S. Didonato

发表

Carnitine in muscle, serum, and urine of nonprofessional athletes: Effects of physical exercise, training, and L‐carnitine administration

M. Zeviani, J. Arenas, S. Didonato, 1991, Muscle & nerve.

Errors in Huntington disease diagnostic test caused by trinucleotide deletion in the IT15 gene.

B. Castellotti, C. Gellera, F. Taroni, 1996, American journal of human genetics.

Primary carnitine deficiency

G. Uziel, B. Garavaglia, F. Carrara, 1991, Neurology.

Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesis.

M. Rocchi, V. Tiranti, M. Zeviani, 1995, Genomics.

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)

V. Tiranti, M. Zeviani, F. Villani, 1991, The Lancet.

Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease.

N. Bresolin, M. Zeviani, C. Gellera, 1990, American journal of human genetics.

Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF).

N. Bresolin, M. Zeviani, A. Toscano, 1991, American journal of human genetics.

Cloning of human and rat cDNAs encoding the mitochondrial single-stranded DNA-binding protein (SSB).

M. Rocchi, V. Tiranti, M. Zeviani, 1993, Gene.

Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho degrees transformants.

V. Tiranti, M. Zeviani, E. Lamantea, 1995, Human molecular genetics.

A full-length cDNA encoding a mitochondrial DNA-specific single-stranded DNA binding protein from Xenopus laevis.

V. Tiranti, M. Zeviani, J. Bijl, 1991, Nucleic acids research.

Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies

M. Zeviani, G. Uziel, A. Prelle, 1990, Annals of neurology.

Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNA(Leu(UUR)) mutation associated with maternally inherited myopathy and cardiomyopathy.

V. Tiranti, M. Zeviani, B. Dallapiccola, 1994, The Journal of clinical investigation.

Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymes

M. Zeviani, C. Gellera, G. Uziel, 1990, Neurology.

Concordance of Clinical Forms of Epilepsy in Families with Several Affected Members

M. Manfredi, G. Avanzini, R. Massetani, 1993, Epilepsia.

Sequence analysis of mitochondrial DNA in a new maternally inherited encephalomyopathy

V. Tiranti, M. Zeviani, G. Guazzi, 1995, Journal of Neurology.

Underestimation of ovarian pathology: a review.

M. Pellicano, M. Guida, V. Napolitano, 1997, Journal of chemotherapy.