Nascimbeni AC - Search Results

1

The clinical course of calpainopathy (LGMD2A) and dysferlinopathy (LGMD2B).

Angelini C, Nardetto L, Borsato C, Padoan R, Fanin M, Nascimbeni AC, Tasca E. Angelini C, et al. Among authors: nascimbeni ac. Neurol Res. 2010 Feb;32(1):41-6. doi: 10.1179/174313209X380847. Neurol Res. 2010. PMID: 20092694

2

Muscle protein analysis in the detection of heterozygotes for recessive limb girdle muscular dystrophy type 2B and 2E.

Fanin M, Nascimbeni AC, Angelini C. Fanin M, et al. Among authors: nascimbeni ac. Neuromuscul Disord. 2006 Nov;16(11):792-9. doi: 10.1016/j.nmd.2006.06.010. Epub 2006 Aug 23. Neuromuscul Disord. 2006. PMID: 16934466

3

How to tackle the diagnosis of limb-girdle muscular dystrophy 2A.

Fanin M, Nascimbeni AC, Tasca E, Angelini C. Fanin M, et al. Among authors: nascimbeni ac. Eur J Hum Genet. 2009 May;17(5):598-603. doi: 10.1038/ejhg.2008.193. Epub 2008 Oct 15. Eur J Hum Genet. 2009. PMID: 18854869 Free PMC article.

4

Sarcolemmal neuronal nitric oxide synthase defect in limb-girdle muscular dystrophy: an adverse modulating factor in the disease course?

Fanin M, Tasca E, Nascimbeni AC, Angelini C. Fanin M, et al. Among authors: nascimbeni ac. J Neuropathol Exp Neurol. 2009 Apr;68(4):383-90. doi: 10.1097/NEN.0b013e31819cd612. J Neuropathol Exp Neurol. 2009. PMID: 19287313

5

Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutations.

Fanin M, Nascimbeni AC, Angelini C. Fanin M, et al. Among authors: nascimbeni ac. J Med Genet. 2007 Jan;44(1):38-43. doi: 10.1136/jmg.2006.044859. Epub 2006 Sep 13. J Med Genet. 2007. PMID: 16971480 Free PMC article.

6

Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2A.

Fanin M, Nardetto L, Nascimbeni AC, Tasca E, Spinazzi M, Padoan R, Angelini C. Fanin M, et al. Among authors: nascimbeni ac. J Med Genet. 2007 Oct;44(10):609-14. doi: 10.1136/jmg.2007.050328. Epub 2007 May 25. J Med Genet. 2007. PMID: 17526799 Free PMC article.

7

Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes.

Fanin M, Nascimbeni AC, Aurino S, Tasca E, Pegoraro E, Nigro V, Angelini C. Fanin M, et al. Among authors: nascimbeni ac. Neurology. 2009 Apr 21;72(16):1432-5. doi: 10.1212/WNL.0b013e3181a1885e. Neurology. 2009. PMID: 19380703

8

Muscle atrophy in Limb Girdle Muscular Dystrophy 2A: a morphometric and molecular study.

Fanin M, Nascimbeni AC, Angelini C. Fanin M, et al. Among authors: nascimbeni ac. Neuropathol Appl Neurobiol. 2013 Dec;39(7):762-71. doi: 10.1111/nan.12034. Neuropathol Appl Neurobiol. 2013. PMID: 23414389 Free article.

9

Muscle fatigue, nNOS and muscle fiber atrophy in limb girdle muscular dystrophy.

Angelini C, Tasca E, Nascimbeni AC, Fanin M. Angelini C, et al. Among authors: nascimbeni ac. Acta Myol. 2014 Dec;33(3):119-26. Acta Myol. 2014. PMID: 25873780 Free PMC article. Review.

10

Loss of calpain-3 autocatalytic activity in LGMD2A patients with normal protein expression.

Fanin M, Nascimbeni AC, Fulizio L, Trevisan CP, Meznaric-Petrusa M, Angelini C. Fanin M, et al. Among authors: nascimbeni ac. Am J Pathol. 2003 Nov;163(5):1929-36. doi: 10.1016/S0002-9440(10)63551-1. Am J Pathol. 2003. PMID: 14578192 Free PMC article.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

57 results

Search Page

Filters