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Italian Journal of Pediatrics|April 9, 2014
Syndromes associated with mitochondrial DNA depletionCélia Nogueira, Ligia S Almeida, Claudia Nesti, et al.Journal of Cellular Biochemistry|January 23, 2009
Cellular and functional analysis of four mutations located in the mitochondrial ATPase6 geneMartha Elisa Vazquez-Memije, Teresa Rizza, Maria Chiara Meschini, et al.Neurogenetics|January 26, 2019
Clinical and molecular studies in two new cases of ARSACSIvana Ricca, Federica Morani, Giacomo Maria Bacci, et al.Brain Research|September 22, 2010
Human dental pulp stem cells protect mouse dopaminergic neurons against MPP+ or rotenoneClaudia Nesti, Carla Pardini, Serena Barachini, et al.The American Journal of Medicine|June 24, 2004
Thyroid disorders in chronic hepatitis CAlessandro Antonelli, Clodoveo Ferri, Alessandro Pampana, et al.Journal of Molecular and Cellular Cardiology|May 26, 2005
Novel cell lines derived from adult human ventricular cardiomyocytesMercy M Davidson, Claudia Nesti, Lluis Palenzuela, et al.Biomedical Materials (Bristol, England)|July 17, 2014
Processing large-diameter poly(L-lactic acid) microfiber mesh/mesenchymal stromal cell constructs via resin embedding: an efficient histologic methodDelfo D'Alessandro, Gianni Pertici, Stefania Moscato, et al.Molecular Genetics and Metabolism Reports|March 26, 2016
A novel mitochondrial tRNA(Ala) gene variant causes chronic progressive external ophthalmoplegia in a patient with Huntington diseaseMassimiliano Filosto, Gaetana Lanzi, Claudia Nesti, et al.BMC Medical Genomics|January 22, 2021
Leopard-like retinopathy and severe early-onset portal hypertension expand the phenotype of KARS1-related syndrome: a case reportFrancesca Peluso, Viviana Palazzo, Giuseppe Indolfi, et al.Archives of Neurology|December 15, 2004
Studies of COX16, COX19, and PET191 in human cytochrome-c oxidase deficiencyStacey K H Tay, Claudia Nesti, Michelangelo Mancuso, et al.Pageof 7