L. Bucchi

Protonophoric activity of NADH coenzyme Q reductase and ATP synthase in coupled submitochondrial particles from horse platelets.

A. Ghelli, A. Baracca, G. Lenaz, 1997, Biochemical and biophysical research communications.

Dominant Optic Atrophy (DOA) and Sensorineural Hearing Loss: Clinical, Biochemical, Spectroscopic and Molecular Genetic Study of a Large Italian Pedigree Linked to a New Locus on Chromosome 16

B. Barbiroli, P. Barboni, R. Lodi, 2007 .

A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16.

P. Barboni, R. Lodi, R. Youle, 2011, Human molecular genetics.

The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy.

B. Barbiroli, A. Torroni, P. Barboni, 2005, Annals of neurology.

The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy

B. Barbiroli, A. Torroni, P. Barboni, 2004 .

Biochemical features of mtDNA 14484 (ND6/m64V) point mutation associated with Leber's hereditary optic neuropathy

A. Ghelli, V. Carelli, G. Lenaz, 1999, Annals of neurology.

Respiratory function in cybrid cell lines carrying European mtDNA haplogroups: implications for Leber's hereditary optic neuropathy.

A. Torroni, C. Rengo, A. Martinuzzi, 2002, Biochimica et biophysica acta.