Results 101 to 110 of about 846,391 (207)

Assessment of Interleukin-33 Levels in Patients with Familial Mediterranean Fever

Romanian Journal of Internal Medicine
This study was designed to evaluate the relationship between serum interleukin-33 (IL-33) levels and clinical features of the disease in patients with Familial Mediterranean Fever (FMF).
Demirezen Asil, Güler Aslihan Avanoğlu, Karadeniz Hazan, Kavutçu Mustafa, Tufan Abdurrahman   +4 more
doaj   +1 more source

Diagnostic yield of real-time PCR vs. NGS in pediatric FMF: insights from a Turkish cohort

Open Medicine
Familial Mediterranean Fever (FMF) is the most common monogenic autoinflammatory disease, especially in Mediterranean populations. This study compares the diagnostic value of real-time PCR and next-generation sequencing (NGS) in a Turkish pediatric ...
Göktaş Emine, Kurnaz Demir Tuğba Deniz, Zamani Ayşe Gül, Yildirim Mahmut Selman   +3 more
doaj   +1 more source

Sacroiliitis in familial Mediterranean fever: an unusual presentation in childhood

The Turkish Journal of Pediatrics, 1999
Familial Mediterranean fever (FMF) is an autosomal recessively transmitted disease characterized by attacks of fever and serositis. The course of arthritis, which is a common manifestation of FMF, is generally benign.
N Beşbaş, S Ozdemir, I Saatçi, A Bakkaloğlu, S Ozen, U Saatçi   +5 more
doaj  

Reactive Amyloidosis and Familial Mediterranean Fever (FMF)

Internal Medicine, 2002
TAKAHASHI, Naoki, SUZUKI, Eiichi, GEJYO, Fumitake   +2 more
openaire   +3 more sources

Canakinumab as rescue therapy in familial Mediterranean fever refractory to conventional treatment

, 2015
Mirella Alpa, Dario Roccatello Centro di Ricerche di Immunopatologia e Documentazione su Malattie Rare (CMID), Struttura Complessa Direzione Universitaria di Immunologia Clinica, Università di Torino e Ospedale G Bosco, Torino, ItalyAbstract ...
Alpa M, Roccatello D
core  

Lithium prophylaxis in familial Mediterranean fever

, 1979
Familial Mediterranean fever (FMF), also called familial paroxysmal polyserositis or periodic disease, is a heredo-familial disorder of recurrent course, peculiar ethnic distribution and unknown etiology.
Loukopoulos, D.L., Christodoulou, G.N., Madianos, M.G., Stefanis, C.N.   +3 more
core   +1 more source

Familial Mediterranean fever

, 2002
Background. The pathogenesis of familial Mediterranean fever (IMF) is unknown, and since no specific laboratory test is yet available, the diagnosis of FMF remains clinical.
Cetinkaya, R, Odabas, AR, Bilen, Habib, Selcuk, Y   +3 more
core  

Protracted Febrile Myalgia Syndrome: A Case Report Focusing on Possible Environmental Triggers

The Turkish Journal of Gastroenterology, 2013
Protracted febrile myalgia syndrome (PFMS) is an uncommon, dramatic manifestation of familial Mediterranean fever (FMF) which is characterized by severe myalgia and high fever. This syndrome is considered to be either a rare type of vasculitis requiring
Mahmut ALPAYCI, Arda KANDEMİR, Mehmet KORKMAZ2   +2 more
doaj  

Lack of the Association of the PTPN22 C1858T Gene Polymorphism With Susceptibility to Familial Mediterranean Fever

The Turkish Journal of Gastroenterology, 2016
Objectives: This study aims to investigate whether the protein tyrosine phosphatase non-receptor type 22 (PTPN22) C1858T gene polymorphism plays a role in the pathogenesis of familial Mediterranean fever (FMF) through T-lymphocyte activation ...
Orhan KÜÇÜKŞAHİN, Şükran ERTEN, Emre KÜLAHÇIOĞLU, Alexis K OKOH, Murat TURGAY, Timur TUNCALI, Gülay KINIKLI, Ali ŞAHİN, Zeynep ŞEKER, Aşkın ATEŞ   +9 more
doaj  

A Unique Complex Variation Profile in a Patient with Familial Mediterranean Fever (FMF): Triple Homozygous E148Q-P369S-R408Q - "Case Report". [PDF]

Appl Clin Genet
Abi Chakra N, Yazbeck N, Fattah MO, Hanna-Wakim R.   +3 more
europepmc   +1 more source