Results 51 to 60 of about 5,699 (211)

Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever

Case Reports in Medicine, 2016
Familial Mediterranean fever (FMF) is an autoinflammatory disorder with autosomal recessive inheritance, characterized by recurrent fever and episodes of serositis.
Yunus Ugan, Atalay Doğru, Hüseyin Şencan, Mehmet Şahin, Şevket Ercan Tunç   +4 more
doaj   +1 more source

Polyarteritis nodosa in case of familial Mediterranean fever

The Turkish Journal of Pediatrics, 2018
Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurrent self-limited attacks of fever accompanied by peritonitis, pleuritis, and arthritis.
İbrahim Gökçe, Ülger Altuntaş, Deniz Filinte, Harika Alpay   +3 more
doaj   +1 more source

Public health reforms and the mortality decline in nineteenth‐century Italy

The Economic History Review, Volume 79, Issue 2, Page 527-554, May 2026.
Abstract This study examines the impact of Italy's 1887–8 health reforms on mortality, contributing to the historical debate on the state's role in Europe's health transition. Leveraging event‐study‐style difference‐in‐differences approach, we assess the effectiveness of the Crispi–Pagliani reforms, which strengthened public health governance and ...
Francesco Maria Salvatore Fiore Melacrinis, Mauro Rota   +1 more
wiley   +1 more source

Role of non-invasive methods in detecting liver impairment in familial Mediterranean fever adult patients with persistent hepatic cytolysis

Scientific Reports, 2022
Familial Mediterranean fever (FMF) patients may have hepatic cytolysis, although its origin is not formally elucidated. We aimed to evaluate liver involvement in familial Mediterranean fever (FMF) using non-invasive methods.
Samuel Deshayes, Thibault Fraisse, Soraya Fellahi, Olivier Steichen, Léa Savey, Bruno Turlin, Mona Munteanu, Achille Aouba, Rim Bourguiba, Véronique Hentgen, Jean-Manuel Faintuch, Irina Giurgea, Gilles Grateau, Jean-Philippe Bastard, Sophie Georgin-Lavialle   +14 more
doaj   +1 more source

Adalimumab‐responsive Monogenic Inflammatory Bowel Disease With Pseudopolyposis Characteristic of TGFBR2 Variant in Loeys‐Dietz Syndrome

DEN Open, Volume 6, Issue 1, April 2026.
ABSTRACT Loeys‐Dietz syndrome (LDS) is an autosomal dominant connective tissue disorder caused by pathogenic variants in TGFBR1 or TGFBR2. It is characterized by vascular fragility, skeletal abnormalities, and predisposition to allergic and inflammatory conditions, including monogenic inflammatory bowel disease (IBD).
Tomomitsu Sado, Satoshi Ukai, Shingo Kurasawa, Yosuke Kono, Norio Hasuda, Mai Iwaya, Takaya Nakane, Tomomi Yamaguchi, Tomoki Kosho, Yoshiko Nakayama   +9 more
wiley   +1 more source

Familial Mediterranean Fever (FMF) in Turkey Results of a Nationwide Multicenter Study

, 2005
: Familial Mediterranean fever (FMF) is an autosomal recessive disease that is prevalent among eastern Mediterranean populations, mainly non-Ashkenazi Jews, Armenians, Turks, and Arabs.
Turkish FMF Study Group*
core   +1 more source

Colchicine has Dose‐Dependent Therapeutic Effects in a LPS‐Induced Experimental Endotoxemia Model

Pharmacology Research &Perspectives, Volume 14, Issue 2, April 2026.
ABSTRACT Colchicine is an ancient medication that has long been used for anti‐inflammatory properties. Because of unfavorable and toxic consequences of colchicine, selecting an appropriate dose is critical. The effects of three different doses (0.5, 1 or 5 mg/kg) of colchicine were evaluated.
Meliksah Demir, Ayse Yesim Gocmen, Esin Ozcelebi, Zuleyha Doganyigit, Aslı Okan Oflamaz, Alper Bektas Iskit   +5 more
wiley   +1 more source

Musculoskeletal manifestations occur predominantly in patients with later-onset familial Mediterranean fever: Data from a multicenter, prospective national cohort study in Japan [PDF]

, 2018
BACKGROUND: We showed previously that Japanese individuals with familial Mediterranean fever (FMF) have a more atypical phenotype compared to endemic areas.
Ayuko Takatani (4003193), Akihiro Yachie (739217), Igawa, Takashi, Fujita, Yuya, Midori Ishida, Kiyoshi Migita (290200), Iwamoto, Naoki, Yuya Fujita (5997464), Hideki Nakamura, Takashi Igawa, Ayako Nishino (4003187), Umeda, Masataka, Atsushi Kawakami (398370), Tsuji, Sosuke, Kazunaga Agematsu (398352), Tomoki Origuchi, Shin-ya Kawashiri (4003199), Sumiyoshi, Remi, Hideki Nakamura (1543762), Kawashiri, Shin-ya, Tomoki Origuchi (739149), Ayuko Takatani, Kiyoshi Migita, Yuya Fujita, Junya Masumoto, Takatani, Ayuko, Tomohiro Koga (398369), Ishida, Midori, Ayako Nishino, Agematsu, Kazunaga, Junya Masumoto (277060), Atsushi Kawakami, Naoki Iwamoto, Kunihiro Ichinose (4003172), Toshimasa Shimizu, Shoichi Fukui, Sosuke Tsuji (4003196), Shin-ya Kawashiri, Kawakami, Atsushi, Shimizu, Toshimasa, Remi Sumiyoshi, Masumoto, Junya, Akihiro Yachie, Remi Sumiyoshi (5997467), Koga, Tomohiro, Tamai, Mami, Shoichi Fukui (4003181), Masataka Umeda, Nishino, Ayako, Midori Ishida (5997461), Naoki Iwamoto (4003208), Yushiro Endo, Endo, Yushiro, Mami Tamai (4003175), Tomohiro Koga, Toshimasa Shimizu (4003184), Masataka Umeda (1543771), Yushiro Endo (5997458), Mami Tamai, Migita, Kiyoshi, Sosuke Tsuji, Kazunaga Agematsu, Origuchi, Tomoki, 遠藤, 友志郎, Fukui, Shoichi, Takashi Igawa (5700311), Nakamura, Hideki, Yachie, Akihiro, Ichinose, Kunihiro, Kunihiro Ichinose   +69 more
core   +1 more source

Clinical characteristics of autoimmune glial fibrillary acidic protein astrocytopathy in adults: a retrospective analysis of 9 cases

Internal Medicine Journal, Volume 56, Issue 4, Page 589-597, April 2026.
Abstract Background To identify early diagnostic clues, we analysed cerebrospinal fluid and serum biomarkers in patients with autoimmune glial fibrillary acidic protein astrocytopathy (GFAP‐A) and compared biomarker trends with those in patients with viral meningoencephalitis, tuberculous meningoencephalitis, and anti‐N‐methyl‐D‐aspartate receptor ...
Siruo Guo, Jinyu Huang, Tingting Liu, Wu Yang   +3 more
wiley   +1 more source

MEFV mutations in Northwest of Iran: a cross sectional study [PDF]

Iranian Journal of Basic Medical Sciences, 2015
Objective(s):Familial Mediterranean Fever (FMF) is an autosomal recessive disorder characterized by recurrent episodes of fever accompanied by peritonitis, pleurisy, and arthritis.
Morteza Jabbarpour Bonyadi, Sousan Mir Najd Gerami, Mohammad Hossein Somi, Saeed Dastgiri   +3 more
doaj