Eva Trevisson

Eva Trevisson

Università degli Studi di Padova - Padova / Italy
Medical and Health Sciences / Medical Genetics
AD Scientific Index ID: 1801359
University of Padua
person_outline Eva Trevisson's MOST POPULAR ARTICLES
1-) COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafnessSF Heeringa, G Chernin, M Chaki, W Zhou, AJ Sloan, Z Ji, LX Xie, ...The Journal of clinical investigation 121 (5), 2013-2024, 20113962011
2-) A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiencyC Quinzii, A Naini, L Salviati, E Trevisson, P Navas, S DiMauro, M HiranoThe American Journal of Human Genetics 78 (2), 345-349, 20063832006
3-) Coenzyme Q biosynthesis in health and diseaseMJ Acosta, LV Fonseca, MA Desbats, C Cerqua, R Zordan, E Trevisson, ...Biochimica et Biophysica Acta (BBA)-Bioenergetics 1857 (8), 1079-1085, 20162152016
4-) Genetic bases and clinical manifestations of coenzyme Q10 (CoQ10) deficiencyMA Desbats, G Lunardi, M Doimo, E Trevisson, L SalviatiJournal of inherited metabolic disease 38, 145-156, 20152472015
5-) LETM1, deleted in Wolf–Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viabilityKS Dimmer, F Navoni, A Casarin, E Trevisson, S Endele, A Winterpacht, ...Human molecular genetics 17 (2), 201-214, 20082152008