Results 81 to 90 of about 848,404 (232)

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

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, خلفی, جعفر, صالح زاده, فرهاد, عظیمی, هرمز, ذولفقاری, علی اصغر, براک, منوچهر, جستان, مارینا, حبیب زاده, شهرام, امامی, دینا, یزدانبد, عباس, بشردوست, بهمن   +10 more
core  

Comparison of Different Pharmaceutical Preparations of Colchicine in Children with Familial Mediterranean Fever: Is Colchicine Opocalcium a Good Alternative?

, 2021
Background: Colchicine is an anti-inflammatory agent used for preventing familial Mediterranean fever (FMF) attacks and amyloidosis.
Selçuk Yüksel, Unsal, Erbil, Serkan Türkuçar, Makay, BALAHAN, Acari, Ceyhun, Balahan Makay, Yukser, Selcuk, Yuksel, Selcuk, Ceyhun Acari, Gülçin Otar Yener, Erbil Ünsal, Turkucar, Serkan, Yener, Gulcin Otar, Hatice Adıgüzel Dundar, Dundar, Hatice Adiguzel   +14 more
core   +1 more source

Renal and suprarenal insufficiency secondary to familial Mediterranean fever associated with amyloidosis: a case report

Journal of Medical Case Reports, 2011
Introduction Familial Mediterranean fever is an autosomal recessive disease that predominantly affects people of the Mediterranean coast. One of the most frequent complications of the disease is amyloidosis.
Sari Nagehan, Erdenen Fusun, Toros Ahmet, Gokcay Serkan   +3 more
doaj   +1 more source

The Impact of Hidradenitis Suppurativa on Sexual Function: A Multicentered Cross‐Sectional Study

International Journal of Dermatology, EarlyView.
Summary of a multicenter study of 522 patients with hidradenitis suppurativa (HS) evaluating quality of life, disease severity, and sexual function. HS was associated with impaired sexual function in both women and men, with pain identified as a central driver.
Defne Özkoca, Hediye Eker, Dilay Yerlioğlu Ak, Beril Kara Esen, Ali Emre Buğday, Tuğba Tehçi, Neslihan Demirel Öğüt, Ayris Öztürk, Algün Polat Ekinci, Özlem Su Küçük, Erkan Alpsoy, Aslı Tatlıparmak, Esra Adışen, Ecem Etli, Fatma Etgü, Gülhan Aksoy Saraç, Ersoy Acer, Esra Ağaoğlu, Münevver Güven, Zeynep Karaca Ural, Rabia Öztaş Kara, Ahmet Uğur Atılan, Gözde Ulutaş Demirbaş, Gülhan Gürel, Seçil Vural   +24 more
wiley   +1 more source

Coexistence of Familial Mediterranean Fever, Behçet’s Disease and Sacroiliitis

The Turkish Journal of Gastroenterology, 2015
Familial Mediterranean fever is a genetic disorder restricted to certain ethnic groups and marked by acute attacks of serositis and the insidious development of amyloidosis.
İsmihan SUNAR, Zühre SARI SÜRMELİ, Ali Erhan ÖZDEMİREL, Ayşe Peyman YALÇIN, Şebnem ATAMAN   +4 more
doaj  

Two cases of periodic fever syndrome with coexistent mevalonate kinase and Mediterranean fever gene mutations

The Turkish Journal of Pediatrics, 2017
The periodic fever syndromes are autoinflammatory diseases that present with recurrent fever, serositis and rash. Familial Mediterranean fever is the most common periodic fever syndrome and characterized by recurrent attacks of fever, arthritis ...
Mustafa Çakan, Nuray Aktay-Ayaz, Gonca Keskindemirci, Şerife Gül Karadağ   +3 more
doaj   +1 more source

AA amyloidosis in the four historical monogenic autoinflammatory diseases: Clinical burden and insights from a retrospective referral‐centre study

Journal of Internal Medicine, EarlyView.
Abstract Background AA amyloidosis (AAA) remains a life‐threatening yet largely preventable complication of monogenic autoinflammatory diseases (AIDs). Methods We retrospectively described patients with AAA secondary to one of the four historical monogenic AIDs (familial Mediterranean fever [FMF], cryopyrin‐associated periodic syndrome [CAPS ...
Majdouline El Moussaoui, Léa Savey, Hassina Sofia Aloui‐Belhocine, Jean‐Jacques Boffa, Marion Delplanque, Catherine Grandpeix‐Guyodo, Irina Giurgea, Laurence Cuisset, Guilaine Boursier, Gilles Grateau, David Buob, Sophie Georgin‐Lavialle   +11 more
wiley   +1 more source

DAPSONE AS AN ALTERNATIVE THERAPY IN CHILDREN WITH FAMILIAL MEDITERRANEAN FEVER [PDF]

Objective: Familial Mediterranan Fever is an hereditary autoinflammatory disease that presents with recurrent febrile attacks and poly serositis. Colchicine is the only known treatment in this diease.
صالح زاده, فرهاد, جهانگیری, سپیده, محمدی کلاسرلو, ایلنار   +2 more
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Catheter‐Associated Urinary Tract Infections in Children: An Evidence‐Informed Narrative Review of Diagnosis, Management and Prevention

Journal 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, Robert McCusker, Suzanne Simpson, Melissa Short, Angela Berkhout   +4 more
wiley   +1 more source

Febrile myalgia syndrome in familial Mediterranean fever

, 2006
Familial Mediterranean fever is characterized by recurrent polyserositis episodes associated with fever. However, the clinical spectrum of this disease has been expanded recently and myalgia is now a frequently recognized component.
SOYLU, ALPER, Saylam, GS, Kavukcu, SALİH, Kasap, B, Turkmen, M   +4 more
core   +1 more source