| Sarcopenia: aging-related loss of muscle mass and function L Larsson, H Degens, M Li, L Salviati, YI Lee, W Thompson, JL Kirkland, ... Physiological reviews 99 (1), 427-511, 2019 | 1456 | 2019 |
| Mitochondrial cristae shape determines respiratory chain supercomplexes assembly and respiratory efficiency S Cogliati, C Frezza, ME Soriano, T Varanita, R Quintana-Cabrera, ... Cell 155 (1), 160-171, 2013 | 1302 | 2013 |
| Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells M Spinazzi, A Casarin, V Pertegato, L Salviati, C Angelini Nature protocols 7 (6), 1235-1246, 2012 | 1053 | 2012 |
| Age-associated loss of OPA1 in muscle impacts muscle mass, metabolic homeostasis, systemic inflammation, and epithelial senescence C Tezze, V Romanello, MA Desbats, GP Fadini, M Albiero, G Favaro, ... Cell metabolism 25 (6), 1374-1389. e6, 2017 | 546 | 2017 |
| COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness SF Heeringa, G Chernin, M Chaki, W Zhou, AJ Sloan, Z Ji, LX Xie, ... The Journal of clinical investigation 121 (5), 2013-2024, 2011 | 440 | 2011 |
| A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency C Quinzii, A Naini, L Salviati, E Trevisson, P Navas, S DiMauro, M Hirano The American Journal of Human Genetics 78 (2), 345-349, 2006 | 406 | 2006 |
| ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption S Ashraf, HY Gee, S Woerner, LX Xie, V Vega-Warner, S Lovric, H Fang, ... The Journal of clinical investigation 123 (12), 5179-5189, 2013 | 385 | 2013 |
| DRP1-mediated mitochondrial shape controls calcium homeostasis and muscle mass G Favaro, V Romanello, T Varanita, M Andrea Desbats, V Morbidoni, ... Nature communications 10 (1), 2576, 2019 | 376 | 2019 |
| Mitochondrial dysfunction in inherited renal disease and acute kidney injury F Emma, G Montini, SM Parikh, L Salviati Nature Reviews Nephrology 12 (5), 267-280, 2016 | 369 | 2016 |
| Coenzyme Q biosynthesis in health and disease MJ Acosta, LV Fonseca, MA Desbats, C Cerqua, R Zordan, E Trevisson, ... Biochimica et Biophysica Acta (BBA)-Bioenergetics 1857 (8), 1079-1085, 2016 | 284 | 2016 |
| Early coenzyme Q10 supplementation in primary coenzyme Q10 deficiency G Montini, C Malaventura, L Salviati New England Journal of Medicine 358 (26), 2849-2850, 2008 | 283 | 2008 |
| Genetic bases and clinical manifestations of coenzyme Q10 (CoQ10) deficiency MA Desbats, G Lunardi, M Doimo, E Trevisson, L Salviati Journal of inherited metabolic disease 38, 145-156, 2015 | 259 | 2015 |
| Coenzyme Q deficiency triggers mitochondria degradation by mitophagy Á Rodríguez-Hernández, MD Cordero, L Salviati, R Artuch, M Pineda, ... Autophagy 5 (1), 19-32, 2009 | 243 | 2009 |
| Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive condition L Salviati, S Sacconi, L Murer, G Zacchello, L Franceschini, AM Laverda, ... Neurology 65 (4), 606-608, 2005 | 226 | 2005 |
| The FSHD2 gene SMCHD1 is a modifier of disease severity in families affected by FSHD1 S Sacconi, RJLF Lemmers, J Balog, PJ van Der Vliet, P Lahaut, ... The American Journal of Human Genetics 93 (4), 744-751, 2013 | 214 | 2013 |
| LETM1, deleted in Wolf–Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viability KS Dimmer, F Navoni, A Casarin, E Trevisson, S Endele, A Winterpacht, ... Human molecular genetics 17 (2), 201-214, 2008 | 213 | 2008 |
| Newborn screening for lysosomal storage disorders by tandem mass spectrometry in North East Italy AB Burlina, G Polo, L Salviati, G Duro, C Zizzo, A Dardis, B Bembi, ... Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2018 | 192 | 2018 |
| Reactive oxygen species, oxidative stress, and cell death correlate with level of CoQ10 deficiency CM Quinzii, LC López, RW Gilkerson, B Dorado, J Coku, AB Naini, ... The FASEB Journal 24 (10), 3733, 2010 | 191 | 2010 |
| Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency CM Quinzii, LC López, J Von-Moltke, A Naini, S Krishna, M Schuelke, ... The FASEB journal: official publication of the Federation of American …, 2008 | 190 | 2008 |
| Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA M Mancuso, L Salviati, S Sacconi, D Otaegui, P Camano, A Marina, ... Neurology 59 (8), 1197-1202, 2002 | 189 | 2002 |
