Results 141 to 150 of about 11,340 (243)

PECU: A multicenter study on pediatric patients with cold‐induced urticaria

Pediatric Allergy and Immunology, Volume 37, Issue 6, June 2026.
Abstract Background Cold‐induced urticaria (ColdU) is a rare chronic inducible urticaria that can cause systemic reactions, including cold‐induced anaphylaxis (ColdA), but pediatric data are limited. The aim of this study was to evaluate the clinical characteristics, comorbidities, management approaches, risk of anaphylaxis, and long‐term course of ...
Betul Gemici Karaaslan, Ozgen Soyoz, Figen Celebi Celik, Humeyra Akbas, Yakup Canitez, H. Ilbilge Ertoy Karagol, Beril Canan Aksoydan, Yagmur Hazal Sadirvan Oguzkaya, Gizem Uslu, Semiha Bahceci Erdem, Ummugulsum Dikici, Hilal Gungor, Handan Duman Senol, Hulya Anil, Adem Yasar, Lida Bulbul, Nursen Cigerci Gunaydin, Ozge Turkyilmaz Ucar, Mehmet Akif Kaya, Sanem Eren Akarcan, Tugba Arikoglu, Ozge Kangalli Boyacioglu, Hatice Eke Gungor, Merve Ocalan, Mahmut Dogru, Mahir Serbes, Nagihan Iskender, Mehmet Kilic, Mutlu Yuksek, Ozlem Yilmaz, Tuba Tuncel, Sefika Ilknur Kokcu Karadag, Zeynep Meric, Tuba Karakurt, Sezin Aydemir, Ugurcan Sayili, Fadil Ozturk, Ozlem Sancakli, Aysen Bingol, Mehmet Halil Celiksoy, Mustafa Atilla Nursoy, Aylin Kont Ozhan, Suna Asilsoy, Ozge Yilmaz, Dilek Ozcan, Isil Eser Simsek, Koray Harmanci, Esen Demir, Deniz Ozceker, Oner Ozdemir, Sukru Cekıc, Mustafa Arga, Ozlem Cavkaytar, Nazli Ercan, Arzu Bakirtas, Zeynep Ulker Altinel, Demet Can, Haluk Cokugras, Esra Yucel, Ayca Kiykim   +59 more
wiley   +1 more source

Is familial Mediterranean fever (FMF) common in patients with negative appendectomy?

, 2013
Familial Mediterranean fever (FMF) is an autosomal-recessive disease characterized by recurrent attacks of fever with serositis. Differential diagnosis of a FMF abdominal attack with acute abdomen is difficult. Acute appendicitis is the most common cause
Karabicak, Ilhan, Ertenli, Ihsan, Tirpanci, Berna, Erol, Mehmet Fatih, Onat, Ahmet Mesut, Ozer, Saadet, Pehlivan, Yavuz, Kisacik, Bunyamin   +7 more
core   +1 more source

Severity scoring system for paediatric FMF [PDF]

Nature Reviews Rheumatology, 2012
Kalkan, Gokhan, Demirkaya, Erkan, Ozen, Seza   +2 more
openaire   +4 more sources

A retrospective comparison of the clinical and demographic characteristics of FMF-associated and non-FMF amyloidosis

Ailevi Akdeniz Ateşi (FMF), ataklar halinde ortaya çıkan ve tekrarlayan ateş, serozit ve sinovit atakları ile karakterize genetik bir hastalıktır. FMF hastalarında hastalığın progresyonunda belirleyici etken sekonder amiloidoz gelişmesidir.
Özkan, Halil İbrahim
core  

Sacroiliitis in familial Mediterranean fever: an unusual presentation in childhood

The Turkish Journal of Pediatrics, 1999
Familial Mediterranean fever (FMF) is an autosomal recessively transmitted disease characterized by attacks of fever and serositis. The course of arthritis, which is a common manifestation of FMF, is generally benign.
N Beşbaş, S Ozdemir, I Saatçi, A Bakkaloğlu, S Ozen, U Saatçi   +5 more
doaj  

Cardiac functions and pericardial thickness changes in familial Mediterranean fever patients

Egyptian Rheumatology and Rehabilitation
Background The goal of the study is to ascertain how the pericardium and heart functions alter in patients with familial Mediterranean fever (FMF) both during the acute phase and the period of subclinical inflammation.
Yasemin Demir Yiğit, Özlem Karakuş Karatoprak, Elif Güzelsoy Ay, Muhammed Karabulut, Erdal Yılmaz, Metin Kaya Gürgöze   +5 more
doaj   +1 more source

Enigmatic link between familial mediterranean fever and dietary components: a novel approach to personalized nutrition

BMC Nutrition
Background Despite its prevalence, Familial Mediterranean Fever (FMF) remains poorly understood, with limited therapeutic options available to manage its debilitating symptoms.
Ninar AlJerf, Abdullah H. Maad, Loai Aljerf, Muaaz Alajlani   +3 more
doaj   +1 more source

Familial Mediterranean fever (FMF) in Iran

, 2016
Background & objectives: FMF is an auto-inflammatory and hereditary periodic disorder. The symptoms can occur in more than 80% during the first decade of life. With regard to high prevalence of FMF in northwest of Iran, this study was conducted 
Morteza Eslami, Farhad Salehzadeh
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Other autoinflammatory disease genes in an FMF-prevalent population: a homozygous MVK mutation and a heterozygous TNFRSF1A mutation in two different Turkish families with clinical FMF

, 2017
Objective. No MEFV mutations are detected in approximately 10% of the patients with clinical FMF in populations where the disease is highly prevalent. Causative mutations were searched in other genes in two such families with "MEFV negative clinical FMF"
Ozdogan, H., Karacan, I., Tolun, A., Turanli, E. Tahir, Ugurlu, S.   +4 more
core  

Do MEFV mutations influence arterial stiffness in FMF patients?

, 2017
Background: Pulse wave velocity (PWV) is the most used technique to evaluate the arterial elasticity, which is an early indicator of atherosclerosis.
Acay, Akif, Ahsen, Ahmet, Solak, Mustafa, Ulu, Memnune Sena, Acartürk, Gürsel, Yuksel, Şeref   +5 more
core