| Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA AL Andreu, MG Hanna, H Reichmann, C Bruno, AS Penn, K Tanji, ... New England Journal of Medicine 341 (14), 1037-1044, 1999 | 491 | 1999 |
| Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy J Guy, X Qi, F Pallotti, EA Schon, G Manfredi, V Carelli, A Martinuzzi, ... Annals of Neurology: Official Journal of the American Neurological …, 2002 | 305 | 2002 |
| Isolation and subfractionation of mitochondria from animal cells and tissue culture lines F Pallotti, G Lenaz Methods in cell biology 65, 1-35, 2001 | 300* | 2001 |
| Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees V Carelli, A Achilli, ML Valentino, C Rengo, O Semino, M Pala, A Olivieri, ... The American journal of human genetics 78 (4), 564-574, 2006 | 229 | 2006 |
| Assay conditions for the mitochondrial NADH: coenzyme Q oxidoreductase E Estornell, R Fato, F Pallotti, G Lenaz FEBS letters 332 (1-2), 127-131, 1993 | 220 | 1993 |
| Mitochondrial complex I defects in aging G Lenaz, C Bovina, C Castelluccio, R Fato, G Formiggini, ML Genova, ... Detection of Mitochondrial Diseases, 329-333, 1997 | 191 | 1997 |
| Steady-state kinetics of the reduction of coenzyme Q analogs by complex I (NADH: ubiquinone oxidoreductase) in bovine heart mitochondria and submitochondrial particles R Fato, E Estornell, S Di Bernardo, F Pallotti, G Parenti Castelli, G Lenaz Biochemistry 35 (8), 2705-2716, 1996 | 178 | 1996 |
| A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV C Bruno, A Martinuzzi, Y Tang, AL Andreu, F Pallotti, E Bonilla, S Shanske, ... The American Journal of Human Genetics 65 (3), 611-620, 1999 | 175 | 1999 |
| Isolation and subfractionation of mitochondria from animal cells and tissue culture lines F Pallotti, G Lenaz Methods in cell biology 65, 1-35, 2001 | 157 | 2001 |
| Differential features of patients with mutations in two COX assembly genes, SURF‐1 and SCO2 CM Sue, C Karadimas, N Checcarelli, K Tanji, LC Papadopoulou, ... Annals of neurology 47 (5), 589-595, 2000 | 152 | 2000 |
| Isolation and subfractionation of mitochondria from animal cells and tissue culture lines F Pallotti, G Lenaz Methods in cell biology 80, 3-44, 2007 | 148 | 2007 |
| Pathogenesis of primary defects in mitochondrial ATP synthesis EA Schon, S Santra, F Pallotti, ME Girvin Seminars in cell & developmental biology 12 (6), 441-448, 2001 | 143 | 2001 |
| The fate of human sperm-derived mtDNA in somatic cells G Manfredi, D Thyagarajan, LC Papadopoulou, F Pallotti, EA Schon The American Journal of Human Genetics 61 (4), 953-960, 1997 | 135 | 1997 |
| Molecular cloning and characterization of UDP-glucose dehydrogenase from the amphibian Xenopus laevis and its involvement in hyaluronan synthesis D Vigetti, M Ori, M Viola, A Genasetti, E Karousou, M Rizzi, F Pallotti, ... Journal of Biological Chemistry 281 (12), 8254-8263, 2006 | 127 | 2006 |
| Evidence that specific mtDNA point mutations may not accumulate in skeletal muscle during normal human aging. F Pallotti, XI Chen, E Bonilla, EA Schon American journal of human genetics 59 (3), 591, 1996 | 121 | 1996 |
| Hyaluronan and human endothelial cell behavior A Genasetti, D Vigetti, M Viola, E Karousou, P Moretto, M Rizzi, B Bartolini, ... Connective Tissue Research 49 (3-4), 120-123, 2008 | 104 | 2008 |
| Oxidative stress, antioxidant defences and aging G Lenaz, M Cavazzoni, ML Genova, M D'Aurelio, MM Pich, F Pallotti, ... Biofactors 8 (3‐4), 195-204, 1998 | 96 | 1998 |
| Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations F Pallotti, A Baracca, E Hernandez-Rosa, WF Walker, G Solaini, G Lenaz, ... Biochemical Journal 384 (2), 287-293, 2004 | 91 | 2004 |
| The function of coenzyme Q in mitochondria G Lenaz, R Fato, C Castelluccio, ML Genova, C Bovina, E Estornell, ... The clinical investigator 71, S66-S70, 1993 | 88 | 1993 |
| Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation V Carelli, A Baracca, S Barogi, F Pallotti, ML Valentino, P Montagna, ... Archives of neurology 59 (2), 264-270, 2002 | 83 | 2002 |
