M Mirabella

Difference in Expression of Phosphorylated Tau Epitopes between Sporadic Inclusion‐body Myositis and Hereditary Inclusion‐body Myopathies

W. Engel, M. Mirabella, V. Askanas, 1996, Journal of neuropathology and experimental neurology.

Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophy

E. Bertini, P. Tonali, E. Ricci, 1998, Neurology.

Idiopathic inflammatory myopathies: inclusion‐body myositis, polymyositis, and dermatomyositis

W. Engel, M. Mirabella, V. Askanas, 1994, Current opinion in neurology.

Coenzyme Q10 reverses pathological phenotype and reduces apoptosis in familial CoQ10 deficiency

S. Di Giovanni, P. Tonali, A. Broccolini, 2001, Neurology.