Felicetti L - Search Results

1

Changes in motor cortex excitability in facioscapulohumeral muscular dystrophy.

Di Lazzaro V, Oliviero A, Tonali PA, Felicetti L, De Marco MB, Saturno E, Pilato F, Pescatori M, Dileone M, Pasqualetti P, Ricci E. Di Lazzaro V, et al. Among authors: felicetti l. Neuromuscul Disord. 2004 Jan;14(1):39-45. doi: 10.1016/j.nmd.2003.08.002. Neuromuscul Disord. 2004. PMID: 14659411

2

The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure.

Rossi M, Ricci E, Colantoni L, Galluzzi G, Frusciante R, Tonali PA, Felicetti L. Rossi M, et al. Among authors: felicetti l. BMC Med Genet. 2007 Mar 2;8:8. doi: 10.1186/1471-2350-8-8. BMC Med Genet. 2007. PMID: 17335567 Free PMC article.

3

Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype.

Ricci E, Galluzzi G, Deidda G, Cacurri S, Colantoni L, Merico B, Piazzo N, Servidei S, Vigneti E, Pasceri V, Silvestri G, Mirabella M, Mangiola F, Tonali P, Felicetti L. Ricci E, et al. Among authors: felicetti l. Ann Neurol. 1999 Jun;45(6):751-7. doi: 10.1002/1531-8249(199906)45:6<751::aid-ana9>3.0.co;2-m. Ann Neurol. 1999. PMID: 10360767

4

Molecular analysis of 4q35 rearrangements in fascioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease.

Galluzzi G, Deidda G, Cacurri S, Colantoni L, Piazzo N, Vigneti E, Ricci E, Servidei S, Merico B, Pachì A, Brambati B, Mangiola F, Tonali P, Felicetti L. Galluzzi G, et al. Among authors: felicetti l. Neuromuscul Disord. 1999 May;9(3):190-8. doi: 10.1016/s0960-8966(98)00116-3. Neuromuscul Disord. 1999. PMID: 10382915

5

Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophy.

Cacurri S, Piazzo N, Deidda G, Vigneti E, Galluzzi G, Colantoni L, Merico B, Ricci E, Felicetti L. Cacurri S, et al. Among authors: felicetti l. Am J Hum Genet. 1998 Jul;63(1):181-90. doi: 10.1086/301906. Am J Hum Genet. 1998. PMID: 9634507 Free PMC article.

6

Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy.

van Overveld PG, Enthoven L, Ricci E, Rossi M, Felicetti L, Jeanpierre M, Winokur ST, Frants RR, Padberg GW, van der Maarel SM. van Overveld PG, et al. Among authors: felicetti l. Ann Neurol. 2005 Oct;58(4):569-76. doi: 10.1002/ana.20625. Ann Neurol. 2005. PMID: 16178028

7

Pulse field gel electrophoresis for the detection of facioscapulohumeral muscular dystrophy gene rearrangements.

Felicetti L, Galluzzi G. Felicetti L, et al. Methods Mol Biol. 2003;217:153-64. doi: 10.1385/1-59259-330-5:153. Methods Mol Biol. 2003. PMID: 12491930 No abstract available.

8

Physical mapping evidence for a duplicated region on chromosome 10qter showing high homology with the facioscapulohumeral muscular dystrophy locus on chromosome 4qter.

Deidda G, Cacurri S, Grisanti P, Vigneti E, Piazzo N, Felicetti L. Deidda G, et al. Among authors: felicetti l. Eur J Hum Genet. 1995;3(3):155-67. doi: 10.1159/000472291. Eur J Hum Genet. 1995. PMID: 7583041

9

Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD).

Cacurri S, Deidda G, Piazzo N, Novelletto A, La Cesa I, Servidei S, Galluzzi G, Wijmenga C, Frants RR, Felicetti L. Cacurri S, et al. Among authors: felicetti l. Hum Genet. 1994 Oct;94(4):367-74. doi: 10.1007/BF00201595. Hum Genet. 1994. PMID: 7927331

10

Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD).

Deidda G, Cacurri S, Piazzo N, Felicetti L. Deidda G, et al. Among authors: felicetti l. J Med Genet. 1996 May;33(5):361-5. doi: 10.1136/jmg.33.5.361. J Med Genet. 1996. PMID: 8733043 Free PMC article.

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