Nascimbeni AC - Search Results

1

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

2

Molecular and muscle pathology in a series of caveolinopathy patients.

Fulizio L, Nascimbeni AC, Fanin M, Piluso G, Politano L, Nigro V, Angelini C. Fulizio L, et al. Among authors: nascimbeni ac. Hum Mutat. 2005 Jan;25(1):82-9. doi: 10.1002/humu.20119. Hum Mutat. 2005. PMID: 15580566

3

The frequency of limb girdle muscular dystrophy 2A in northeastern Italy.

Fanin M, Nascimbeni AC, Fulizio L, Angelini C. Fanin M, et al. Among authors: nascimbeni ac. Neuromuscul Disord. 2005 Mar;15(3):218-24. doi: 10.1016/j.nmd.2004.11.003. Epub 2005 Jan 28. Neuromuscul Disord. 2005. PMID: 15725583

4

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

5

Molecular pathology and enzyme processing in various phenotypes of acid maltase deficiency.

Nascimbeni AC, Fanin M, Tasca E, Angelini C. Nascimbeni AC, et al. Neurology. 2008 Feb 19;70(8):617-26. doi: 10.1212/01.wnl.0000299892.81127.8e. Neurology. 2008. PMID: 18285536

6

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.

7

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.

8

Gender difference in limb-girdle muscular dystrophy: a muscle fiber morphometric study in 101 patients.

Fanin M, Nascimbeni AC, Angelini C. Fanin M, et al. Among authors: nascimbeni ac. Clin Neuropathol. 2014 May-Jun;33(3):179-85. doi: 10.5414/NP300728. Clin Neuropathol. 2014. PMID: 24618072

9

Incomplete penetrance in limb-girdle muscular dystrophy type 1F.

Fanin M, Peterle E, Fritegotto C, Nascimbeni AC, Tasca E, Torella A, Nigro V, Angelini C. Fanin M, et al. Among authors: nascimbeni ac. Muscle Nerve. 2015 Aug;52(2):305-6. doi: 10.1002/mus.24539. Epub 2015 Jun 7. Muscle Nerve. 2015. PMID: 25487718 No abstract available.

10

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.

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