Fanin M - Search Results

1

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

Fanin M, Nascimbeni AC, Fulizio L, Angelini C. Fanin M, et al. 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

2

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. 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.

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: fanin m. Hum Mutat. 2005 Jan;25(1):82-9. doi: 10.1002/humu.20119. Hum Mutat. 2005. PMID: 15580566

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. 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

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

Fanin M, Nascimbeni AC, Tasca E, Angelini C. Fanin M, et al. 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.

6

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. J Neuropathol Exp Neurol. 2009 Apr;68(4):383-90. doi: 10.1097/NEN.0b013e31819cd612. J Neuropathol Exp Neurol. 2009. PMID: 19287313

7

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. 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.

8

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: fanin m. Acta Myol. 2014 Dec;33(3):119-26. Acta Myol. 2014. PMID: 25873780 Free PMC article. Review.

9

Protein and genetic diagnosis of limb girdle muscular dystrophy type 2A: The yield and the pitfalls.

Fanin M, Angelini C. Fanin M, et al. Muscle Nerve. 2015 Aug;52(2):163-73. doi: 10.1002/mus.24682. Epub 2015 May 29. Muscle Nerve. 2015. PMID: 25900067 Review.

10

Progress and challenges in diagnosis of dysferlinopathy.

Fanin M, Angelini C. Fanin M, et al. Muscle Nerve. 2016 Nov;54(5):821-835. doi: 10.1002/mus.25367. Muscle Nerve. 2016. PMID: 27501525 Review.

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

130 results

Search Page

Filters