Results 31 to 40 of about 739,257 (226)

MEDITERRANEAN OR MALTA FEVER, [PDF]

The Lancet, 1899
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Birt, C., Lamb, G.
openaire   +1 more source

THE PREVALENCE OF CELIAC DISEASE AMONG PATIENTS WITH FAMILIAL MEDITERRANEAN FEVER

Arquivos de Gastroenterologia, 2015
Background Familial Mediterranean Fever and celiac disease are both related to auto-inflammation and/or auto-immunity and they share some common clinical features such as abdominal pain, diarrhea, bloating and flatulence. Objectives We aimed to determine
Sedat IŞIKAY, Nurgül IŞIKAY, Halil KOCAMAZ   +2 more
doaj   +1 more source

Awareness and knowledge of familial Mediterranean fever among medical scope students in Syrian universities: A cross-sectional study

SAGE Open Medicine, 2023
Introduction: Familial Mediterranean fever is an autoinflammatory autosomal recessive disorder common among individuals of Mediterranean descent. It is characterized by recurrent episodes of fever accompanied by peritonitis, pleurisy, pericarditis, and ...
Jamal Ataya, Jameel Soqia, Massa Alfawal, Nour Kara Tahhan, Nour Albani, Yahya Hani   +5 more
doaj   +1 more source

Increased levels of circulating Annexin A5 in Familial Mediterranean fever

Journal of Inflammation, 2010
Background Familial Mediterranean fever is a genetic autoinflammatory disease most commonly affecting the ethnic groups originating from around the Mediterranean Sea.
Hovhannisyan Lilit P, Mkrtchyan Gohar M, Boyajyan Anna S, Hovsepyan Tigran J   +3 more
doaj   +1 more source

Familial Mediterranean Fever without Fever

Internal Medicine, 2020
Familial Mediterranean fever (FMF) is an autosomal recessive hereditary disease commonly observed around the Mediterranean basin presenting as recurrent febrile episodes. We herein describe a Japanese case of genetically-confirmed FMF, in which fever was lacking during attacks.
Hotta, Yuma, Kawasaki, Tatsuya, Kotani, Tomoya, Okada, Hiroshi, Ikeda, Kanami, Yamane, Satoki, Yamada, Nobuhisa, Sekoguchi, Satoru, Isozaki, Yutaka, Nagao, Yasuyuki, Murotani, Masahiro, Oyamada, Hirokazu   +11 more
openaire   +3 more sources

Evaluation of Cardiac Arrhythmia Susceptibility in Pediatric Familial Mediterranean Fever Patients

Journal of Contemporary Medicine, 2023
Aim: Familial Mediterranean fever is an autoinflammatory disease characterized by attacks of inflammation. Despite treatment, there is evidence of subclinical persistence of inflammation with normal laboratory values.
Vildan Güngörer, Ahmet Sert, Şükrü  Arslan   +2 more
doaj   +1 more source

Comparison of optical coherence tomography angiography results of adult patients with Familial Mediterranean fever and healthy individuals

Therapeutic Advances in Ophthalmology, 2019
Purpose: The aim of this study is to assess the macular ultrastructure measuring by optical coherence tomography angiography in adult patients with Familial Mediterranean fever.
Emine Esra Karaca, Dilay Ozek, Ahmet Omma, Ozlem Evren Kemer   +3 more
doaj   +1 more source

Living kidney transplantation between brothers with unrecognized renal amyloidosis as the first manifestation of familial Mediterranean fever: a case report

BMC Medical Genetics, 2017
Background Familial Mediterranean fever is an autosomal recessive disease characterized by recurrent episodes of fever and polyserositis and by the onset of reactive amyloid-associated amyloidosis. Amyloidosis due to familial Mediterranean fever can lead
Ramón Peces, Sara Afonso, Carlos Peces, Julián Nevado, Rafael Selgas   +4 more
doaj   +1 more source

Early Post-transplant Recurrence of Amyloidosis in a Patient with Familial Mediterranean Fever

Turkish Journal of Nephrology, 2021
Familial Mediterranean fever is the most common hereditary auto-inflammatory disease characterized by a recurrent attack of fever and serositis. Untreated patients frequently develop AA type of amyloidosis which results in end-stage kidney disease (ESKD).
Deniz Aral Özbek, Neriman Sıla Koç, Arzu Sağlam, Tolga Yildirim, Şeref Rahmi Yilmaz, Yunus Erdem   +5 more
doaj   +1 more source

A novel single variant in the MEFV gene causing Mediterranean fever and Behçet’s disease: a case report

Journal of Medical Case Reports, 2018
Background Familial Mediterranean fever is an autoinflammatory disease of unknown etiology, characterized clinically by recurrent attacks of sudden-onset fever with arthralgia and/or thoracoabdominal pain and pathogenetically by autosomal recessive ...
Maria Zerkaoui, Fatima Zahra Laarabi, Yousra Ajhoun, Bouchra Chkirate, Abdelaziz Sefiani   +4 more
doaj   +1 more source