Results 71 to 80 of about 739,257 (226)

Scrutinising Frontex: The European Parliament and Accountability through Discharge

open access: yesJCMS: Journal of Common Market Studies, EarlyView.
Abstract This article examines how the European Parliament (EP) has leveraged the budgetary discharge procedure to enhance the political accountability of the EU's Border and Coast Guard Agency, Frontex. Whilst the procedure is formally limited to budget implementation, the EP has used it as an accountability tool that goes far beyond financial ...
Magnus G. Schoeller, Peter Slominski
wiley   +1 more source

Familial Mediterranean Fever

open access: yes, 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   +2 more
core   +1 more source

Interacting climatic, environmental, biologic and socio‐economic drivers of the global dengue expansion

open access: yesJournal of Internal Medicine, EarlyView.
Abstract Dengue is the most rapidly expanding mosquito‐borne viral disease worldwide. The worst year on record was 2024, with over 100 countries reporting 14.4 million cases and over 11,000 deaths. Since then, and up to August 2026, another 7.4 million cases and over 5000 deaths have been reported.
Jan C. Semenza
wiley   +1 more source

Periodic Fever Compatible with Familial Mediterranean Fever.

open access: yesInternal Medicine, 1992
A 55-year-old male presented with a recurrent fever of over 38 degrees C, occurring at irregular intervals 1-6 times a month with chest, back or abdominal pain. After admission to our hospital, we found the following characteristics: 1) the febrile attacks were accompanied by obvious inflammatory findings and pleuritis or peritonitis; 2) the patient's ...
TAKAHASHI, Mayumi   +8 more
openaire   +3 more sources

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)
Ertenli, I   +5 more
core   +1 more source

Catheter‐Associated Urinary Tract Infections in Children: An Evidence‐Informed Narrative Review of Diagnosis, Management and Prevention

open access: yesJournal of Paediatrics and Child Health, EarlyView.
ABSTRACT Catheter‐associated urinary tract infections (CAUTI) are a common healthcare‐associated infection in children and a major contributor to increased morbidity, prolonged hospital stays and higher healthcare costs. This narrative review uses an evidence‐informed approach highlighting recent paediatric literature (2000–2025) to provide an overview
Simon P. Paget   +4 more
wiley   +1 more source

Familial Mediterranean fever in northwest of Iran (Ardabil): The first global report from Iran [PDF]

open access: yes
Familial Mediterranean fever (FMF), which is the prototype of the hereditary periodic fever syndromes, is common in the countries around the Mediterranean Sea. Considering its geographical position in the northwest of Iran, with its population of Turkish
فیضی, ایرج   +10 more
core  

Geographical distribution of Hyalomma marginatum Koch, 1844 in northwestern Spain from 2019 to 2024: A one health approach

open access: yesMedical and Veterinary Entomology, EarlyView.
This study confirms the presence of the tick Hyalomma marginatum Koch, 1844, a known vector of the Crimean‐Congo hemorrhagic fever virus at Galicia. Most ticks were encountered on humans and livestock, with numbers rising between 2019 and 2024, especially during spring and in warm‐summer Mediterranean southwest areas of the studied region.
Inês Abreu Ramos   +10 more
wiley   +1 more source

A Case Of Familial Mediterranean Fever Presenting With Protracted Febrile Myalgia Syndrome

open access: yes, 2008
Familial Mediterranean fever is the most common in the hereditary periodic fever syndromes. The frequency of vasculitis syndromes are high in familial Mediterranean fever population.
Cüneyt Karagöl   +3 more
core  

Clinicogenetic Characterization of H Syndrome in a South African Child

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT H syndrome is a rare autosomal recessive genodermatosis caused by loss‐of‐function SLC29A3 variants, combining hyperpigmented indurated plaques and hypertrichosis with life‐threatening autoinflammation. We report a 5‐year‐old South African girl of first‐cousin parents who presented with hyperinflammation mimicking macrophage activation ...
Tshimogo Tswelopele Sathekge   +1 more
wiley   +1 more source

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