Makale detayı · 2014 · article
Familial Mediterranean fever An updated review
Veri kaynağı ayrımı
- YÖKSİSYÖKSİS makale kaydı
- YÖKSİS dergi adıEuropean Journal of Rheumatology
- OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
- Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)
Özet
Familial Mediterranean Fever (FMF) is a hereditary autoinflammatory disorder characterised by acute attacks of fever and serosal inflammation. FMF primarily affects Jewish, Armenian, Turkish, and Arab populations. The disease is accompanied by a marked decrease in quality of life due to the effects of attacks and subclinical inflammation in the attack-free periods. Untreated or inadequately treated patients run the risk of amyloidosis, which is an important cause of morbidity and mortality. In this review, the current information available on FMF is summarised.
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Yerel katalogda bu makaleye atıf yapan 180 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).
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- 2018 Comparison of early versus late onset familial Mediterranean feverAtıf 38 · OpenAlex