Broccolini A - Search Results

1

Mesoangioblasts of inclusion-body myositis: a twofold tool to study pathogenic mechanisms and enhance defective muscle regeneration.

Morosetti R, Gliubizzi C, Broccolini A, Sancricca C, Mirabella M. Morosetti R, et al. Among authors: broccolini a. Acta Myol. 2011 Jun;30(1):24-8. Acta Myol. 2011. PMID: 21842589 Free PMC article. Review.

2

The drastic reduction of SMN protein in SMA I spinal cord motor neurons is not due to inefficient transcription.

Mirabella M, Servidei S, Broccolini A, Gandolfi N, Ricci E, Neri G, Tonali P, Brahe C. Mirabella M, et al. Among authors: broccolini a. Neurogenetics. 1999 Apr;2(2):97-100. doi: 10.1007/s100480050059. Neurogenetics. 1999. PMID: 10369885

3

Coenzyme Q10 reverses pathological phenotype and reduces apoptosis in familial CoQ10 deficiency.

Di Giovanni S, Mirabella M, Spinazzola A, Crociani P, Silvestri G, Broccolini A, Tonali P, Di Mauro S, Servidei S. Di Giovanni S, et al. Among authors: broccolini a. Neurology. 2001 Aug 14;57(3):515-8. doi: 10.1212/wnl.57.3.515. Neurology. 2001. PMID: 11502923

4

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. Neurology. 2002 Dec 10;59(11):1808-9. doi: 10.1212/01.wnl.0000031808.04545.e0. Neurology. 2002. PMID: 12473780 No abstract available.

5

Pathogenic role of mtDNA duplications in mitochondrial diseases associated with mtDNA deletions.

Odoardi F, Rana M, Broccolini A, Mirabella M, Modoni A, D'Amico A, Papacci M, Tonali P, Servidei S, Silvestri G. Odoardi F, et al. Among authors: broccolini a. Am J Med Genet A. 2003 Apr 30;118A(3):247-54. doi: 10.1002/ajmg.a.20006. Am J Med Genet A. 2003. PMID: 12673655

6

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. Hum Mutat. 2004 Jun;23(6):632. doi: 10.1002/humu.9252. Hum Mutat. 2004. PMID: 15146476

7

Insulin-like growth factor I in inclusion-body myositis and human muscle cultures.

Broccolini A, Ricci E, Pescatori M, Papacci M, Gliubizzi C, D'Amico A, Servidei S, Tonali P, Mirabella M. Broccolini A, et al. J Neuropathol Exp Neurol. 2004 Jun;63(6):650-9. doi: 10.1093/jnen/63.6.650. J Neuropathol Exp Neurol. 2004. PMID: 15217093

8

alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy.

Broccolini A, Gliubizzi C, Pavoni E, Gidaro T, Morosetti R, Sciandra F, Giardina B, Tonali P, Ricci E, Brancaccio A, Mirabella M. Broccolini A, et al. Neuromuscul Disord. 2005 Feb;15(2):177-84. doi: 10.1016/j.nmd.2004.10.001. Epub 2004 Dec 10. Neuromuscul Disord. 2005. PMID: 15694140

9

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. 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.

10

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: broccolini a. Neurology. 2006 Mar 14;66(5):755-8. doi: 10.1212/01.wnl.0000200956.76449.3f. Neurology. 2006. PMID: 16534119

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