Cátedra de Clínica Médica – Facultad de Ciencias Médicas – Universidad Nacional de Rosario

Referencias bibliográficas

1.     Briemberg H. 10 most commonly asked questions about idiopathic inflammatory myopathies. Neurologist 2005;11:250-3.

2.     Christopher-Stine L, Plotz PH. Adult inflammatory myopathies. Best Pract Res Clin Rheumatol 2004; 18:331-44.

3.     Dalakas MC. Mechanisms of disease: signaling pathways and immunobiology of inflammatory myopathies. Nat Clin Pract Rheumatol 2006;2:219-27.

4.     Gerami P, Schope JM, McDonald L, Walling HW, Sontheimer RD. A systematic review of adult-onset clinically amyopathic dermatomyositis (dermatomyositis sine myositis): a missing link within the spectrum of the idiopathic inflammatory myopathies. J Am Acad Dermatol 2006;54:597-613.

5.     Munshi SK, Thanvi B, Jonnalagadda SJ, Da Forno P, Patel A, Sharma S. Inclusion body myositis: an underdiagnosed myopathy of older people. Age Ageing 2006;35:91-4.

6.     Polisson RP, Crocker JT, Mueller PR, Harris NL, Duncan LM. Case records of the Massachusetts General Hospital. Case 29-2005. A 68-year-old man with periorbital swelling, rash, and weakness. N Engl J Med 2005;353:1275-84.

7.     Targoff IN. Myositis specific autoantibodies. Curr Rheumatol Rep 2006;8:196-203.

8.     Ytterberg SR. Treatment of refractory polymyositis and dermatomyositis. Curr Rheumatol Rep 2006;8:167-73.