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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 3
2003 3
2005 2
2006 4
2007 2
2008 3
2009 5
2010 5
2011 4
2012 5
2013 4
2014 5
2015 9
2016 7
2017 1
2018 3
2024 0

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57 results

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Fanin M, Nigro V, Angelini C. Fanin M, et al. Muscle Nerve. 2016 Jan;53(1):157-8. doi: 10.1002/mus.24898. Epub 2015 Nov 26. Muscle Nerve. 2016. PMID: 26353085 No abstract available.
Autophagy dysregulation in Danon disease.
Nascimbeni AC, Fanin M, Angelini C, Sandri M. Nascimbeni AC, et al. Among authors: fanin m. Cell Death Dis. 2017 Jan 19;8(1):e2565. doi: 10.1038/cddis.2016.475. Cell Death Dis. 2017. PMID: 28102838 Free PMC article.
Ultrastructural changes in LGMD1F.
Cenacchi G, Peterle E, Fanin M, Papa V, Salaroli R, Angelini C. Cenacchi G, et al. Among authors: fanin m. Neuropathology. 2013 Jun;33(3):276-80. doi: 10.1111/neup.12003. Epub 2012 Dec 21. Neuropathology. 2013. PMID: 23279333
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.
Phenotype modulators in myophosphorylase deficiency.
Martinuzzi A, Sartori E, Fanin M, Nascimbeni A, Valente L, Angelini C, Siciliano G, Mongini T, Tonin P, Tomelleri G, Toscano A, Merlini L, Bindoff LA, Bertelli S. Martinuzzi A, et al. Among authors: fanin m. Ann Neurol. 2003 Apr;53(4):497-502. doi: 10.1002/ana.10499. Ann Neurol. 2003. PMID: 12666117
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. Neuropathol Appl Neurobiol. 2015 Apr;41(3):385-90. doi: 10.1111/nan.12171. Neuropathol Appl Neurobiol. 2015. PMID: 25041762 No abstract available.
57 results