Salvatore DiMauro

Phenotype–genotype correlations in skeletal muscle of patients with mtDNA deletions

S. Dimauro, E. Schon, E. Ricci, 1995, Muscle & nerve. Supplement.

Human CoQ10 deficiencies

S. Dimauro, M. Hirano, A. Naini, 2008, BioFactors.

Mitochondrial diseases.

S. Dimauro, M. Zeviani, D. Devivo, 1989, Neurologic clinics.

Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease).

S. Dimauro, S. Tsujino, S. Shanske, 1993, The New England journal of medicine.

Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency.

S. Dimauro, R. Estabrook, R. Haller, 1989, The Journal of clinical investigation.

MELAS: Clinical features, biochemistry, and molecular genetics

S. Dimauro, E. Schon, A. Martinuzzi, 1992, Annals of neurology.

Lipid storage myopathy, ichthyosis, and steatorrhea

S. Dimauro, R. Mayeux, W. Johnson, 1979, Muscle & nerve.

A new mtDNA mutation in the tRNALeu(UUR) gene associated with maternally inherited cardiomyopathy

S. Dimauro, F. Santorelli, G. Silvestri, 1994, Human mutation.