MEDITERRANEAN HEMOPATHIC SYNDROMES
نویسندگان
چکیده
منابع مشابه
Polyradiculoneuritis, cryopyrin-associated periodic syndromes, and familial Mediterranean fever.
Familial Mediterranean fever (FMF) is the most common hereditary autoinflammatory disease in the world. It shows a high prevalence in countries bordering the eastern Mediterranean. The course of the disease is marked by short and self-limiting bouts of fever, often with a monthly periodicity; other clinical manifestations include serositis and synovitis. Mutations of the cold-induced autoinflam...
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INTRODUCTION So far, no studies have been performed regarding the epidemiology and management of acute coronary syndromes (ACS) in Cyprus. The aim of the present study was to enroll a representative sample of patients in order to study the epidemiology and management of ACS in the Mediterranean island of Cyprus. METHODS For a period of 12 months, all patients admitted to Nicosia General Hospi...
متن کاملLETTERS TO THE EDITOR Polyradiculoneuritis, cryopyrin-associated periodic syndromes, and familial Mediterranean fever
Familial Mediterranean fever (FMF) is the most common hereditary autoinflammatory disease in the world. It shows a high prevalence in countries bordering the eastern Mediterranean. The course of the disease is marked by short and self-limiting bouts of fever, often with a monthly periodicity; other clinical manifestations include serositis and synovitis. Mutations of the cold-induced autoinflam...
متن کاملUnified modeling of Familial Mediterranean Fever and Cryopyrin Associated Periodic Syndromes
Familial mediterranean fever (FMF) and Cryopyrin associated periodic syndromes (CAPS) are two prototypical hereditary autoinflammatory diseases, characterized by recurrent episodes of fever and inflammation as a result of mutations in MEFV and NLRP3 genes encoding Pyrin and Cryopyrin proteins, respectively. Pyrin and Cryopyrin play key roles in the multiprotein inflammasome complex assembly, wh...
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ژورنال
عنوان ژورنال: Blood
سال: 1949
ISSN: 0006-4971,1528-0020
DOI: 10.1182/blood.v4.9.989.989