Arthur P. Hays

Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.

S. Dimauro, F. Santorelli, L. Vilarinho, 1997, Biochemical and biophysical research communications.

Ubiquitin expression in acute steroid myopathy with loss of myosin thick filaments

M. Pedemonte, G. Cordone, Arthur P. Hays, 1996, Muscle & nerve.

Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation.

S. Dimauro, F. Santorelli, C. Casali, 1999, American journal of human genetics.

Clinical syndromes associated with ragged red fibers.

E. Schon, L. Rowland, D. Blake, 1991, Revue neurologique.