Results 231 to 240 of about 35,452 (278)
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Southern Medical Journal, 2002
The pathogenesis of familial Mediterranean fever (FMF) is unknown, and since no specific laboratory test is yet available, the diagnosis of FMF remains clinical. The purpose of this study was to review clinical characteristics of patients with FMF.A total of 96 patients with FMF were evaluated either retrospectively (for those diagnosed before 1997) or
Ali Riza, Odabas +3 more
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The pathogenesis of familial Mediterranean fever (FMF) is unknown, and since no specific laboratory test is yet available, the diagnosis of FMF remains clinical. The purpose of this study was to review clinical characteristics of patients with FMF.A total of 96 patients with FMF were evaluated either retrospectively (for those diagnosed before 1997) or
Ali Riza, Odabas +3 more
openaire +2 more sources
Update in familial Mediterranean fever
Current Opinion in Rheumatology, 2021Purpose of review Familial Mediterranean fever (FMF) is the prototypic autoinflammatory disease. Although the gene associated with the disease was identified 24 years ago, we still have to learn about the pathogenesis of its inflammation and the variation in the phenotype. In this review, we discuss some recent findings in FMF,
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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 +20 more
semanticscholar +1 more source
OBJECTIVES Familial Mediterranean fever (FMF) is the most common monogenic autoinflammatory disease despite being a rare disease for many rheumatologists.
Seza Ozen +20 more
semanticscholar +1 more source
Meningitis in familial mediterranean fever
The American Journal of Medicine, 1988Familial Mediterranean fever (FMF) is an inherited autosomal recessive disorder characterized by recurrent, self-limited attacks of fever and serosal inflammation [1-4]. The disease is most commonly encountered in patients of Armenian, Jewish, and Arab origin, but has also been sporadically found in many other ethnic groups [4].
A D, Schwabe, J B, Monroe
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FAMILIAL MEDITERRANEAN FEVER IN AUSTRALIA
Medical Journal of Australia, 1980A case of familial Mediterranean fever is presented, which is, as far as it could be ascertained, the first reported case of this condition in Australia. The difficulties encountered in making this diagnosis are discussed along with diagnostic criteria necessary to substantiate a diagnosis of familial Mediterranean fever.
M D, Smith, R C, Angove
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Jornal de Pediatria, 2019
Objectives To describe a cohort of pediatric patients diagnosed with periodic fever aphthous stomatitis, pharyngitis and adenitis (PFAPA) and familial Mediterranean fever (FMF) and compare them with children diagnosed solely with PFAPA (sPFAPA).
Y. B. Aviel +6 more
semanticscholar +1 more source
Objectives To describe a cohort of pediatric patients diagnosed with periodic fever aphthous stomatitis, pharyngitis and adenitis (PFAPA) and familial Mediterranean fever (FMF) and compare them with children diagnosed solely with PFAPA (sPFAPA).
Y. B. Aviel +6 more
semanticscholar +1 more source
American Journal of Diseases of Children, 1978
A case of familial Mediterranean fever in a young girl presented typical diagnostic dilemmas. Although intermittent proteinuria was noted, a rectal biopsy specimen failed to demonstrate the presence of amyloidosis. Treatment consisted of supportive therapy and colchicine, to which she responded.
E A, Nichols, R F, Reder
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A case of familial Mediterranean fever in a young girl presented typical diagnostic dilemmas. Although intermittent proteinuria was noted, a rectal biopsy specimen failed to demonstrate the presence of amyloidosis. Treatment consisted of supportive therapy and colchicine, to which she responded.
E A, Nichols, R F, Reder
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Familial Mediterranean Fever in Siblings
The Journal of Rheumatology, 2012Objective.Genetic and environmental factors have been implicated in disease severity and development of amyloidosis in familial Mediterranean fever (FMF). We investigated similarities in clinical characteristics, disease severity, and treatment response within siblings with FMF.Methods.The study group consisted of 2 or more siblings who were followed ...
Z Birsin, Özçakar +3 more
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The expanded spectrum of arthritis in children with familial Mediterranean fever
Clinical Rheumatology, 2022P. O. Avar-Aydın +5 more
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