Results 161 to 170 of about 5,699 (211)

Polyarteritis nodosa in patients with Familial Mediterranean Fever (FMF): A concomitant disease or a feature of FMF?

Seminars in Arthritis and Rheumatism, 2001
Familial Mediterranean Fever (FMF) is caused by mutations in the gene encoding pyrin and is characterized by self-limited, recurrent attacks of fever and serositis. Vasculitis has been increasingly reported in FMF. A study evaluating the prognosis in FMF and polyarteritis nodosa (PAN) patients has not been reported previously.To determine the special ...
Eldad Ben-Chetrit, Hanan Gur, K Tinaztepe   +2 more
exaly   +4 more sources

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Dominant inheritance in two families with familial Mediterranean fever (FMF)

American Journal of Medical Genetics Part A, 1995
AbstractFamilial Mediterranean fever (FMF) is an autosomal‐recessive disease which affects almost exclusively people of Mediterranean and Middle Eastern origin. We examined the possibility of a dominant inheritance of FMF among our 3,000 patients in Israel.Two hundred forty FMF patients were members of 77 families in which the disease affected more ...
D Zemer, Mordechai Pras
exaly   +3 more sources

MEFV Mutations in Cases with Familial Mediterranean Fever (FMF) [PDF]

, 2015
Ailesel Akdeniz ateşi (FMF), MEFV genindeki mutasyonların neden olduğu otozomal resesif bir hastalıktır. Bu gen, kromozom 16p13.3'da haritalanmıştır ve özellikle granülositlerde bulunan bir proteini (pirin) kodlamaktadır. Bu çalışmada FMF ön tanısı ile refere edilen 197 olguda MEFV geninde sıklıkla rastlandığı bildirilen E148Q, P369S, F479L, M680I
Yeşilada, Elif, Savacı, Serap, Yüksel, Şengül, Gülbay, Gonca, Otlu, Gonca, Kaygusuzoğlu, Ebru   +5 more
openaire   +3 more sources

Assessment of pyrin gene mutations in Turks with familial Mediterranean fever (FMF)

Human Mutation, 1998
Familial Mediterranean fever (FMF) is an autosomal recessive disease clinically characterized by recurrent short self-limited attacks of fever accompanied by peritonitis, pleurisy, and arthritis and can lead to amyloidosis and renal failure in the longer term. It is prevalent mainly in non-Ashkenazi Jews, Armenians, Turks, and Arabs. Due to the lack of
Xiaoguang Chen, Nathan Fischel-Ghodsian, Melanie A Hamon   +2 more
exaly   +3 more sources

Histopathological characteristics of synovitis in Familial Mediterranean Fever (FMF)

Joint Bone Spine, 2022
N. A.
Venerito V., Portincasa P., Stella A., Cazzato G., Cimmino A., Iannone F., Lopalco G.   +6 more
openaire   +3 more sources

Thoracic and lung involvement in familial Mediterranean fever (FMF)

Clinics in Chest Medicine, 2002
Lung involvement in FMF is limited mainly to transient pleuritis during acute attacks. Amyloidosis of the lung is rare and is associated with symptomatic involvement of other organs while remaining subclinical in itself. Vasculitis of the lung in FMF is possible because of the strong association between FMF and a variety of vasculitides.
Merav, Lidar, Mordechai, Pras, Pnina, Langevitz, Avi, Livneh   +3 more
openaire   +2 more sources

On demand use of anakinra for attacks of familial Mediterranean fever (FMF)

Clinical Rheumatology, 2018
To evaluate the efficacy of on-demand use of anakinra in patients with crFMF. The Gazi FMF cohort was established in the year 2010, and from that date, 689 patients with FMF diagnosed according to the Tel Hashomer criteria were registered. Attack type, duration, severity, and their impact on life were collected either by disease diaries or a mobile ...
Hakan Babaoglu, Ozkan Varan, Hamit Kucuk, Nuh Atas, Hasan Satis, Reyhan Salman, Mehmet Akif Ozturk, Seminur Haznedaroglu, Berna Goker, Abdurrahman Tufan   +9 more
openaire   +4 more sources

Genetic marker family studies in familial Mediterranean fever (FMF) in Armenians

Clinical Genetics, 1990
Familial Mediterranean fever is an autosomal recessive disease manifested by recurrent short episodes of fever associated with polyserositis. It is common in a variety of Mediterranean and near Eastern populations. The biochemical defect is unknown, and there have been few studies of genetic marker associations or linkage with the disease.
T, Shohat, M, Shohat, G M, Petersen, R S, Sparkes, D, Langfield, J, Bickal, J R, Korenberg, A D, Schwabe, J I, Rotter   +8 more
openaire   +2 more sources

Genetics of Familial Mediterranean Fever (FMF)

Archives of Internal Medicine, 1961
Introduction It has been stated in former papers1,2that Familial Mediterranean Fever (FMF) is a genetic disorder practically restricted to people from the wider Mediterranean area. This being of basic importance in the understanding of the disease and in research as to its nature, it is pertinent to report the results of a country-wide investigation ...
openaire   +1 more source