Results 121 to 130 of about 33,369 (222)

Type I IFN-mediated regulation of IL-1 production in inflammatory disorders [PDF]

open access: yes, 2018
Although contributing to inflammatory responses and to the development of certain autoimmune pathologies, type I interferons (IFNs) are used for the treatment of viral, malignant, and even inflammatory diseases.
Du Pasquier, Renaud   +3 more
core  

Mediterranean Fever gene analysis in the azeri turk population with familial mediterranean Fever: evidence for new mutations associated with disease.

open access: yesCell journal, 2013
Familial Mediterranean fever (FMF) is an autosomal recessive disorder characterized by recurrent febrile attacks accompanied by serosal and synovial membrane inflammation. FMF is caused by mutations in the MEFV gene and are found usually among Mediterranean populations, Armenians, Turks, Arabs and Jews.
Safar Farajnia, Leila Mohammadnejad
openaire   +2 more sources

Poster Session 3

open access: yes
Pregnancy, Volume 2, Issue S1, January 2026.
wiley   +1 more source

Relationship of Tel Hashomer criteria and Mediterranean fever gene mutations in a cohort of Turkish familial Mediterranean fever patients.

open access: yesSaudi medical journal, 2007
To evaluate the frequency of 5 mutations and their relationship with the Tel Hashomer criteria in 85 FMF patients.We looked for mutations in the Mediterranean fever (MEFV) gene in 84 consecutive patients who admitted to the Department of Medical Genetics of Afyon Kocatepe University, with a variable (from high to low) clinical suspicion of FMF.
Hale, Samli   +5 more
openaire   +1 more source

Diagnostic dilemma in autoinflammatory disease in two patients: does the name matter?

open access: yesThe Turkish Journal of Pediatrics, 2013
The systemic autoinflammatory diseases are inflammatory disorders characterized by uncontrolled inflammation of the innate immune system. A common monogenic autoinflammatory disease is familial Mediterranean fever (FMF), associated with mutations ...
Bora Gülhan   +3 more
doaj  

Complex MEFV and MVK Variations in a Syrian Child: Implications for Clinical Phenotypes and Treatment Response—A Case Report

open access: yesJournal of Investigative Medicine High Impact Case Reports
This case report presents a 10-year-old Syrian boy with concurrent mutations in the Mediterranean fever ( MEFV ) and mevalonate kinase ( MVK ) genes, resulting in overlapping symptoms of Familial Mediterranean Fever (FMF) and Hyperimmunoglobulinemia D ...
Alyamama Kousa MD   +4 more
doaj   +1 more source

Ricerca di Rickettsia del gruppo "Spotted Fever" in zecche antropofile raccolte in Toscana e Liguria [PDF]

open access: yes, 2012
Several tick-borne rickettsiae cause human diseases and, in the last years, the increased use of molecular-based identification methods has resulted in new spotted fever group rickettsiae being characterized in ixodid ticks throughout Europe.
FICHI, GIANLUCA
core  

Inflammatory osteolysis: A conspiracy against bone [PDF]

open access: yes, 2017
Abu-Amer   +36 more
core   +2 more sources

Updates on the role of epigenetics in familial mediterranean fever (FMF)

open access: yesOrphanet Journal of Rare Diseases
Familial Mediterranean Fever (FMF) is an autosomal recessive autoinflammatory disease caused by mutations in the MEFV (MEditerranean FeVer) gene that affects people originating from the Mediterranean Sea.
Ahlam Chaaban   +4 more
doaj   +1 more source

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