated with infliximab, a tumor necrosis factor alpha-neutralizing agent

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902425-5

7 January 2021

10.1016/S1471-4914(02)02425-5

Identifiers

DOI

1 reference

5 August 2017

1 reference

PubMed ID

12470987