Results 211 to 220 of about 37,209 (255)

Anti-IL1 treatment in colchicine-resistant paediatric FMF patients: real life data from the HELIOS registry.

Rheumatology, 2020
OBJECTIVES FMF is a prototype of autoinflammatory diseases associated with excess IL1 production. Anti-IL1 treatments are the first-line alternatives in colchicine-resistant/intolerant FMF patients. We aimed to investigate the efficacy and safety of anti-
E. Sağ, F. Akal, E. Atalay, U. Akca, S. Demir, Dilara Demirel, E. D. Batu, Y. Bilginer, S. Ozen   +8 more
semanticscholar   +1 more source

Association of FMF-Related (MEFV) Point Mutations with Secondary and FMF Amyloidosis

Nephron Clinical Practice, 2004
<i>Background:</i> Familial Mediterranean fever (FMF) is the major cause of AA amyloidosis in Turkey. M694V mutation in MEFV gene was suggested to be associated with severe clinical features and amyloidosis of FMF. <i>Methods:</i> In this study, the frequencies of three FMF-related MEFV mutations (M694V, M680I and V726A) were ...
M Pamir, Atagunduz, Serhan, Tuglular, Gulcin, Kantarci, Emel, Akoglu, Haner, Direskeneli   +4 more
openaire   +2 more sources

EULAR/PReS endorsed recommendations for the management of familial Mediterranean fever (FMF): 2024 update.

Annals of the Rheumatic Diseases
OBJECTIVES Familial Mediterranean fever (FMF) is the most common monogenic autoinflammatory disease despite being a rare disease for many rheumatologists.
Seza Ozen, E. Sağ, Teresa Otón, A. Gül, C. Sieiro Santos, Deniz Bayraktar, F. Proft, Helen J. Lachmann, Jasmin Kuemmerle Deschner, Marco Gattorno, Ömer Karadağ, Sezin Yüce, Shaye Kivity, Sophie Georgin-Lavialle, Tamara Sarkisian, T. Kallinich, V. Hentgen, Yeliz Prior, Y. Uziel, Ziv Yardeni, L. Carmona   +20 more
semanticscholar   +1 more source

Febbre Mediterranea Familiare (FMF)

Acta geneticae medicae et gemellologiae, 1960
RiassuntoNell'articolo vengono esposte le nostre osservazioni a proposito della FMF in base alle quali abbiamo inquadrato una nuova entità nosologica.Applicando dei criteri diagnostici definiti (a - attacchi febbrili ricorrenti accompagnati da b - dolori addominali, toracici o articolari) escludendo fattori causali noti, abbiamo diagnosticato la ...
Ezra Sohar, Mordechai Pras, Joram Heller, Joseph Gafni, Harry Heller   +4 more
openaire   +1 more source

High-order mode lasing in all-FMF laser cavities

Photonics Research, 2018
We experimentally demonstrate two kinds of all few-mode fiber (FMF) ring lasers with high-order mode (HOM) oscillation in the laser cavity. One kind is a switchable-wavelength all-FMF HOM laser with an output of tunable optical vortex beams (OVBs); the ...
Teng Wang, Ao Yang, Fan Shi, Yiping Huang, J. Wen, Xianglong Zeng   +5 more
semanticscholar   +1 more source

Familiäres Mittelmeerfieber (FMF)

2010
Das familiare Mittelmeerfieber ist eine autosomal rezessiv vererbte Erkrankung, die vor allem bei Menschen aus dem ostlichen Mittelmeer vorkommt. Das FMF ist gekennzeichnet durch meist in unregelmasigen Abstanden auftretende Fieberattacken ohne erkennbare Ursache, einhergehend mit Arthritis, Peritonitis und/oder seltener Pleuritis.
openaire   +1 more source

Old paradigms and new concepts in familial Mediterranean fever (FMF) - an update 2023.

Rheumatology, 2023
E. Ben-Chetrit
semanticscholar   +1 more source

Neurospora fmf-1: lure and lore

Journal of Genetics
The Neurospora crassa fmf-1 mutant has a unique phenotype. It arrests sexual development when the fruiting bodies (perithecia) attain only 40% of their normal diameter, regardless of whether the mutant participates in a cross with the wild type (fmf-1 x fmf-1+) as the male or female parent.
openaire   +2 more sources

Familial Mediterranean Fever (FMF)

2014
Familial Mediterranean Fever (FMF) is an autosomal recessive genetic disease that affects males and females. FMF gene is on the short arm of chromosome 16. It is most often found in Jews, Arabs, Turks, and Armenians. Amyloidosis is charecterized by the deposition of a particular protein between the cells in the tissue.
ALBAYRAK, Onur, ÇÜRÜK, M. Akif
openaire   +1 more source

[Amyloidosis of familial Mediterranean fever (FMF)--insights to FMF phenotype II].

Harefuah, 2007
Amyloidosis is the most grievous manifestation of Familial Mediterranean Fever (FMF), occurring in a high proportion of untreated patients. Continuously elevated serum amyloid A (SAA) levels during remissions, rather than a pulsatile rise during FMF attacks, underlies the development of amyloidosis.
openaire   +1 more source