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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):107-11. doi: 10.4081/ejh.2009.107. Eur J Histochem. 2009. PMID: 19683984
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
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.
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
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
RNA/MBNL1-containing foci in myoblast nuclei from patients affected by myotonic dystrophy type 2: an immunocytochemical study.
Perdoni F, Malatesta M, Cardani R, Giagnacovo M, Mancinelli E, Meola G, Pellicciari C. Perdoni F, et al. Among authors: mancinelli e. Eur J Histochem. 2009 Sep 30;53(3):e18. doi: 10.4081/ejh.2009.e18. eCollection 2009 Sep 30. Eur J Histochem. 2009. PMID: 30256871 Free PMC article. Review.
RNA/MBNL1-containing foci in myoblast nuclei from patients affected by myotonic dystrophy type 2: an immunocytochemical study.
Perdoni F, Malatesta M, Cardani R, Giagnacovo M, Mancinelli E, Meola G, Pellicciari C. Perdoni F, et al. Among authors: mancinelli e. Eur J Histochem. 2009 Sep 23;53(3):151-8. doi: 10.4081/ejh.2009.151. Eur J Histochem. 2009. PMID: 19864209
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
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion.
Lucchiari S, Pagliarani S, Corti S, Mancinelli E, Servida M, Fruguglietti E, Sansone V, Moggio M, Bresolin N, Comi GP, Meola G. Lucchiari S, et al. Among authors: mancinelli e. J Neurol Sci. 2008 Dec 15;275(1-2):159-63. doi: 10.1016/j.jns.2008.08.007. Epub 2008 Sep 18. J Neurol Sci. 2008. PMID: 18804219
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, LaforĂȘt 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
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