Mancuso M - Search Results

1

Biomolecules of Muscle Fatigue in Metabolic Myopathies.

Schirinzi E, Ricci G, Torri F, Mancuso M, Siciliano G. Schirinzi E, et al. Among authors: mancuso m. Biomolecules. 2023 Dec 30;14(1):50. doi: 10.3390/biom14010050. Biomolecules. 2023. PMID: 38254650 Free PMC article. Review.

2

Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitation.

Siciliano G, Tessa A, Renna M, Manca ML, Mancuso M, Murri L. Siciliano G, et al. Among authors: mancuso m. Clin Genet. 1999 Jul;56(1):51-8. doi: 10.1034/j.1399-0004.1999.560107.x. Clin Genet. 1999. PMID: 10466417

3

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

4

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

5

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

6

Potential involvement of ubiquinone in myotonic dystrophy pathophysiology: new diagnostic approaches for new rationale therapeutics.

Tedeschi D, Lombardi V, Mancuso M, Martelli F, Sighieri C, Rocchi A, Tovani S, Siciliano G, Murri L. Tedeschi D, et al. Among authors: mancuso m. Neurol Sci. 2000;21(5 Suppl):S979-80. doi: 10.1007/s100720070014. Neurol Sci. 2000. PMID: 11382200

7

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

8

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.

9

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

10

Dissection and atherosclerosis of carotid arteries in the young: role of the apolipoprotein E polymorphism.

Orlandi G, Fanucchi S, Mancuso M, Gelli A, Rocchi A, Siciliano G, Murri L. Orlandi G, et al. Among authors: mancuso m. Eur J Neurol. 2002 Jan;9(1):19-21. doi: 10.1046/j.1468-1331.2002.00340.x. Eur J Neurol. 2002. PMID: 11784371

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