Results 31 to 40 of about 11,340 (243)
Serum Calprotectin in Children with Familial Mediterranean Fever [PDF]
Pediatric Sciences JournalBackground: Familial Mediterranean fever (FMF) is the most prevalent inherited autoinflammatory disease worldwide. Ongoing subclinical inflammation, induces amyloidosis, even during the attack-free periods despite colchicine therapy.
Huda Marzouk +3 more
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P01-003 – Bleeding disorder in FMF [PDF]
Pediatric Rheumatology, 2013 The most serious complication in Familial Mediterranean fever (FMF) is the development of amyloidosis, which usually determines the prognosis. Amyloid deposition can be systemic or organ-specific. The clinical features of amyloidosis are dependent on the organs involved, type of amyloidosis, rate of amyloid deposition and amount of amyloid fibrils ...
Karadag, O +3 more
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A Negative Correlation Between MEFV Mutations and Allergic Diseases
Journal of Pediatric Research, 2022 Aim:Atopy is associated with a genetic predisposition to develop allergic diseases such as allergic rhinitis, asthma, and atopic dermatitis. In this study, we aimed to compare the prevalence of Familial Mediterranean Fever (FMF) mutations in asthma and ...
Malik Ejder Yıldırım +3 more
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Evaluation of changes in liver functions during and after FMF attacks [PDF]
African Journal of Gastroenterology and HepatologyBackground: FMF is a recessive genetic condition associated with missense and nonsense mutations in the MEFV gene, located on the short arm of chromosome 16. The serous tissue of numerous organs is the primary target of FMF.
Ahmed Mohsen +3 more
doaj +1 more source
A Transcriptional Map of the FMF Region
Genomics, 1998 Familial Mediterranean fever (FMF) is a recessively inherited disorder characterized by attacks of fever and serositis, which affects primarily non-Ashkenazi Jews, Armenians, Turks, and Arabs. We present here a transcriptional map covering the FMF locus that we constructed in the course of the positional cloning of the gene responsible for this disease.
A, Bernot +14 more
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Nature Communications, 2019 Carbonyl complexes have been studied extensively thanks to their rich substitution and redox chemistry, but most homoleptic transition metal carbonyl complexes isolated in the condensed phase are neutral or anionic.
Jan Bohnenberger +5 more
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Familial Mediterranean Fever and Transverse Myelitis: A Causal Relation?
Neurology and Therapy, 2023 Familial Mediterranean fever (FMF) is a rare autoinflammatory disorder characterized mainly by recurrent self-limited episodes of fever and polyserositis.
Ali Motahharynia +4 more
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Response to requests by FMF and DWPF concerning disposal of FMF saltstone drums in Z-Area vaults [PDF]
, 1989 Disposal of FMF saltstone in 55 gallon drums in the Z-Area Industrial Waste Landfill requires modification of the landfill permit. Approximately 5000 drums of FMF saltstone are currently stored on SC DHEC-permitted concrete storage pads adjacent to the ...
Langton, C. A., Cook, J. R.
core +3 more sources
Abstract 26 — Clinical Characteristics of Familial Mediterranean: Fever in Hemodialysis Patients
Journal of Clinical Rheumatology and Immunology, 2023 Introduction Familial Mediterranean fever (FMF) is an inherited genetic disorder characterized by recurrent episodes of fever, serositis, arthritis, and skin rash. Uncontrolled disease can lead to amyloid A disposition, nephrotic syndrome and progressive
Fatima AlKindi +12 more
doaj +1 more source
FMF presented by aseptic abscesses
Ulusal Romatoloji Dergisi, 2023 A 23-year-old otherwise healthy female with family history of familial Mediterranean fever (FMF) in 2 siblings who are on colchicine presented with fever, pleuritis, pericarditis, peritonitis and multiple abscesses in the liver. Sampling from the liver abscess showed neutrophil predominance with no findings of granuloma, vasculitis, lymphoma or ...
Seyda Bilgin, Serdal Uğurlu
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