Results 31 to 40 of about 35,452 (278)

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

Familial Mediterranean fever, from pathogenesis to treatment: a contemporary review

Turkish Journal of Medical Sciences, 2020
Familial Mediterranean fever (FMF) (OMIM #249100) is the most common hereditary autoinflammatory disease in the world. FMF is caused by gain of function mutations of MEFV gene which encodes an immune regulatory protein, pyrin. Over the last few years, we
A. Tufan, H. Lachmann
semanticscholar   +1 more source

Anesthesia experience along with familial Mediterranean fever and celiac disease [PDF]

, 2014
(Anesthetic management in patient with Familial Mediterranean Fever and Celiac Disease) Familial Mediterranean Fever is an autosomal recessive transmitted disease which often seen at Mediterranean origin society and it goes by deterioration at ...
Gülçin Hacıbeyoğlu, Hale Borazan, Mehmet Sargın, Şeref Otelcioğlu   +3 more
core   +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 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

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

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

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

Could pentraxin-3 be a new marker for subclinical inflammation in familial Mediterranean fever? [PDF]

, 2015
Not ...
Evrengül, Harun, Karadağlı, Eda, Yüksel, Selçuk, Şenol, H.   +3 more
core   +1 more source

Ancient familial Mediterranean fever mutations in human pyrin and resistance to Yersinia pestis

Nature Immunology, 2020
Familial Mediterranean fever (FMF) is an autoinflammatory disease caused by homozygous or compound heterozygous gain-of-function mutations in MEFV, which encodes pyrin, an inflammasome protein. Heterozygous carrier frequencies for multiple MEFV mutations
Y. Park, E. Remmers, Wonyong Lee, A. Ombrello, Lawton K. Chung, Shilei Zhao, D. Stone, Maya I. Ivanov, N. Loeven, K. Barron, P. Hoffmann, M. Nehrebecky, Yeliz Z. Akkaya-Ulum, E. Sağ, B. Balcı-Peynircioğlu, I. Aksentijevich, A. Gül, C. Rotimi, Hua Chen, J. Bliska, S. Ozen, D. Kastner, D. Shriner, J. Chae   +23 more
semanticscholar   +1 more source