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279 results
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Functional diagnostics in mitochondrial diseases.
Siciliano G, Volpi L, Piazza S, Ricci G, Mancuso M, Murri L. Siciliano G, et al. Among authors: murri l. Biosci Rep. 2007 Jun;27(1-3):53-67. doi: 10.1007/s10540-007-9037-0. Biosci Rep. 2007. PMID: 17492503 Review.
Abnormal H-Tfam in a patient harboring a single mtDNA deletion.
Tessa A, Manca ML, Mancuso M, Renna MR, Murri L, Martini B, Santorelli FM, Siciliano G. Tessa A, et al. Among authors: murri l. Funct Neurol. 2000 Oct-Dec;15(4):211-4. Funct Neurol. 2000. PMID: 11213524
Genes and the environment in neurodegeneration.
Coppedè F, Mancuso M, Siciliano G, Migliore L, Murri L. Coppedè F, et al. Among authors: murri l. Biosci Rep. 2006 Oct;26(5):341-67. doi: 10.1007/s10540-006-9028-6. Biosci Rep. 2006. PMID: 17029001 Review.
Association of the hOGG1 Ser326Cys polymorphism with sporadic amyotrophic lateral sclerosis.
Coppedè F, Mancuso M, Lo Gerfo A, Carlesi C, Piazza S, Rocchi A, Petrozzi L, Nesti C, Micheli D, Bacci A, Migliore L, Murri L, Siciliano G. Coppedè F, et al. Among authors: murri l. Neurosci Lett. 2007 Jun 13;420(2):163-8. doi: 10.1016/j.neulet.2007.04.067. Epub 2007 May 5. Neurosci Lett. 2007. PMID: 17531381
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis?
Mancuso M, Conforti FL, Rocchi A, Tessitore A, Muglia M, Tedeschi G, Panza D, Monsurrò M, Sola P, Mandrioli J, Choub A, DelCorona A, Manca ML, Mazzei R, Sprovieri T, Filosto M, Salviati A, Valentino P, Bono F, Caracciolo M, Simone IL, La Bella V, Majorana G, Siciliano G, Murri L, Quattrone A. Mancuso M, et al. Among authors: murri l. Neurosci Lett. 2004 Nov 23;371(2-3):158-62. doi: 10.1016/j.neulet.2004.08.060. Neurosci Lett. 2004. PMID: 15519748
Autosomal dominant psychiatric disorders and mitochondrial DNA multiple deletions: report of a family.
Mancuso M, Ricci G, Choub A, Filosto M, DiMauro S, Davidzon G, Tessa A, Santorelli FM, Murri L, Siciliano G. Mancuso M, et al. Among authors: murri l. J Affect Disord. 2008 Feb;106(1-2):173-7. doi: 10.1016/j.jad.2007.05.016. Epub 2007 Jun 22. J Affect Disord. 2008. PMID: 17588675
Mitochondrial dysfunction and Alzheimer's disease: new developments.
Mancuso M, Siciliano G, Filosto M, Murri L. Mancuso M, et al. Among authors: murri l. J Alzheimers Dis. 2006 Jul;9(2):111-7. doi: 10.3233/jad-2006-9203. J Alzheimers Dis. 2006. PMID: 16873958 Review.
Mitochondrial dysfunction, oxidative stress and neurodegeneration.
Mancuso M, Coppede F, Migliore L, Siciliano G, Murri L. Mancuso M, et al. Among authors: murri l. J Alzheimers Dis. 2006 Sep;10(1):59-73. doi: 10.3233/jad-2006-10110. J Alzheimers Dis. 2006. PMID: 16988483 Review.
Decreased platelet cytochrome c oxidase activity is accompanied by increased blood lactate concentration during exercise in patients with Alzheimer disease.
Mancuso M, Filosto M, Bosetti F, Ceravolo R, Rocchi A, Tognoni G, Manca ML, Solaini G, Siciliano G, Murri L. Mancuso M, et al. Among authors: murri l. Exp Neurol. 2003 Aug;182(2):421-6. doi: 10.1016/s0014-4886(03)00092-x. Exp Neurol. 2003. PMID: 12895452 Clinical Trial.
Peripheral benzodiazepine binding sites in platelets of patients affected by mitochondrial diseases and large scale mitochondrial DNA rearrangements.
Martini C, Chelli B, Betti L, Montali M, Mancuso M, Giannaccini G, Rocchi A, Murri L, Siciliano G. Martini C, et al. Among authors: murri l. Mol Med. 2002 Dec;8(12):841-6. Mol Med. 2002. PMID: 12606819 Free PMC article.
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