Results 31 to 40 of about 848,404 (232)

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.
Şükrü  Arslan, Vildan Güngörer, Ahmet Sert   +2 more
doaj   +1 more source

Autoinflammatory disease: clinical perspectives and therapeutic strategies

Inflammation and Regeneration, 2022
The molecular platforms of the innate immune system are essential to recognize pathologic external factors that are crucial to differentiate these danger signals from host motifs.
Atsushi Kawakami, Endo Yushiro, Koga Tomohiro, Yoshiura Koh-ichiro, Migita Kiyoshi   +4 more
doaj   +1 more source

IgA nephropathy-associated familial Mediterranean fever [PDF]

Journal of Nephropathology
Familial Mediterranean fever is an autosomal recessive autoinflammatory disorder characterized by recurrent episodes of fever, inflammation, and serositis. Individuals with Familial Mediterranean fever (FMF) are at an increased risk of developing various
Saeed Hoseininia, Sousan Mohammadi Kebar
doaj   +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

Dual Biologic Therapy in Patients with Familial Mediterranean Fever and Spondyloarthritis: Case-Based Review

, 2023
Patients with familial Mediterranean fever and spondylitis often fail to respond to conventional and biologic therapies. Achieving remission in these patients usually requires conventional and biologic treatment combinations.
İbrahim Vasi, Riza Can Kardas, Abdurrahman Tufan, Rıza Can Kardaş, Tufan, Abdurrahman, Derya Yıldırım, Hamit Küçük, Kardaş, Rıza Can, Mehmet Akif Öztürk, Özkızıltaş, Burcugul, null null, Burcugul Ozkiziltas, ÖZKIZILTAŞ, BURCUGÜL, Burcugul Özkızıltaş, Yıldırım, Derya, Derya Yildirim, KARDAŞ, RIZA CAN, Vasi, İbrahim, Küçük, Hamit, Öztürk, Mehmet Akif   +19 more
core   +1 more source

The Kidney in Familial Mediterranean Fever [PDF]

The Journal of Rheumatology, 2013
Familial Mediterranean fever (FMF) is a hereditary periodic fever disease that presents with recurrent attacks of peritonitis, pleuritis, arthritis, or erysipelas-like erythema1. The attacks last up to 3 days, with varying degrees of frequency. One of the most devastating complications of the disease is amyloidosis, which primarily affects the kidneys ...
Hagit, Peleg, Eldad, Ben-Chetrit
openaire   +2 more sources

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

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

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

Atypical Familial Mediterranean Fever Complicated with Gastrointestinal Amyloidosis Diagnosed due to Paroxysmal Arthralgia and Intractable Diarrhea, Successfully Treated with Tocilizumab [PDF]

, 2019
A 53-year-old man with recurrent episodes of large joint pain and a low-grade fever at irregular intervals for 16 years developed right knee and ankle arthralgia, watery diarrhea, and abdominal pain.
Okamoto, Momoko, Kawashiri, Shin-ya, Kuroda, Kishio, Irie, Junji, Igawa, Takashi, Eguchi, Mizuna, Kawakami, Atsushi, Shimizu, Toshimasa, Aikawa, Erika, Origuchi, Tomoki, Takatani, Ayuko, Iwamoto, Naoki, Koga, Tomohiro, Tamai, Mami, Nakamura, Hideki, Hori, Tomoko, Umeda, Masataka, Tsuji, Sosuke, Endo, Yushiro, Sumiyoshi, Remi, Ichinose, Kunihiro   +20 more
core   +1 more source