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Page 1
Oxidative Stress Assessment in Alzheimer's Disease: A Clinic Setting Study.
Vergallo A, Giampietri L, Baldacci F, Volpi L, Chico L, Pagni C, Giorgi FS, Ceravolo R, Tognoni G, Siciliano G, Bonuccelli U. Vergallo A, et al. Among authors: volpi l. Am J Alzheimers Dis Other Demen. 2018 Feb;33(1):35-41. doi: 10.1177/1533317517728352. Epub 2017 Sep 21. Am J Alzheimers Dis Other Demen. 2018. PMID: 28931301 Free PMC article.
Functional diagnostics in mitochondrial diseases.
Siciliano G, Volpi L, Piazza S, Ricci G, Mancuso M, Murri L. Siciliano G, et al. Among authors: volpi l. Biosci Rep. 2007 Jun;27(1-3):53-67. doi: 10.1007/s10540-007-9037-0. Biosci Rep. 2007. PMID: 17492503 Review.
Astrocyte-neuron interactions in neurological disorders.
Ricci G, Volpi L, Pasquali L, Petrozzi L, Siciliano G. Ricci G, et al. Among authors: volpi l. J Biol Phys. 2009 Oct;35(4):317-36. doi: 10.1007/s10867-009-9157-9. Epub 2009 May 14. J Biol Phys. 2009. PMID: 19669420 Free PMC article.
Coenzyme Q10 in neuromuscular and neurodegenerative disorders.
Mancuso M, Orsucci D, Volpi L, Calsolaro V, Siciliano G. Mancuso M, et al. Among authors: volpi l. Curr Drug Targets. 2010 Jan;11(1):111-21. doi: 10.2174/138945010790031018. Curr Drug Targets. 2010. PMID: 20017723 Review.
Serum gamma-glutamyltransferase fractions in myotonic dystrophy type I: differences with healthy subjects and patients with liver disease.
Franzini M, Fornaciari I, Siciliano G, Volpi L, Ricci G, Marchi S, Gagliardi G, Baggiani A, Torracca F, Fierabracci V, Miccoli M, Pompella A, Emdin M, Paolicchi A. Franzini M, et al. Among authors: volpi l. Clin Biochem. 2010 Oct;43(15):1246-8. doi: 10.1016/j.clinbiochem.2010.07.018. Epub 2010 Aug 4. Clin Biochem. 2010. PMID: 20691173
Pes cavus and hereditary neuropathies: when a relationship should be suspected.
Piazza S, Ricci G, Caldarazzo Ienco E, Carlesi C, Volpi L, Siciliano G, Mancuso M. Piazza S, et al. Among authors: volpi l. J Orthop Traumatol. 2010 Dec;11(4):195-201. doi: 10.1007/s10195-010-0114-y. Epub 2010 Oct 21. J Orthop Traumatol. 2010. PMID: 20963465 Free PMC article. Review.
Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromes.
Ricci G, Scionti I, Alì G, Volpi L, Zampa V, Fanin M, Angelini C, Politano L, Tupler R, Siciliano G. Ricci G, et al. Among authors: volpi l. Neuromuscul Disord. 2012 Jun;22(6):534-40. doi: 10.1016/j.nmd.2011.12.001. Epub 2012 Jan 14. Neuromuscul Disord. 2012. PMID: 22245016 Free PMC article.
155 results