Tonali PA - Search Results

1

NCAM is hyposialylated in hereditary inclusion body myopathy due to GNE mutations.

Ricci E, Broccolini A, Gidaro T, Morosetti R, Gliubizzi C, Frusciante R, Di Lella GM, Tonali PA, Mirabella M. Ricci E, et al. Among authors: tonali pa. Neurology. 2006 Mar 14;66(5):755-8. doi: 10.1212/01.wnl.0000200956.76449.3f. Neurology. 2006. PMID: 16534119

2

Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle.

Broccolini A, Gidaro T, De Cristofaro R, Morosetti R, Gliubizzi C, Ricci E, Tonali PA, Mirabella M. Broccolini A, et al. Among authors: tonali pa. J Neurochem. 2008 May;105(3):971-81. doi: 10.1111/j.1471-4159.2007.05208.x. Epub 2007 Dec 24. J Neurochem. 2008. PMID: 18182043 Free article.

3

Increased aging in primary muscle cultures of sporadic inclusion-body myositis.

Morosetti R, Broccolini A, Sancricca C, Gliubizzi C, Gidaro T, Tonali PA, Ricci E, Mirabella M. Morosetti R, et al. Among authors: tonali pa. Neurobiol Aging. 2010 Jul;31(7):1205-14. doi: 10.1016/j.neurobiolaging.2008.08.011. Epub 2008 Sep 26. Neurobiol Aging. 2010. PMID: 18823681

4

Novel GNE mutations in Italian families with autosomal recessive hereditary inclusion-body myopathy.

Broccolini A, Ricci E, Cassandrini D, Gliubizzi C, Bruno C, Tonoli E, Silvestri G, Pescatori M, Rodolico C, Sinicropi S, Servidei S, Zara F, Minetti C, Tonali PA, Mirabella M. Broccolini A, et al. Among authors: tonali pa. Hum Mutat. 2004 Jun;23(6):632. doi: 10.1002/humu.9252. Hum Mutat. 2004. PMID: 15146476

5

Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis.

Broccolini A, Gidaro T, Morosetti R, Gliubizzi C, Servidei T, Pescatori M, Tonali PA, Ricci E, Mirabella M. Broccolini A, et al. Among authors: tonali pa. J Neurochem. 2006 Feb;96(3):777-89. doi: 10.1111/j.1471-4159.2005.03584.x. Epub 2006 Jan 9. J Neurochem. 2006. PMID: 16405511 Free article.

6

An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene.

Broccolini A, Pescatori M, D'Amico A, Sabino A, Silvestri G, Ricci E, Servidei S, Tonali PA, Mirabella M. Broccolini A, et al. Among authors: tonali pa. Neurology. 2002 Dec 10;59(11):1808-9. doi: 10.1212/01.wnl.0000031808.04545.e0. Neurology. 2002. PMID: 12473780 No abstract available.

7

Chronic autoimmune autonomic neuropathy responsive to immunosuppressive therapy.

Modoni A, Mirabella M, Madia F, Sanna T, Lanza G, Tonali PA, Silvestri G. Modoni A, et al. Among authors: tonali pa. Neurology. 2007 Jan 9;68(2):161-2. doi: 10.1212/01.wnl.0000251194.82212.75. Neurology. 2007. PMID: 17210903 No abstract available.

8

Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies.

Servidei S, Zeviani M, Manfredi G, Ricci E, Silvestri G, Bertini E, Gellera C, Di Mauro S, Di Donato S, Tonali P. Servidei S, et al. Neurology. 1991 Jul;41(7):1053-9. doi: 10.1212/wnl.41.7.1053. Neurology. 1991. PMID: 2067633

9

Relapsing-remitting autoimmune agrypnia.

Batocchi AP, Della Marca G, Mirabella M, Caggiula M, Frisullo G, Mennuni GF, Tonali PA. Batocchi AP, et al. Among authors: tonali pa. Ann Neurol. 2001 Nov;50(5):668-71. doi: 10.1002/ana.1261. Ann Neurol. 2001. PMID: 11706975

10

Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression.

Pescatori M, Broccolini A, Minetti C, Bertini E, Bruno C, D'amico A, Bernardini C, Mirabella M, Silvestri G, Giglio V, Modoni A, Pedemonte M, Tasca G, Galluzzi G, Mercuri E, Tonali PA, Ricci E. Pescatori M, et al. Among authors: tonali pa. FASEB J. 2007 Apr;21(4):1210-26. doi: 10.1096/fj.06-7285com. Epub 2007 Jan 30. FASEB J. 2007. PMID: 17264171

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