Cacurri S[au] - Search Results

Year	Number of Results
1994	2
1995	1
1996	1
1998	1
1999	2
2024	0

1

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: cacurri s. 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.

2

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. Hum Genet. 1994 Oct;94(4):367-74. doi: 10.1007/BF00201595. Hum Genet. 1994. PMID: 7927331

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: cacurri s. 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: cacurri s. Neuromuscul Disord. 1999 May;9(3):190-8. doi: 10.1016/s0960-8966(98)00116-3. Neuromuscul Disord. 1999. PMID: 10382915

5

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: cacurri s. Eur J Hum Genet. 1995;3(3):155-67. doi: 10.1159/000472291. Eur J Hum Genet. 1995. PMID: 7583041

6

4q35 molecular probes for the diagnosis and genetic counseling of facioscapulohumeral muscular dystrophy.

Deidda GC, Cacurri S, La Cesa I, Scoppetta C, Felicetti L. Deidda GC, et al. Among authors: cacurri s. Ann Neurol. 1994 Jul;36(1):117-8. doi: 10.1002/ana.410360128. Ann Neurol. 1994. PMID: 8024254 No abstract available.

7

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. Am J Hum Genet. 1998 Jul;63(1):181-90. doi: 10.1086/301906. Am J Hum Genet. 1998. PMID: 9634507 Free PMC article.

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