Filosto M - Search Results

1

Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis.

Ricci G, Mele F, Govi M, Ruggiero L, Sera F, Vercelli L, Bettio C, Santoro L, Mongini T, Villa L, Moggio M, Filosto M, Scarlato M, Previtali SC, Tripodi SM, Pegoraro E, Telese R, Di Muzio A, Rodolico C, Bucci E, Antonini G, D'Angelo MG, Berardinelli A, Maggi L, Piras R, Maioli MA, Siciliano G, Tomelleri G, Angelini C, Tupler R. Ricci G, et al. Among authors: filosto m. Sci Rep. 2020 Dec 10;10(1):21648. doi: 10.1038/s41598-020-78578-7. Sci Rep. 2020. PMID: 33303865 Free PMC article.

2

T-cell anti-apoptotic mechanisms in inflammatory myopathies.

Vattemi G, Tonin P, Filosto M, Spagnolo M, Rizzuto N, Tomelleri G. Vattemi G, et al. Among authors: filosto m. J Neuroimmunol. 2000 Nov 1;111(1-2):146-51. doi: 10.1016/s0165-5728(00)00381-7. J Neuroimmunol. 2000. PMID: 11063832

3

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

4

Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases.

Filosto M, Tonin P, Vattemi G, Spagnolo M, Rizzuto N, Tomelleri G. Filosto M, et al. Acta Neuropathol. 2002 Mar;103(3):215-20. doi: 10.1007/s004010100455. Epub 2001 Nov 16. Acta Neuropathol. 2002. PMID: 11907800

5

Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mitochondrial diseases.

Filosto M, Tonin P, Vattemi G, Savio C, Rizzuto N, Tomelleri G. Filosto M, et al. Neuropathol Appl Neurobiol. 2003 Feb;29(1):52-9. doi: 10.1046/j.1365-2990.2003.00411.x. Neuropathol Appl Neurobiol. 2003. PMID: 12581340

6

Reversible upper limb muscle weakness with selective loss of thick filaments.

Vattemi G, Tonin P, Filosto M, Savio C, Rizzuto N, Tomelleri G. Vattemi G, et al. Among authors: filosto m. Neurology. 2003 Sep 23;61(6):863-4. doi: 10.1212/wnl.61.6.863. Neurology. 2003. PMID: 14504344 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

Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy.

Vattemi G, Tomelleri G, Filosto M, Savio C, Rizzuto N, Tonin P. Vattemi G, et al. Among authors: filosto m. Neuropathol Appl Neurobiol. 2005 Feb;31(1):45-52. doi: 10.1111/j.1365-2990.2004.00602.x. Neuropathol Appl Neurobiol. 2005. PMID: 15634230

9

McArdle disease: the mutation spectrum of PYGM in a large Italian cohort.

Bruno C, Cassandrini D, Martinuzzi A, Toscano A, Moggio M, Morandi L, Servidei S, Mongini T, Angelini C, Musumeci O, Comi GP, Lamperti C, Filosto M, Zara F, Minetti C. Bruno C, et al. Among authors: filosto m. Hum Mutat. 2006 Jul;27(7):718. doi: 10.1002/humu.9434. Hum Mutat. 2006. PMID: 16786513

10

Mitochondrial dysfunction and Alzheimer's disease: new developments.

Mancuso M, Siciliano G, Filosto M, Murri L. Mancuso M, et al. Among authors: filosto m. J Alzheimers Dis. 2006 Jul;9(2):111-7. doi: 10.3233/jad-2006-9203. J Alzheimers Dis. 2006. PMID: 16873958 Review.

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