Nascimbeni AC - Search Results

1

Morphological changes in late onset acid Maltase deficient patients with splicing gene mutation.

Angelini C, Cenacchi G, Nascimbeni AC, Fulizio L. Angelini C, et al. Among authors: nascimbeni ac. Acta Myol. 2003 Dec;22(3):90-6. Acta Myol. 2003. PMID: 15088498

2

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

3

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

4

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

5

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

6

Transcriptional and translational effects of intronic CAPN3 gene mutations.

Nascimbeni AC, Fanin M, Tasca E, Angelini C. Nascimbeni AC, et al. Hum Mutat. 2010 Sep;31(9):E1658-69. doi: 10.1002/humu.21320. Hum Mutat. 2010. PMID: 20635405 Free PMC article.

7

Impaired autophagy contributes to muscle atrophy in glycogen storage disease type II patients.

Nascimbeni AC, Fanin M, Masiero E, Angelini C, Sandri M. Nascimbeni AC, et al. Autophagy. 2012 Nov;8(11):1697-700. doi: 10.4161/auto.21691. Epub 2012 Aug 31. Autophagy. 2012. PMID: 22940840 Free PMC article.

8

Familial polyglucosan body myopathy with unusual phenotype.

Fanin M, Nascimbeni AC, Savarese M, Papa V, Cenacchi G, Nigro V, Angelini C. Fanin M, et al. Among authors: nascimbeni ac. Neuropathol Appl Neurobiol. 2015 Apr;41(3):385-90. doi: 10.1111/nan.12171. Neuropathol Appl Neurobiol. 2015. PMID: 25041762 No abstract available.

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

Effects of short-to-long term enzyme replacement therapy (ERT) on skeletal muscle tissue in late onset Pompe disease (LOPD).

Ripolone M, Violano R, Ronchi D, Mondello S, Nascimbeni A, Colombo I, Fagiolari G, Bordoni A, Fortunato F, Lucchini V, Saredi S, Filosto M, Musumeci O, Tonin P, Mongini T, Previtali S, Morandi L, Angelini C, Mora M, Sandri M, Sciacco M, Toscano A, Comi GP, Moggio M. Ripolone M, et al. Neuropathol Appl Neurobiol. 2018 Aug;44(5):449-462. doi: 10.1111/nan.12414. Epub 2017 Jul 4. Neuropathol Appl Neurobiol. 2018. PMID: 28574618 Free article.

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