[Polymyositis during adult-onset Still's disease]. 2004

G Defuentes, and S Lecoules, and J Desramé, and G Coutant, and J-P Algayres

UI MeSH Term Description Entries
D008297 Male Males
D004576 Electromyography Recording of the changes in electric potential of muscle by means of surface or needle electrodes. Electromyogram,Surface Electromyography,Electromyograms,Electromyographies,Electromyographies, Surface,Electromyography, Surface,Surface Electromyographies
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D016706 Still's Disease, Adult-Onset Systemic-onset rheumatoid arthritis in adults. It differs from classical rheumatoid arthritis in that it is more often marked by acute febrile onset, and generalized lymphadenopathy and hepatosplenomegaly are more prominent. Adult-Onset Still Disease,Adult-Onset Still's Disease,Still Disease, Adult-Onset,Adult Onset Still Disease,Adult Onset Still's Disease,Adult-Onset Stills Disease,Still Disease, Adult Onset,Still's Disease, Adult Onset,Stills Disease, Adult-Onset
D017285 Polymyositis Diseases characterized by inflammation involving multiple muscles. This may occur as an acute or chronic condition associated with medication toxicity (DRUG TOXICITY); CONNECTIVE TISSUE DISEASES; infections; malignant NEOPLASMS; and other disorders. The term polymyositis is frequently used to refer to a specific clinical entity characterized by subacute or slowly progressing symmetrical weakness primarily affecting the proximal limb and trunk muscles. The illness may occur at any age, but is most frequent in the fourth to sixth decade of life. Weakness of pharyngeal and laryngeal muscles, interstitial lung disease, and inflammation of the myocardium may also occur. Muscle biopsy reveals widespread destruction of segments of muscle fibers and an inflammatory cellular response. (Adams et al., Principles of Neurology, 6th ed, pp1404-9) Myositis, Multiple,Polymyositis Ossificans,Polymyositis, Idiopathic,Idiopathic Polymyositides,Idiopathic Polymyositis,Multiple Myositis,Myositides, Multiple,Ossificans, Polymyositis,Polymyositides,Polymyositides, Idiopathic

Related Publications

G Defuentes, and S Lecoules, and J Desramé, and G Coutant, and J-P Algayres
September 2006, Praxis,
G Defuentes, and S Lecoules, and J Desramé, and G Coutant, and J-P Algayres
July 1995, International journal of dermatology,
G Defuentes, and S Lecoules, and J Desramé, and G Coutant, and J-P Algayres
March 2008, Revue medicale suisse,
G Defuentes, and S Lecoules, and J Desramé, and G Coutant, and J-P Algayres
October 2004, Best practice & research. Clinical rheumatology,
G Defuentes, and S Lecoules, and J Desramé, and G Coutant, and J-P Algayres
May 1976, American family physician,
G Defuentes, and S Lecoules, and J Desramé, and G Coutant, and J-P Algayres
March 1985, New York state journal of medicine,
G Defuentes, and S Lecoules, and J Desramé, and G Coutant, and J-P Algayres
January 2006, Annales Academiae Medicae Stetinensis,
G Defuentes, and S Lecoules, and J Desramé, and G Coutant, and J-P Algayres
June 1995, Medizinische Klinik (Munich, Germany : 1983),
G Defuentes, and S Lecoules, and J Desramé, and G Coutant, and J-P Algayres
September 2016, Medicina clinica,
G Defuentes, and S Lecoules, and J Desramé, and G Coutant, and J-P Algayres
May 2018, Medicina clinica,
Copied contents to your clipboard!