Filosto M - Search Results

1

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

2

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. Among authors: filosto m. 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

3

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: filosto m. 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

4

Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene.

Mancuso M, Filosto M, Bonilla E, Hirano M, Shanske S, Vu TH, DiMauro S. Mancuso M, et al. Among authors: filosto m. Arch Neurol. 2003 Jul;60(7):1007-9. doi: 10.1001/archneur.60.7.1007. Arch Neurol. 2003. PMID: 12873860

5

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

6

P301L Tau mutation and non-Alzheimer dementias in Italy.

Mancuso M, Leone M, Filosto M, Tognoni G, Siciliano G, Nichelli P, Murri L. Mancuso M, et al. Among authors: filosto m. Acta Neurol Scand. 2003 Nov;108(5):379-80. doi: 10.1034/j.1600-0404.2003.00188.x. Acta Neurol Scand. 2003. PMID: 14616311 No abstract available.

7

Hepato-cerebral syndrome: genetic and pathological studies in an infant with a dGK mutation.

Filosto M, Mancuso M, Tomelleri G, Rizzuto N, Dalla Bernardina B, DiMauro S, Simonati A. Filosto M, et al. Acta Neuropathol. 2004 Aug;108(2):168-71. doi: 10.1007/s00401-004-0872-9. Epub 2004 May 19. Acta Neuropathol. 2004. PMID: 15150663

8

A non-syndromic hearing loss caused by very low levels of the mtDNA A3243G mutation.

Mancuso M, Filosto M, Forli F, Rocchi A, Berrettini S, Siciliano G, Murri L. Mancuso M, et al. Among authors: filosto m. Acta Neurol Scand. 2004 Jul;110(1):72-4. doi: 10.1111/j.1600-0404.2004.00254.x. Acta Neurol Scand. 2004. PMID: 15180810

9

A novel mitochondrial tRNAPhe mutation causes MERRF syndrome.

Mancuso M, Filosto M, Mootha VK, Rocchi A, Pistolesi S, Murri L, DiMauro S, Siciliano G. Mancuso M, et al. Among authors: filosto m. Neurology. 2004 Jun 8;62(11):2119-21. doi: 10.1212/01.wnl.0000127608.48406.f1. Neurology. 2004. PMID: 15184630

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

247 results

Search Page