Results 11 to 20 of about 13,326 (150)

Bases genètiques de la febre mediterrània familiar a la població espanyola, dinàmica genòmica i història natural de les mutacions al locus "MEFV" [PDF]

open access: yes, 2004
[cat] La febre mediterrània familiar (FMF) afecta unes 10.000 i 100.000 persones d'origen principalment àrab, armeni, turc i jueu i és caracteritza per la recurrència d'episodis autolimitats de febre i inflamació de seroses, sense una causa infecciosa ...
Aldea Tomé, Anna
core   +6 more sources

Awareness of FMF among Caregivers [PDF]

open access: yes, 2021
Aim:Familial Mediterranean Fever (FMF) is one of the most frequent genetic diseases with a frequency of 1/1,000 in our country. We aimed to assess awareness of FMF among caregivers of patients with and without FMF.Materials and Methods:Caregivers of FMF ...
Belde Kasap Demir   +3 more
core   +1 more source

Familial Mediterranean Fever (FMF) in Turkey Results of a Nationwide Multicenter Study

open access: yes, 2005
: Familial Mediterranean fever (FMF) is an autosomal recessive disease that is prevalent among eastern Mediterranean populations, mainly non-Ashkenazi Jews, Armenians, Turks, and Arabs.
Turkish FMF Study Group*
core   +4 more sources

Comparison of Clinical and Demographic Features of FMF with Sacroiliitis Patients with FMF and Axial Spondyloarthritis Patients

open access: yes, 2021
© 2020 American Medical Association. All rights reserved.Zusammenfassung Ziele Familiäres Mittelmeerfieber (FMF) ist die haüfigste autoinflammatorische Erkrankung, die sich durch wiederholte, 1-3 Tage andauernde Fieber-und Serositisanfälle auszeichnet ...
ERSOY, OSMAN   +3 more
core   +1 more source

Family case with Familial Mediterranean fever (FMF) [PDF]

open access: yes, 2020
Background. Familial Mediterranean fever (FMF) is an auto-inflammatory disease characterized by periodic episodes of fever and recurrent polyserositis.
Rabia, Abed
core   +3 more sources

A large pericardial effusion and bilateral pleural effusions as the initial manifestations of Familial Mediterranean Fever [PDF]

open access: yes, 2015
Familial Mediterranean Fever (FMF) is a condition characterized by recurrent febrile poly-serositis. Typical presentations of the disease include episodes of fever, abdominal pain and joint pains. Chest pain is a less common presentation.
Mallia, Carmel   +4 more
core  

Association of FMF-Related (MEFV) point mutations with secondary and FMF amyloidosis

open access: yes, 2004
Background: 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.
DİRESKENELİ, RAFİ HANER   +1 more
core   +1 more source

Enhancement of the Plant‐Accessible Phosphate Fraction in Sewage Sludge Ashes by Na+ or K+ Addition Prior to Combustion

open access: yesChemSusChem, Volume 18, Issue 6, March 15, 2025.
The addition of Na2CO3 or K2CO3 to sewage sludge prior to combustion leads to the production of ashes containing phosphate in the form of buchwaldite‐like phases (Ca(Na/K)PO4). Compared to conventional sewage sludge mono‐ashes, such Na‐ or K‐ashes show greatly increased P‐solubilities and proved to be potent P‐fertiliser materials in greenhouse ...
Lorenz Bier‐Schorr   +4 more
wiley   +1 more source

A Bridged Copper(I) Diiodine Complex

open access: yesEuropean Journal of Inorganic Chemistry, EarlyView.
Bridging diiodine, high potentials: The bridged Cu(I) diiodine complex [(μ‐I2){Cu[Al(ORF)4]}2] forms by reacting the weakly coordinated dinitrogen complex [(N2)Cu{Al(ORF)4}] with I2. With very short Cu─I contacts and an elongated I─I bond, [(μ‐I2){Cu[Al(ORF)4]}2] is structurally predisposed to form CuI while oxidizing the weakly coordinating [Al(ORF)4]−
Julie Willrett   +2 more
wiley   +1 more source

Polyarteritis nodosa in patients with Familial Mediterranean fever (FMF): A concomitant disease or a feature of FMF?

open access: yes, 2001
Background: Familial Mediterranean fever (FMF) is caused by mutations in the gene encoding pyrin and is characterized by self-limited, recurrent attacks of fever and serositis.
Akpolat, I   +11 more
core   +1 more source

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