S. Dimauro

发表

Cytochrome c Oxidase Deficiency

E. Shoubridge, H. Nakase, A. Lombès, 1990, Pediatric Research.

Clinical manifestations of mitochondria1 DNA depletion

S. Dimauro, E. Schon, D. Devivo, 1998, Neurology.

Mitochondrial defects of brain and muscle.

S. Dimauro, D. Vivo, D. D. De Vivo, 1990, Biology of the neonate.

Myophosphorylase gene transfer in McArdle’s disease myoblasts in vitro

G. Pari, E. Shoubridge, S. Dimauro, 1999, Neurology.

A novel mitochondrial tRNA mutation causes MERRF syndrome

V. Mootha, S. Dimauro, L. Murri, 2004 .

Mitochondrial DNA depletion, near-fatal metabolic acidosis, and liver failure in an HIV-infected child treated with combination antiretroviral therapy.

S. Dimauro, J. Church, R. Boles, 2001, The Journal of pediatrics.

Mitochondria1 involvement in Parkinson's disease

S. Dimauro, S. DiMauro, S. Dimauro, 1993, Neurology.

Valproic Acid Impairs Carnitine Uptake in Cultured Human Skin Fibroblasts. An In Vitro Model for the Pathogenesis of Valproic Acid–Associated Carnitine Deficiency

S. Dimauro, D. Vivo, I. Tein, 1993, Pediatric Research.

A case of acute urinary retention caused by periaqueductal grey

M. Dotti, D. Thorburn, F. Moriwaka, 2004 .