Results 51 to 60 of about 7,121 (223)
Radiology Case Reports, 2021 Familial Mediterranean Fever (FMF) is an autosomal recessive disorder that is characterised by recurrent attacks of fever and painful polyserositis mainly affecting the peritoneum, synovium and pleura that usually begins in childhood.
A. Abdalla Ibrahim, MD +2 more
doaj +1 more source
Attacks of pericarditis as a manifestation of familial Mediterranean fever (FMF) [PDF]
QJM, 1997 Familial Mediterranean fever (FMF) is characterized by recurrent attacks of febrile serositis. While arthritis, pleuritis and peritonitis are common in FMF, no association of pericarditis with FMF has been described in detail. We retrospectively studied about 4000 FMF patients, using a computer chart review.
S, Kees +5 more
openaire +2 more sources
Biologics and Small‐Molecule Therapies in Netherton Syndrome: A Comprehensive Review
The Journal of Dermatology, Volume 52, Issue 10, Page 1483-1493, October 2025.ABSTRACT Netherton syndrome (NS) is a rare congenital ichthyosis caused by loss‐of‐function mutations in the SPINK5 gene, leading to defective expression of the serine protease inhibitor LEKTI. Dysregulated epidermal protease activity results in impaired skin barrier function and chronic inflammation, accompanied by complex immune profiles. NS patients
Shin Morizane +6 more
wiley +1 more source
MEFV mutations in Northwest of Iran: a cross sectional study [PDF]
Iranian Journal of Basic Medical Sciences, 2015 Objective(s):Familial Mediterranean Fever (FMF) is an autosomal recessive disorder characterized by recurrent episodes of fever accompanied by peritonitis, pleurisy, and arthritis.
Morteza Jabbarpour Bonyadi +3 more
doaj
Saudi Journal of Kidney Diseases and Transplantation, 2020 Familial Mediterranean fever (FMF) is an autosomal recessive disease charac-terized by recurrent fever episodes and polyserositis. The most important complication is amyloidosis. Nonamyloidotic nephropathy in FMF is poorly documented. Besides amyloidosis,
Fatih Yılmaz, Meryem Keleş
doaj +1 more source
The burgeoning field of innate immune-mediated disease and autoinflammation. [PDF]
, 2016 Immune-mediated autoinflammatory diseases are occupying an increasingly prominent position among the pantheon of debilitating conditions that afflict mankind.
McDermott, MF +3 more
core +1 more source
Journal of Clinical Nursing, Volume 34, Issue 9, Page 3650-3659, September 2025.ABSTRACT Background The infection prevention behaviours of kidney transplant recipients have been investigated, but the factors affecting these have not. Therefore, the present study aimed to examine the infection prevention behaviours of kidney transplant recipients and the factors related to these.
Yaprak Sarıgöl Ordin +1 more
wiley +1 more source
GSDMD is critical for autoinflammatory pathology in a mouse model of Familial Mediterranean Fever [PDF]
, 2018 Pyroptosis is an inflammasome-induced lytic cell death mode, the physiological role of which in chronic inflammatory diseases is unknown. Familial Mediterranean Fever (FMF) is the most common monogenic autoinflammatory disease worldwide, affecting an ...
Chi, Hongbo +11 more
core +1 more source
British Journal of Haematology, Volume 207, Issue 2, Page 387-394, August 2025.Individuals who may develop multiple myeloma within 5 years. Stage I (left) identifies patient and control groups and variables that differ between them. Stage II (middle) develops a complex SGBOOST model to predict future MM patients. Stage III (right) develops a simplified model.
Moshe Mittelman +8 more
wiley +1 more source
Clinical Medicine Insights: Case Reports, 2018 Familial Mediterranean fever (FMF) is characterized by recurrent episodes of fever accompanied by serosal, synovial, or cutaneous inflammation. The central nervous system (CNS) is rarely involved in FMF. The CNS involvement includes demyelinating lesions,
Miramir Aghdashi +3 more
doaj +1 more source