Siciliano G - Search Results

1

Mitochondrial DNA haplogroups may influence Fabry disease phenotype.

Simoncini C, Chico L, Concolino D, Sestito S, Fancellu L, Boadu W, Sechi GP, Feliciani C, Gnarra M, Zampetti A, Salviati A, Scarpelli M, Orsucci D, Bonuccelli U, Siciliano G, Mancuso M. Simoncini C, et al. Among authors: siciliano g. Neurosci Lett. 2016 Aug 26;629:58-61. doi: 10.1016/j.neulet.2016.06.051. Epub 2016 Jun 27. Neurosci Lett. 2016. PMID: 27365132

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. Clin Genet. 1999 Jul;56(1):51-8. doi: 10.1034/j.1399-0004.1999.560107.x. Clin Genet. 1999. PMID: 10466417

3

Encephalomyopathy with multiple mitochondrial DNA deletions and multiple symmetric lipomatosis: further evidence of a possible association.

Mancuso M, Bianchi MC, Santorelli FM, Tessa A, Casali C, Murri L, Siciliano G. Mancuso M, et al. Among authors: siciliano g. J Neurol. 1999 Dec;246(12):1197-8. doi: 10.1007/s004150050543. J Neurol. 1999. PMID: 10653316 No abstract available.

4

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: siciliano g. Funct Neurol. 2000 Oct-Dec;15(4):211-4. Funct Neurol. 2000. PMID: 11213524

5

Sudden bilateral hearing loss and sporadic mitochondrial DNA deletion.

Berrettini S, Forli F, Siciliano G, Mancuso M. Berrettini S, et al. Among authors: siciliano g. J Laryngol Otol. 2001 Feb;115(2):128-31. doi: 10.1258/0022215011907514. J Laryngol Otol. 2001. PMID: 11320830

6

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: siciliano g. Neurol Sci. 2000;21(5 Suppl):S963-5. doi: 10.1007/s100720070010. Neurol Sci. 2000. PMID: 11382196

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. 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. 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. 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: siciliano g. 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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