Rinaldi F - Search Results

1

Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells.

Loro E, Rinaldi F, Malena A, Masiero E, Novelli G, Angelini C, Romeo V, Sandri M, Botta A, Vergani L. Loro E, et al. Among authors: rinaldi f. Cell Death Differ. 2010 Aug;17(8):1315-24. doi: 10.1038/cdd.2010.33. Epub 2010 Apr 30. Cell Death Differ. 2010. PMID: 20431600

2

The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients.

Botta A, Rinaldi F, Catalli C, Vergani L, Bonifazi E, Romeo V, Loro E, Viola A, Angelini C, Novelli G. Botta A, et al. Among authors: rinaldi f. J Med Genet. 2008 Oct;45(10):639-46. doi: 10.1136/jmg.2008.058909. Epub 2008 Jul 8. J Med Genet. 2008. PMID: 18611984

3

Overexpression of microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patients.

Gambardella S, Rinaldi F, Lepore SM, Viola A, Loro E, Angelini C, Vergani L, Novelli G, Botta A. Gambardella S, et al. Among authors: rinaldi f. J Transl Med. 2010 May 20;8:48. doi: 10.1186/1479-5876-8-48. J Transl Med. 2010. PMID: 20487562 Free PMC article.

4

Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients.

Rinaldi F, Botta A, Vallo L, Contino G, Morgante A, Iraci R, Catalli C, Silvestri G, Ventriglia VM, Politano L, Novelli G. Rinaldi F, et al. Acta Myol. 2008 Dec;27(3):82-9. Acta Myol. 2008. PMID: 19472917 Free PMC article.

5

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. 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.

6

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: rinaldi f. 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

7

Validation of sensitivity and specificity of tetraplet-primed PCR (TP-PCR) in the molecular diagnosis of myotonic dystrophy type 2 (DM2).

Catalli C, Morgante A, Iraci R, Rinaldi F, Botta A, Novelli G. Catalli C, et al. Among authors: rinaldi f. J Mol Diagn. 2010 Sep;12(5):601-6. doi: 10.2353/jmoldx.2010.090239. Epub 2010 Jul 8. J Mol Diagn. 2010. PMID: 20616365 Free PMC article.

8

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: rinaldi f. Gene Expr. 2007;13(6):339-51. doi: 10.3727/000000006781510705. Gene Expr. 2007. PMID: 17708420 Free PMC article.

9

Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2.

Cardani R, Giagnacovo M, Botta A, Rinaldi F, Morgante A, Udd B, Raheem O, Penttilä S, Suominen T, Renna LV, Sansone V, Bugiardini E, Novelli G, Meola G. Cardani R, et al. Among authors: rinaldi f. J Neurol. 2012 Oct;259(10):2090-9. doi: 10.1007/s00415-012-6462-1. Epub 2012 Mar 10. J Neurol. 2012. PMID: 22407275

10

Novel mutations of TCOF1 gene in European patients with Treacher Collins syndrome.

Conte C, D'Apice MR, Rinaldi F, Gambardella S, Sangiuolo F, Novelli G. Conte C, et al. Among authors: rinaldi f. BMC Med Genet. 2011 Sep 27;12:125. doi: 10.1186/1471-2350-12-125. BMC Med Genet. 2011. PMID: 21951868 Free PMC article.

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