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Annals of Neurology|October 29, 2002
Rescue of a mitochondrial deficiency causing Leber Hereditary Optic NeuropathyJohn Guy, Xiaoping Qi, Francesco Pallotti, et al.Plos One|May 9, 2014
A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneckFrancesco Pallotti, Giorgio Binelli, Raffaella Fabbri, et al.Journal of Pharmaceutical and Biomedical Analysis|November 19, 2005
Decorin from different bovine tissues: study of glycosaminoglycan chain by PAGEFSManuela Viola, Evgenia G Karousou, Davide Vigetti, et al.Connective Tissue Research|July 29, 2008
Aortic smooth muscle cells migration and the role of metalloproteinases and hyaluronanDavide Vigetti, Paola Moretto, Manuela Viola, et al.Journal of Nephrology|May 23, 2002
Renal ultrastructural findings in Anderson-Fabry diseaseAdalberto Sessa, Antonella Toson, Manuela Nebuloni, et al.Archives of Neurology|February 15, 2002
Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutationValerio Carelli, Alessandra Baracca, Silvia Barogi, et al.Connective Tissue Research|July 29, 2008
Molecular control of the hyaluronan biosynthesisManuela Viola, Davide Vigetti, Anna Genasetti, et al.The Journal of Biological Chemistry|January 19, 2006
Molecular cloning and characterization of UDP-glucose dehydrogenase from the amphibian Xenopus laevis and its involvement in hyaluronan synthesisDavide Vigetti, Michela Ori, Manuela Viola, et al.Molecular Genetics and Metabolism Reports|January 11, 2017
Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 geneAlice Zanolini, Ana Potic, Franco Carrara, et al.Plos One|September 13, 2011
Chromosomal aberrations in bladder cancer: fresh versus formalin fixed paraffin embedded tissue and targeted FISH versus wide microarray-based CGH analysisElena Panzeri, Donatella Conconi, Laura Antolini, et al.Pageof 10