Filosto M - Search Results

1

A novel mitochondrial tRNA(Ala) gene variant causes chronic progressive external ophthalmoplegia in a patient with Huntington disease.

Filosto M, Lanzi G, Nesti C, Vielmi V, Marchina E, Galvagni A, Giliani S, Santorelli FM, Padovani A. Filosto M, et al. Mol Genet Metab Rep. 2016 Feb 27;6:70-3. doi: 10.1016/j.ymgmr.2016.02.001. eCollection 2016 Mar. Mol Genet Metab Rep. 2016. PMID: 27014581 Free PMC article.

2

A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia.

Spagnolo M, Tomelleri G, Vattemi G, Filosto M, Rizzuto N, Tonin P. Spagnolo M, et al. Among authors: filosto m. Neuromuscul Disord. 2001 Jul;11(5):481-4. doi: 10.1016/s0960-8966(01)00195-x. Neuromuscul Disord. 2001. PMID: 11404121

3

MERRF syndrome without ragged-red fibers: the need for molecular diagnosis.

Mancuso M, Petrozzi L, Filosto M, Nesti C, Rocchi A, Choub A, Pistolesi S, Massetani R, Fontanini G, Siciliano G. Mancuso M, et al. Among authors: filosto m. Biochem Biophys Res Commun. 2007 Mar 23;354(4):1058-60. doi: 10.1016/j.bbrc.2007.01.099. Epub 2007 Jan 26. Biochem Biophys Res Commun. 2007. PMID: 17275787

4

Mitochondrial DNA-related disorders.

Mancuso M, Filosto M, Choub A, Tentorio M, Broglio L, Padovani A, Siciliano G. Mancuso M, et al. Among authors: filosto m. Biosci Rep. 2007 Jun;27(1-3):31-7. doi: 10.1007/s10540-007-9035-2. Biosci Rep. 2007. PMID: 17484046 Review.

5

Neuropathology of mitochondrial diseases.

Filosto M, Tomelleri G, Tonin P, Scarpelli M, Vattemi G, Rizzuto N, Padovani A, Simonati A. Filosto M, et al. Biosci Rep. 2007 Jun;27(1-3):23-30. doi: 10.1007/s10540-007-9034-3. Biosci Rep. 2007. PMID: 17541738 Review.

6

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: filosto m. 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

7

A high-dose bortezomib neuropathy with sensory ataxia and myelin involvement.

Filosto M, Rossi G, Pelizzari AM, Buzio S, Tentorio M, Broglio L, Mancuso M, Rinaldi M, Scarpelli M, Padovani A. Filosto M, et al. J Neurol Sci. 2007 Dec 15;263(1-2):40-3. doi: 10.1016/j.jns.2007.05.023. Epub 2007 Jul 5. J Neurol Sci. 2007. PMID: 17612569

8

Disulfiram neuropathy: two cases of distal axonopathy.

Filosto M, Tentorio M, Broglio L, Buzio S, Lazzarini C, Pasolini MP, Cotelli MS, Scarpelli M, Mancuso M, Choub A, Padovani A. Filosto M, et al. Clin Toxicol (Phila). 2008 Apr;46(4):314-6. doi: 10.1080/15563650701636390. Clin Toxicol (Phila). 2008. PMID: 18363127

9

Mitochondrial DNA haplogroups do not influence the Huntington's disease phenotype.

Mancuso M, Kiferle L, Petrozzi L, Nesti C, Rocchi A, Ceravolo R, Orsucci D, Maluccio MR, Bonuccelli U, Filosto M, Siciliano G, Murri L. Mancuso M, et al. Among authors: filosto m. Neurosci Lett. 2008 Oct 17;444(1):83-6. doi: 10.1016/j.neulet.2008.08.013. Epub 2008 Aug 8. Neurosci Lett. 2008. PMID: 18706972

10

Idiopathic hypocomplementemic urticarial vasculitis-linked neuropathy.

Filosto M, Cavallaro T, Pasolini G, Broglio L, Tentorio M, Cotelli M, Ferrari S, Padovani A. Filosto M, et al. J Neurol Sci. 2009 Sep 15;284(1-2):179-81. doi: 10.1016/j.jns.2009.03.027. Epub 2009 Apr 16. J Neurol Sci. 2009. PMID: 19375087

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