De novoCIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): A new member of the expanding family of pyrin-associated autoinflammatory diseases-Reference-Cited by-同舟云学术

De novoCIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): A new member of the expanding family of pyrin-associated autoinflammatory diseases

Published:2002-12 Issue:12 Volume:46 Page:3340-3348
ISSN:0004-3591
Container-title:Arthritis & Rheumatism
language:en
Short-container-title:Arthritis & Rheumatism

Author:

Aksentijevich Ivona,Nowak Miroslawa,Mallah Mustapha,Chae Jae Jin,Watford Wendy T.,Hofmann Sigrun R.,Stein Leonard,Russo Ricardo,Goldsmith Donald,Dent Peter,Rosenberg Helene F.,Austin Frances,Remmers Elaine F.,Balow James E.,Rosenzweig Sergio,Komarow Hirsh,Shoham Nitza G.,Wood Geryl,Jones Janet,Mangra Nadira,Carrero Hector,Adams Barbara S.,Moore Terry L.,Schikler Kenneth,Hoffman Hal,Lovell Daniel J.,Lipnick Robert,Barron Karyl,O'Shea John J.,Kastner Daniel L.,Goldbach-Mansky Raphaela

Publisher

Wiley

Subject

Pharmacology (medical),Immunology,Rheumatology,Immunology and Allergy

Reference45 articles.

1. Germline Mutations in the Extracellular Domains of the 55 kDa TNF Receptor, TNFR1, Define a Family of Dominantly Inherited Autoinflammatory Syndromes

2. TNFRSF1A mutations and autoinflammatory syndromes

3. A fever gene comes in from the cold

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

5. A candidate gene for familial Mediterranean fever

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