Massa R - Search Results

1

Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues.

Rinaldi F, Terracciano C, Pisani V, Massa R, Loro E, Vergani L, Di Girolamo S, Angelini C, Gourdon G, Novelli G, Botta A. Rinaldi F, et al. Among authors: massa r. Neurobiol Dis. 2012 Jan;45(1):264-71. doi: 10.1016/j.nbd.2011.08.010. Epub 2011 Aug 18. Neurobiol Dis. 2012. PMID: 21872659 Free article.

2

The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' muscles.

Massa R, Panico MB, Caldarola S, Fusco FR, Sabatelli P, Terracciano C, Botta A, Novelli G, Bernardi G, Loreni F. Massa R, et al. Neuropathol Appl Neurobiol. 2010 Jun;36(4):275-84. doi: 10.1111/j.1365-2990.2010.01068.x. Epub 2009 Nov 20. Neuropathol Appl Neurobiol. 2010. PMID: 20102514

3

Preferential central nucleation of type 2 myofibers is an invariable feature of myotonic dystrophy type 2.

Pisani V, Panico MB, Terracciano C, Bonifazi E, Meola G, Novelli G, Bernardi G, Angelini C, Massa R. Pisani V, et al. Among authors: massa r. Muscle Nerve. 2008 Nov;38(5):1405-1411. doi: 10.1002/mus.21122. Muscle Nerve. 2008. PMID: 18816606

4

Aquaporin 4 expression in human skeletal muscle fiber types.

Vizzaccaro E, Terracciano C, Rastelli E, Massa R. Vizzaccaro E, et al. Among authors: massa r. Muscle Nerve. 2018 May;57(5):856-858. doi: 10.1002/mus.26024. Epub 2017 Dec 20. Muscle Nerve. 2018. PMID: 29193153

5

Expanded [CCTG]n repetitions are not associated with abnormal methylation at the CNBP locus in myotonic dystrophy type 2 (DM2) patients.

Santoro M, Fontana L, Maiorca F, Centofanti F, Massa R, Silvestri G, Novelli G, Botta A. Santoro M, et al. Among authors: massa r. Biochim Biophys Acta Mol Basis Dis. 2018 Mar;1864(3):917-924. doi: 10.1016/j.bbadis.2017.12.037. Epub 2017 Dec 29. Biochim Biophys Acta Mol Basis Dis. 2018. PMID: 29291944 Free article.

6

Validation of the Nine Hole Peg Test as a measure of dexterity in myotonic dystrophy type 1.

Cutellè C, Rastelli E, Gibellini M, Greco G, Frezza E, Botta A, Terracciano C, Massa R. Cutellè C, et al. Among authors: massa r. Neuromuscul Disord. 2018 Nov;28(11):947-951. doi: 10.1016/j.nmd.2018.08.011. Epub 2018 Aug 31. Neuromuscul Disord. 2018. PMID: 30270126

7

Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2).

Botta A, Caldarola S, Vallo L, Bonifazi E, Fruci D, Gullotta F, Massa R, Novelli G, Loreni F. Botta A, et al. Among authors: massa r. Biochim Biophys Acta. 2006 Mar;1762(3):329-34. doi: 10.1016/j.bbadis.2005.11.004. Epub 2005 Dec 6. Biochim Biophys Acta. 2006. PMID: 16376058 Free article.

8

Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients.

Salehi LB, Bonifazi E, Stasio ED, Gennarelli M, Botta A, Vallo L, Iraci R, Massa R, Antonini G, Angelini C, Novelli G. Salehi LB, et al. Among authors: massa r. Genet Test. 2007 Spring;11(1):84-90. doi: 10.1089/gte.2006.0511. Genet Test. 2007. PMID: 17394397

9

Early subclinical cochlear dysfunction in myotonic dystrophy type 1.

Pisani V, Tirabasso A, Mazzone S, Terracciano C, Botta A, Novelli G, Bernardi G, Massa R, Di Girolamo S. Pisani V, et al. Among authors: massa r. Eur J Neurol. 2011 Dec;18(12):1412-6. doi: 10.1111/j.1468-1331.2011.03470.x. Epub 2011 Jul 21. Eur J Neurol. 2011. PMID: 21777352

10

An Age-Standardized Prevalence Estimate and a Sex and Age Distribution of Myotonic Dystrophy Types 1 and 2 in the Rome Province, Italy.

Vanacore N, Rastelli E, Antonini G, Bianchi ML, Botta A, Bucci E, Casali C, Costanzi-Porrini S, Giacanelli M, Gibellini M, Modoni A, Novelli G, Pennisi EM, Petrucci A, Piantadosi C, Silvestri G, Terracciano C, Massa R. Vanacore N, et al. Among authors: massa r. Neuroepidemiology. 2016;46(3):191-7. doi: 10.1159/000444018. Epub 2016 Feb 17. Neuroepidemiology. 2016. PMID: 26882032

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