Siciliano G - Search Results

1

A new truncating MPZ mutation associated with a very mild CMT1 B phenotype.

Piazza S, Baldinotti F, Fogli A, Conidi ME, Michelucci A, Ienco EC, Mancuso M, Simi P, Siciliano G. Piazza S, et al. Among authors: siciliano g. Neuromuscul Disord. 2010 Dec;20(12):817-9. doi: 10.1016/j.nmd.2010.08.003. Epub 2010 Sep 17. Neuromuscul Disord. 2010. PMID: 20850974

2

Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 families.

Mariotti C, Castellotti B, Pareyson D, Testa D, Eoli M, Antozzi C, Silani V, Marconi R, Tezzon F, Siciliano G, Marchini C, Gellera C, Donato SD. Mariotti C, et al. Among authors: siciliano g. Neuromuscul Disord. 2000 Aug;10(6):391-7. doi: 10.1016/s0960-8966(99)00132-7. Neuromuscul Disord. 2000. PMID: 10899444

3

Cytochrome c oxidase and mitochondrial F1F0-ATPase (ATP synthase) activities in platelets and brain from patients with Alzheimer's disease.

Bosetti F, Brizzi F, Barogi S, Mancuso M, Siciliano G, Tendi EA, Murri L, Rapoport SI, Solaini G. Bosetti F, et al. Among authors: siciliano g. Neurobiol Aging. 2002 May-Jun;23(3):371-6. doi: 10.1016/s0197-4580(01)00314-1. Neurobiol Aging. 2002. PMID: 11959398

4

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. Mol Med. 2002 Jun;8(6):326-33. Mol Med. 2002. PMID: 12428064 Free PMC article.

5

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: siciliano g. Mol Med. 2002 Dec;8(12):841-6. Mol Med. 2002. PMID: 12606819 Free PMC article.

6

A screening for superoxide dismutase-1 D90A mutation in Italian patients with sporadic amyotrophic lateral sclerosis.

Mancuso M, Filosto M, Naini A, Rocchi A, Del Corona A, Sartucci F, Siciliano G, Murri L. Mancuso M, et al. Among authors: siciliano g. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002 Dec;3(4):215-8. doi: 10.1080/146608202760839007. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002. PMID: 12710511

7

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: siciliano g. Exp Neurol. 2003 Aug;182(2):421-6. doi: 10.1016/s0014-4886(03)00092-x. Exp Neurol. 2003. PMID: 12895452 Clinical Trial.

8

Proton MR spectroscopy of mitochondrial diseases: analysis of brain metabolic abnormalities and their possible diagnostic relevance.

Bianchi MC, Tosetti M, Battini R, Manca ML, Mancuso M, Cioni G, Canapicchi R, Siciliano G. Bianchi MC, et al. Among authors: siciliano g. AJNR Am J Neuroradiol. 2003 Nov-Dec;24(10):1958-66. AJNR Am J Neuroradiol. 2003. PMID: 14625217 Free PMC article.

9

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: siciliano g. Neurosci Lett. 2004 Nov 23;371(2-3):158-62. doi: 10.1016/j.neulet.2004.08.060. Neurosci Lett. 2004. PMID: 15519748

10

Cx26 gene mutations in idiopathic progressive hearing loss.

Ravecca F, Berrettini S, Forli F, Marcaccini M, Casani A, Baldinotti F, Fogli A, Siciliano G, Simi P. Ravecca F, et al. Among authors: siciliano g. J Otolaryngol. 2005 Apr;34(2):126-34. doi: 10.2310/7070.2005.04017. J Otolaryngol. 2005. PMID: 16076412

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