Results 61 to 70 of about 5,699 (211)

Nonalcoholic fatty liver disease and familial Mediterranean fever: Are they related? [PDF]

Srpski Arhiv za Celokupno Lekarstvo, 2012
Introduction. Familial Mediterranean fever (FMF) is a periodic febrile disease characterized by acute recurrent episodes of serositis. Liver disease is not considered a part of the spectrum of clinical manifestations of FMF. Objective.
Sarkis Cihat, Caglar Erkan, Ugurlu Serdal, Cetinkaya Emel, Tekin Nilüfer, Arslan Mubeccel, Özdemir Sebati, Tuncer Murat   +7 more
doaj   +1 more source

Oral health status in children with familial Mediterranean fever

, 2021
Background. Familial Mediterranean fever (FMF) is the most common hereditary autoinflammatory disease.
UZAMIŞ TEKÇİÇEK, MERYEM, BİLGİNER, YELDA, Ezgi Deniz Batu, Tülin İleri Keçeli, Pelin Esmeray, Yelda Bilginer, BATU AKAL, EZGİ DENİZ, Esmeray, Pelin, İLERİ KEÇELİ, TÜLİN, Arici, Zehra Serap, ÖZEN, SEZA, KONŞUK ÜNLÜ, HANDE, Zehra Serap Arıcı, Meryem Tekçiçek, Hande Konşuk Ünlü, Seza Özen   +15 more
core   +1 more source

ABCB1 Polymorphisms Influence on Temozolomide Resistance and Overall Survival in Glioblastoma Patients: A Systematic Review of Clinical Evidence

Journal of Cellular and Molecular Medicine, Volume 30, Issue 7, April 2026.
ABSTRACT Glioblastoma (GB), defined as IDH‐wildtype CNS WHO grade 4 tumour according to the 2021 WHO classification of CNS tumours, remains a uniformly lethal malignancy in which the efficacy of temozolomide (TMZ) continues to be constrained by both intrinsic tumur biology and the pharmacological barrier imposed by the blood–brain barrier (BBB).
Fabiola De Luca, Deborah Mannino, Anna Paola Capra, Giuliana Ciappina, Marco Donato, Giuseppe Caruso, Emanuela Esposito, Alessio Ardizzone   +7 more
wiley   +1 more source

Familial Mediterranean Fever and Transverse Myelitis: A Causal Relation?

Neurology and Therapy, 2023
Familial Mediterranean fever (FMF) is a rare autoinflammatory disorder characterized mainly by recurrent self-limited episodes of fever and polyserositis.
Ali Motahharynia, Ghazaal Alavi Tabatabaei, Reza Sarrafi, Saba Naghavi, Iman Adibi   +4 more
doaj   +1 more source

Kidney transplantation in a patient with familial mediterranean fever complicated by secondary amyloidosis (clinical report)

Вестник трансплантологии и искусственных органов, 2023
The paper presents a clinical case of successful kidney transplantation (KTx) in a patient with end-stage chronic kidney disease (ESKD) resulting from familial Mediterranean fever (FMF).
K. G. Tayler, Sh. R. Galeev
doaj   +1 more source

Tuberculosis Presenting as Migratory Arthritis: A Case Report from Iraq

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Extrapulmonary tuberculosis is uncommon, and musculoskeletal involvement presenting as migratory arthritis is particularly rare in immunocompetent individuals, often leading to misdiagnosis and delayed treatment. We report the case of a 66‐year‐old man with diabetes mellitus who presented with recurrent migratory inflammatory arthritis ...
Farah Jaafar Mahdi, Mariam Salem Othman, Ahmed Dheyaa Al‐Obaidi, Mustafa Almusawi, Marafi Jammaa Ahmed, Aya Ahmed Shimal, Elian Khalafalla Awadalla, Marwah Algodi   +7 more
wiley   +1 more source

Attacks of severe dysmenorrhea as the sole manifestation of Familial Mediterranean Fever (FMF) [PDF]

Pediatric Rheumatology, 2008
Familial Mediterranean Fever (FMF) is an autosomal recessive disease (MEFV gene) characterized by recurrent fever and inflammatory serositis. Although majority of patients have random pattern of attacks, some reports described precipitating factors. A literature review indicated that FMF attacks occurring only during menstruation are rarely seen.
VITALE A., LA TORRE F, CARUSO C, FEDE, Carmelo Mario, CALCAGNO, Giuseppina   +4 more
openaire   +3 more sources

Exploring Diagnostic Challenges: A Case Report Commentary on “Solving a Diagnostic Dilemma in a Patient With Periodic Fever—When the Pieces of the Puzzle Finally Fit” [PDF]

Clin Case Rep
ABSTRACT This case highlights the diagnostic challenge of distinguishing periodic fever syndromes with prominent neurological features from interferonopathies. While the absence of specific features on MRI/MRA and SAVI reduces the likelihood of certain subtypes, genetic evaluation involving interferon pathway genes remains important.
Kelesoglu F, Polat A.
europepmc   +2 more sources

Familial Mediterranean Fever

, 2015
Familial Mediterranean Fever (FMF) is an autosomal recessive hereditary disease that affects mainly the people of Jewish, Arabic, Turkish, and Armenian origins.
Yilmaz, Yunus, Ustebay, Sefer, Ustebay, DÖNDÜ ÜLKER   +2 more
core   +1 more source

Familial mediterranean fever and immunoglobulin A nephropathy: A case report and review of the literature

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