authors
- Yikilmaz, Ali
- Gunduz, Zubeyde
- Dursun, Ismail
- Aróstegui, Juan I
- Yagüe, Jordi
- Dusunsel, Ruhan
- Poyrazoglu, Hakan M
- Gurgoze, Metin Kaya
- Yıkılmaz, Ali
A fatal turkish case of CINCA-NOMID syndrome due to the novel Val-351-Leu CIAS1 gene mutation
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Overview
status
publication date
- February 2008
has subject area
- 1103 Clinical Sciences (FoR)
- Adolescent (MeSH)
- Anti-Inflammatory Agents, Non-Steroidal (MeSH)
- Arthritis & Rheumatology (Science Metrix)
- Autoimmune Diseases (MeSH)
- Carrier Proteins (MeSH)
- Chronic Disease (MeSH)
- Etanercept (MeSH)
- Exons (MeSH)
- Fatal Outcome (MeSH)
- Genetic Predisposition to Disease (MeSH)
- Humans (MeSH)
- Immunoglobulin G (MeSH)
- Infant, Newborn (MeSH)
- Infant, Newborn, Diseases (MeSH)
- Inflammation (MeSH)
- Magnetic Resonance Imaging (MeSH)
- Male (MeSH)
- Mutation, Missense (MeSH)
- NLR Family, Pyrin Domain-Containing 3 Protein (MeSH)
- Phenotype (MeSH)
- Receptors, Tumor Necrosis Factor (MeSH)
- Risk Factors (MeSH)
- Syndrome (MeSH)
- Treatment Outcome (MeSH)
- Turkey (MeSH)
published in
- Rheumatology International Journal