Fanin M - Search Results

1

Functional changes in Becker muscular dystrophy: implications for clinical trials in dystrophinopathies.

Bello L, Campadello P, Barp A, Fanin M, Semplicini C, Sorarù G, Caumo L, Calore C, Angelini C, Pegoraro E. Bello L, et al. Among authors: fanin m. Sci Rep. 2016 Sep 1;6:32439. doi: 10.1038/srep32439. Sci Rep. 2016. PMID: 27582364 Free PMC article.

2

TGFBR2 but not SPP1 genotype modulates osteopontin expression in Duchenne muscular dystrophy muscle.

Piva L, Gavassini BF, Bello L, Fanin M, Soraru G, Barp A, Ermani M, Angelini C, Hoffman EP, Pegoraro E. Piva L, et al. Among authors: fanin m. J Pathol. 2012 Oct;228(2):251-9. doi: 10.1002/path.4026. Epub 2012 Aug 28. J Pathol. 2012. PMID: 22431140 Free PMC article.

3

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

4

Progress in Enzyme Replacement Therapy in Glycogen Storage Disease Type II.

Angelini C, Semplicini C, Tonin P, Filosto M, Pegoraro E, Sorarù G, Fanin M. Angelini C, et al. Among authors: fanin m. Ther Adv Neurol Disord. 2009 May;2(3):143-53. doi: 10.1177/1756285609103324. Ther Adv Neurol Disord. 2009. PMID: 21179524 Free PMC article.

5

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.

6

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.

7

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.

8

Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcript.

Todeschini A, Gualandi F, Trabanelli C, Armaroli A, Ravani A, Fanin M, Rota S, Bello L, Ferlini A, Pegoraro E, Padovani A, Filosto M. Todeschini A, et al. Among authors: fanin m. Neuromuscul Disord. 2016 Oct;26(10):662-665. doi: 10.1016/j.nmd.2016.08.007. Epub 2016 Aug 16. Neuromuscul Disord. 2016. PMID: 27616544

9

Enormous dystrophin in a patient with Becker muscular dystrophy.

Angelini C, Beggs AH, Hoffman EP, Fanin M, Kunkel LM. Angelini C, et al. Among authors: fanin m. Neurology. 1990 May;40(5):808-12. doi: 10.1212/wnl.40.5.808. Neurology. 1990. PMID: 2158637

10

Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: characterization of sub-clinical phenotypes.

Angelini C, Fanin M, Pegoraro E, Freda MP, Cadaldini M, Martinello F. Angelini C, et al. Among authors: fanin m. Neuromuscul Disord. 1994 Jul;4(4):349-58. doi: 10.1016/0960-8966(94)90071-x. Neuromuscul Disord. 1994. PMID: 7981592

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