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816 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: mancuso m. 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: mancuso m. Funct Neurol. 2000 Oct-Dec;15(4):211-4. Funct Neurol. 2000. PMID: 11213524
Sudden bilateral hearing loss and sporadic mitochondrial DNA deletion.
Berrettini S, Forli F, Siciliano G, Mancuso M. Berrettini S, et al. Among authors: mancuso m. J Laryngol Otol. 2001 Feb;115(2):128-31. doi: 10.1258/0022215011907514. J Laryngol Otol. 2001. PMID: 11320830
Cytogenetic damage in peripheral lymphocytes of mitochondrial disease patients.
Naccarati A, Molinu S, Mancuso M, Siciliano G, Migliore L. Naccarati A, et al. Among authors: mancuso m. Neurol Sci. 2000;21(5 Suppl):S963-5. doi: 10.1007/s100720070010. Neurol Sci. 2000. PMID: 11382196
Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathies.
Siciliano G, Mancuso M, Pasquali L, Manca ML, Tessa A, Iudice A. Siciliano G, et al. Among authors: mancuso m. Neurol Sci. 2000;21(5 Suppl):S985-7. doi: 10.1007/s100720070017. Neurol Sci. 2000. PMID: 11382203
Mitochondrial DNA rearrangements in young onset parkinsonism: two case reports.
Siciliano G, Mancuso M, Ceravolo R, Lombardi V, Iudice A, Bonuccelli U. Siciliano G, et al. Among authors: mancuso m. J Neurol Neurosurg Psychiatry. 2001 Nov;71(5):685-7. doi: 10.1136/jnnp.71.5.685. J Neurol Neurosurg Psychiatry. 2001. PMID: 11606686 Free PMC article.
Coenzyme Q10, exercise lactate and CTG trinucleotide expansion in myotonic dystrophy.
Siciliano G, Mancuso M, Tedeschi D, Manca ML, Renna MR, Lombardi V, Rocchi A, Martelli F, Murri L. Siciliano G, et al. Among authors: mancuso m. Brain Res Bull. 2001 Oct-Nov 1;56(3-4):405-10. doi: 10.1016/s0361-9230(01)00653-0. Brain Res Bull. 2001. PMID: 11719279
Human mitochondrial transcription factor A reduction and mitochondrial dysfunction in Hashimoto's hypothyroid myopathy.
Siciliano G, Monzani F, Manca ML, Tessa A, Caraccio N, Tozzi G, Piemonte F, Mancuso M, Santorelli FM, Ferrannini E, Murri L. Siciliano G, et al. Among authors: mancuso m. Mol Med. 2002 Jun;8(6):326-33. Mol Med. 2002. PMID: 12428064 Free PMC article.
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: mancuso m. Mol Med. 2002 Dec;8(12):841-6. Mol Med. 2002. PMID: 12606819 Free PMC article.
Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene.
Mancuso M, Filosto M, Stevens JC, Patterson M, Shanske S, Krishna S, DiMauro S. Mancuso M, et al. J Neurol Sci. 2003 May 15;209(1-2):61-3. doi: 10.1016/s0022-510x(02)00462-8. J Neurol Sci. 2003. PMID: 12686403
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