Results 51 to 60 of about 12,115 (183)

De Stupro: First Insights on Rape and Its Prosecution in Maltese Courts (1701–10)

Journal for Eighteenth-Century Studies, EarlyView.
Abstract This article constitutes a first in‐depth investigation of rape and the prosecution of this crime in early eighteenth‐century Malta. The research, which is based on sixteen rape accusations claimed at the secular courts in Malta between 1701 and 1710, has analysed cases categorized as ‘simple rape’, ‘violent rape’ and rape committed under the ...
Vanessa Buhagiar
wiley   +1 more source

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

Orbital muscle involvement in a child with familial Mediterranean fever

, 2021
Familial Mediterranean fever is an autosomal recessively inherited autoinflammatory disorder characterized by recurrent attacks of fever, serositis and synovitis. Various atypical presentations have been reported in the literature.
Keskindemirci, Gonca, Cakan, Mustafa, Aktay Ayaz, Nuray, Bayramoglu, Sadik Etka, Genc, Hamide Sevinc, Er, Ali   +5 more
core   +1 more source

An Atypical Skin Presentation of Adult‐Onset Still's Disease With Histological Description: A Case Report

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Adult‐onset Still's disease (AOSD) is an auto inflammatory disorder with a variable clinical presentation, and without a pathognomonic diagnostic test, characterized by high spiking fever, arthralgia/arthritis, a suggestive skin rash, elevated white blood cell count 10 G/L (> 80% neutrophils), elevated ferritin, with glycosylated ferritin < 20%
M. Nordmann, T. Mazza, S. Menzinger, G. Kaya, S. Bogiatzi, S. Vandenberghe‐Dürr, M. Blanchard, J. Stirnemann   +7 more
wiley   +1 more source

Characterizing MEFV gene variants in Jordanian patients with Familial Mediterranean Fever

Human Genomics
Background Familial Mediterranean Fever (FMF) is inherited as an autosomal recessive autoinflammatory disorder caused by mutations in the Mediterranean fever (MEFV) gene and predominantly affects populations from the Mediterranean region.
Wissam A. Alwazani, Nisreen A. Fuqaha, Zekrayat Medras, Yaqeen A. Rjoub, Kholoud Altaany   +4 more
doaj   +1 more source

Familial Mediterranean Fever: Current Approaches to Diagnosis and Treatment

Вопросы современной педиатрии, 2018
Familial Mediterranean fever is a typical monogenic disease with an autosomal recessive inheritance pattern; caused by mutations in the MEFV gene, which encodes the pyrin protein.
Mikhail M. Kostik, Olga V. Zhogova, Natalia V. Lagunova, Sergey V. Ivanovskiy, Oksana L. Kolobova, Larisa N. Melnikova   +5 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

Australian clinical practice guideline: diagnosis and treatment of idiopathic multicentric Castleman disease

Internal Medicine Journal, EarlyView.
Abstract Idiopathic multicentric Castleman disease (iMCD) is a rare condition. The pathogenesis is incompletely understood; however, interleukin‐6 (IL‐6) is a major mediator. The clinical presentation is heterogeneous, from mild constitutional symptoms to severe multi‐organ failure.
Dipti Talaulikar, Jun Yen Ng, Adam Bryant, Annmarie Bosco, Hugh C. Caterson, Pratyush Giri, Pravin Hissaria, Simon J. Harrison, Stephen Lade, Connull Leslie, Jacinta Perram, H. Miles Prince, Dejan Radeski, Maureen Rischmueller, Craig Wallington‐Gates, Nicholas Weber, Alberta Hoi   +16 more
wiley   +1 more source

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  

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