TRIM family proteins and their emerging roles in innate immunity

K Ozato, DM Shin, TH Chang… - Nature reviews …, 2008 - nature.com
The superfamily of tripartite motif-containing (TRIM) proteins is conserved throughout the
metazoan kingdom and has expanded rapidly during vertebrate evolution; there are now …

[HTML][HTML] Familial Mediterranean fever: recent developments in pathogenesis and new recommendations for management

S Özen, ED Batu, S Demir - Frontiers in immunology, 2017 - frontiersin.org
Familial Mediterranean fever (FMF) is the most common monogenic autoinflammatory
disease (AID) affecting mainly the ethnic groups originating from Mediterranean basin. The …

[HTML][HTML] Familial Mediterranean fever—a review

M Shohat, GJ Halpern - Genetics in Medicine, 2011 - Elsevier
Familial Mediterranean fever is inherited in an autosomal recessive manner. There are two
phenotypes: types 1 and 2. Familial Mediterranean fever type 1 is characterized by recurrent …

As a new inflammatory marker for familial Mediterranean fever: neutrophil-to-lymphocyte ratio

A Ahsen, MS Ulu, S Yuksel, K Demir, M Uysal… - Inflammation, 2013 - Springer
Familial Mediterranean fever (FMF), which is an autosomal recessive disease, is
characterised by recurrent febrile episodes in association with peritonitis, pleuritis and …

Familial Mediterranean fever in childhood: a single-center experience

K Barut, S Sahin, A Adrovic, AB Sinoplu… - Rheumatology …, 2018 - Springer
The aim of this study is to present demographic and clinical features, MEFV mutation
variations, and treatment response of a large number of pediatric familial Mediterranean …

Familial Mediterranean fever in Japan

K Migita, R Uehara, Y Nakamura, M Yasunami… - Medicine, 2012 - journals.lww.com
Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disease that is
prevalent in Mediterranean populations. While it is considered a rare disease in the rest of …

[HTML][HTML] Familial Mediterranean fever is no longer a rare disease in Japan

K Migita, Y Izumi, Y Jiuchi, N Iwanaga… - Arthritis research & …, 2016 - Springer
Background The aim of this study was to evaluate the clinical manifestations and prevalence
of familial Mediterranean fever (FMF) in Japanese patients with unexplained fever and …

[HTML][HTML] Update on the management of colchicine resistant Familial Mediterranean Fever (FMF)

G El Hasbani, A Jawad, I Uthman - Orphanet journal of rare diseases, 2019 - Springer
Abstract Background Familial Mediterranean Fever (FMF), an autoinflammatory disease, is
characterized by self-limited inflammatory attacks of fever and polyserositis along with high …

Pediatric fever of unknown origin

JW Antoon, NM Potisek, JA Lohr - Pediatrics in review, 2015 - publications.aap.org
Pediatric Fever of Unknown Origin | Pediatrics In Review | American Academy of Pediatrics
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[HTML][HTML] Familial Mediterranean fever: assessing the overall clinical impact and formulating treatment plans

R Manna, D Rigante - Mediterranean journal of hematology and …, 2019 - ncbi.nlm.nih.gov
Recurrent self-limited attacks of fever and short-lived inflammation in the serosal
membranes, joints, and skin are the leading features of familial Mediterranean fever (FMF) …