Mancinelli E - Search Results

1

Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2.

Vihola A, Bassez G, Meola G, Zhang S, Haapasalo H, Paetau A, Mancinelli E, Rouche A, Hogrel JY, Laforêt P, Maisonobe T, Pellissier JF, Krahe R, Eymard B, Udd B. Vihola A, et al. Among authors: mancinelli e. Neurology. 2003 Jun 10;60(11):1854-7. doi: 10.1212/01.wnl.0000065898.61358.09. Neurology. 2003. PMID: 12796551 Free article.

2

Proximal myotonic dystrophy mimicking progressive muscular atrophy.

Rotondo G, Sansone V, Cardani R, Mancinelli E, Krahe R, Stangalini D, Meola G. Rotondo G, et al. Among authors: mancinelli e. Eur J Neurol. 2005 Feb;12(2):160-1. doi: 10.1111/j.1468-1331.2004.01032.x. Eur J Neurol. 2005. PMID: 15679706 No abstract available.

3

Biomolecular identification of (CCTG)n mutation in myotonic dystrophy type 2 (DM2) by FISH on muscle biopsy.

Cardani R, Mancinelli E, Sansone V, Rotondo G, Meola G. Cardani R, et al. Among authors: mancinelli e. Eur J Histochem. 2004 Oct-Dec;48(4):437-42. doi: 10.4081/918. Eur J Histochem. 2004. PMID: 15718211

4

Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2.

Cardani R, Mancinelli E, Rotondo G, Sansone V, Meola G. Cardani R, et al. Among authors: mancinelli e. Eur J Histochem. 2006 Jul-Sep;50(3):177-82. Eur J Histochem. 2006. PMID: 16920640 Free article.

5

Ribonuclear inclusions as biomarker of myotonic dystrophy type 2, even in improperly frozen or defrozen skeletal muscle biopsies.

Cardani R, Mancinelli E, Giagnacovo M, Sansone V, Meola G. Cardani R, et al. Among authors: mancinelli e. Eur J Histochem. 2009 Apr-Jun;53(2):e13. doi: 10.4081/ejh.2009.e13. Eur J Histochem. 2009. PMID: 19683984 Free PMC article.

6

Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2.

Botta A, Vallo L, Rinaldi F, Bonifazi E, Amati F, Biancolella M, Gambardella S, Mancinelli E, Angelini C, Meola G, Novelli G. Botta A, et al. Among authors: mancinelli e. Gene Expr. 2007;13(6):339-51. doi: 10.3727/000000006781510705. Gene Expr. 2007. PMID: 17708420 Free PMC article.

7

A putative role of ribonuclear inclusions and MBNL1 in the impairment of gallbladder smooth muscle contractility with cholelithiasis in myotonic dystrophy type 1.

Cardani R, Mancinelli E, Saino G, Bonavina L, Meola G. Cardani R, et al. Among authors: mancinelli e. Neuromuscul Disord. 2008 Aug;18(8):641-5. doi: 10.1016/j.nmd.2008.06.366. Epub 2008 Jul 23. Neuromuscul Disord. 2008. PMID: 18653337

8

[No title available]

[No authors listed] [No authors listed] PMID: 30256867

9

Ribonuclear inclusions and MBNL1 nuclear sequestration do not affect myoblast differentiation but alter gene splicing in myotonic dystrophy type 2.

Cardani R, Baldassa S, Botta A, Rinaldi F, Novelli G, Mancinelli E, Meola G. Cardani R, et al. Among authors: mancinelli e. Neuromuscul Disord. 2009 May;19(5):335-43. doi: 10.1016/j.nmd.2009.03.002. Epub 2009 Apr 3. Neuromuscul Disord. 2009. PMID: 19345584

10

Proteome profile in Myotonic Dystrophy type 2 myotubes reveals dysfunction in protein processing and mitochondrial pathways.

Rusconi F, Mancinelli E, Colombo G, Cardani R, Da Riva L, Bongarzone I, Meola G, Zippel R. Rusconi F, et al. Among authors: mancinelli e. Neurobiol Dis. 2010 May;38(2):273-80. doi: 10.1016/j.nbd.2010.01.017. Epub 2010 Feb 4. Neurobiol Dis. 2010. PMID: 20138216

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