Results 81 to 90 of about 5,699 (211)

Targeted Anti‐Inflammatory Therapy in Cardiovascular Events: Challenges and Opportunities

open access: yesThe Journal of Clinical Hypertension, Volume 27, Issue 11, November 2025.
ABSTRACT Cardiovascular diseases (CVDs) remain the leading cause of morbidity and mortality globally. Emerging evidence suggests that inflammation plays a pivotal role in the pathogenesis of atherosclerosis and subsequent cardiovascular events. Traditional treatments primarily focus on lipid‐lowering and antithrombotic strategies; however, these ...
Li Feng   +3 more
wiley   +1 more source

Neurological Manifestations in Familial Mediterranean Fever: a Genotype-Phenotype Correlation Study

open access: yes
Background and Aims: Familial Mediterranean Fever (FMF) is a periodic auto-inflammatory disease with an autosomal recessive hereditary pattern. The aim of this study is to explain the spectrum of possible neurological manifestations and its genotype ...
مرتضایی, مریم   +4 more
core   +1 more source

Biologics and Small‐Molecule Therapies in Netherton Syndrome: A Comprehensive Review

open access: yesThe 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

DIAGNOSTIC APROACH TO FAMILIAL MEDITERRANEAN FEVER

open access: yesEurasian Journal of Medicine, 2019
Familial Mediterranean fever (FMF) is an autosomal recessively inherited disease, affecting mainly people of Jewish, Arabic, Turkish and Armenian ancestry.
Celalettin Koşan
doaj  

MEFV gene mutation spectrum in familial Mediterranean fever (FMF)

open access: yes, 2011
Familial Mediterranean fever (FMF), an autosomal recessive autoinflammatory disorder, is characterized by recurrent, self-limiting fever and serositis which is frequently seen in Mediterranean populations.
Colak, A.   +9 more
core   +1 more source

Vasculitis and long standing ankylosing spondylitis in a patient with familial Mediterranean fever

open access: yesJournal of Research in Medical Sciences, 2014
Coexistence of familial Mediterranean fever (FMF) and other inflammatory disorders has been frequently reported, but no specific underlying factor has been identified.
Ali Taylan   +3 more
doaj  

Gastric, Colonic, and Rectal Amyloidosis in the Setting of Familial Mediterranean Fever: A Unique Cause of Intractable Diarrhea

open access: yesCase Reports in Gastrointestinal Medicine
Familial Mediterranean fever (FMF) is a hereditary disorder characterized by episodes of fever, polyserositis, or cutaneous inflammation. The FMF attacks last 1–3 days and have no apparent triggers.
Lefika Bathobakae   +6 more
doaj   +1 more source

Interferon-gamma levels in familial Mediterranean fever

open access: yes, 2005
Aims. - To evaluate the levels of endogenous interferon-gamma (IFN-gamma) in patients with familial Mediterranean fever (FMF)
Ihsan Ertenli   +11 more
core   +1 more source

Familial Mediterranean fever in northwest of Iran (Ardabil): the first global report from Iran

open access: yesThe Turkish Journal of Pediatrics, 2008
Familial Mediterranean fever (FMF), which is the prototype of the hereditary periodic fever syndromes, is common in the countries around the Mediterranean Sea.
Farhad Salehzadeh   +10 more
doaj  

Pharmaceutical aspects of familial Mediterranean fever

open access: yes, 2023
Das familiäre Mittelmeerfieber (FMF) ist eine autoinflammatorische Erkrankung, die häufig in Populationen mediterranen Ursprungs auftritt.Obwohl das familiäre Mittelmeerfieber in der Bevölkerung des östlichen Mittelmeerraums im Allgemeinen verbreitet ist,
Demir, Tugba
core   +1 more source

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