Elevated systemic antibodies towards commensal gut microbiota in autoinflammatory condition [PDF]
, 2008 Article No.
Aminov, Rustam I +7 more
core +11 more sources
BMC Medical Genetics, 2017 Background Familial Mediterranean fever is an autosomal recessive disease characterized by recurrent episodes of fever and polyserositis and by the onset of reactive amyloid-associated amyloidosis. Amyloidosis due to familial Mediterranean fever can lead
Ramón Peces +4 more
doaj +1 more source
High prevalence of Rickettsia africae variants in Amblyomma variegatum ticks from domestic mammals in rural western Kenya: implications for human health [PDF]
, 2014 Tick-borne spotted fever group (SFG) rickettsioses are emerging human diseases caused by obligate intracellular Gram-negative bacteria of the genus Rickettsia.
Ade, Fredrick +13 more
core +3 more sources
Familial Mediterranean fever : MEFV gene mutations and treatment
Japanese Journal of Clinical Immunology, 2007 Familial Mediterranean fever (FMF) is an autosomal recessive disease which predominantly affects certain ethnic groups mainly Sephardic Jews, Turks, Arabs and Armenians. FMF has been rarely reported in Japan. Characteristic symptoms include self-limited recurrent attacks of fever with serositis such as peritonitis, pleuritis, and arthritis.
Megumu, Saito +2 more
openaire +3 more sources
Dolphin Morbillivirus in Eurasian Otters, Italy [PDF]
, 2019 We report biomolecular evidence of dolphin morbillivirus in 4 wild Eurasian otters (Lutra lutra) from southern Italy; 2 animals showed simultaneous immunohistochemical reactivity against morbilliviral antigen.
Cafiero, Maria Assunta +13 more
core +1 more source
Vertebral artery dissection associated with familial Mediterranean fever and Behçet's disease
Annals of Clinical and Translational Neurology, 2019 Vertebral artery dissection and recurrent meningitis are rare complications in Behçet's disease. Behçet's disease may be associated with familial Mediterranean fever.
Hidehiro Ishikawa +9 more
doaj +1 more source
SIMILARITIES AND DIFFERENCES BETWEEN FAMILIAL MEDITERRANEAN FEVER AND BEHÇET’S DISEASE
Central Asian Journal of Medical Hypotheses and Ethics, 2021 Familial Mediterranean Fever (FMF) is the most common monogenic autoinflammatory disease, mainly affecting populations originating from the Eastern Mediterranean region. Behçet’s Disease (BD) is grouped in polygenic autoinflammatory diseases.
Ummusen Kaya Akca, Ezgi Deniz Batu
doaj +1 more source
Concurrent TNFRSF1A R92Q and pyrin E230K mutations in a child with multiple sclerosis [PDF]
, 2010 We report a 16-year-old female patient with a severe course of multiple sclerosis and concomitant symptoms suggestive of a hereditary autoinflammatory disease.
Blaschek, Astrid +7 more
core +1 more source
Cold Exposure Related Fever with an Mediterranean Fever (MEFV) Gene Mutation
Internal Medicine, 2017 Familial Mediterranean fever (FMF) is a genetic autoinflammatory disease characterized by recurrent fever with serosal inflammation. We experienced a 53-year-old male who had been suffering from periodic attacks with slight fever and myalgia which were mainly triggered by cold exposure in winter.
Kumei, Shima +4 more
openaire +3 more sources
Familial Mediterranean fever presenting as fever of unknown origin in Korea [PDF]
Korean Journal of Pediatrics, 2016 Familial Mediterranean fever (FMF) is the most common Mendelian autoinflammatory disease, characterized by uncontrolled activation of the innate immune system that manifests as recurrent brief fever and polyserositis (e.g., peritonitis, pleuritic, and ...
Jun Hee Lee +6 more
doaj +1 more source