Spadaro M - Search Results

1

Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions.

Frontali M, Sabbadini G, Novelletto A, Jodice C, Naso F, Spadaro M, Giunti P, Jacopini AG, Veneziano L, Mantuano E, Malaspina P, Ulizzi L, Brice A, Durr A, Terrenato L. Frontali M, et al. Among authors: spadaro m. Ann Hum Genet. 1996 Sep;60(5):423-35. doi: 10.1111/j.1469-1809.1996.tb00440.x. Ann Hum Genet. 1996. PMID: 8912795 Free article.

2

Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I.

Jodice C, Malaspina P, Persichetti F, Novelletto A, Spadaro M, Giunti P, Morocutti C, Terrenato L, Harding AE, Frontali M. Jodice C, et al. Among authors: spadaro m. Am J Hum Genet. 1994 Jun;54(6):959-65. Am J Hum Genet. 1994. PMID: 8198139 Free PMC article.

3

The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci.

Jodice C, Frontali M, Persichetti F, Novelletto A, Pandolfo M, Spadaro M, Giunti P, Schinaia G, Lulli P, Malaspina P, et al. Jodice C, et al. Among authors: spadaro m. Hum Mol Genet. 1993 Sep;2(9):1383-7. doi: 10.1093/hmg/2.9.1383. Hum Mol Genet. 1993. PMID: 8242061

4

Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p.

Jodice C, Mantuano E, Veneziano L, Trettel F, Sabbadini G, Calandriello L, Francia A, Spadaro M, Pierelli F, Salvi F, Ophoff RA, Frants RR, Frontali M. Jodice C, et al. Among authors: spadaro m. Hum Mol Genet. 1997 Oct;6(11):1973-8. doi: 10.1093/hmg/6.11.1973. Hum Mol Genet. 1997. PMID: 9302278

5

Spinocerebellar ataxia (SCA1) in two large Italian kindreds: evidence in favour of a locus position distal to GLO1 and the HLA cluster.

Frontali M, Iodice C, Lulli P, Spadaro M, Cappellacci S, Giunti P, Malaspina P, Morellini M, Morocutti C, Novelletto A. Frontali M, et al. Among authors: spadaro m. Ann Hum Genet. 1991 Jan;55(1):7-15. doi: 10.1111/j.1469-1809.1991.tb00393.x. Ann Hum Genet. 1991. PMID: 1675045

6

[Clinical study of two families with late-onset autosomal dominant spinal-cerebellar ataxia linked with HLA. Preliminary results].

Giunti P, Spadaro M, Frontali M, Bianco F, Morocutti C. Giunti P, et al. Among authors: spadaro m. Riv Neurol. 1990 Sep-Oct;60(5):176-9. Riv Neurol. 1990. PMID: 2100035 Italian.

7

Clinical study of large kindreds with autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) of late onset.

Spadaro M, Giunti P, Colazza GB, Naso F, Bianco F, Morocutti C. Spadaro M, et al. Ital J Neurol Sci. 1993 Jan;14(1):17-21. doi: 10.1007/BF02339038. Ital J Neurol Sci. 1993. PMID: 8473149

8

Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2.

Guida S, Trettel F, Pagnutti S, Mantuano E, Tottene A, Veneziano L, Fellin T, Spadaro M, Stauderman K, Williams M, Volsen S, Ophoff R, Frants R, Jodice C, Frontali M, Pietrobon D. Guida S, et al. Among authors: spadaro m. Am J Hum Genet. 2001 Mar;68(3):759-64. doi: 10.1086/318804. Epub 2001 Feb 1. Am J Hum Genet. 2001. PMID: 11179022 Free PMC article.

9

Clusters of non-truncating mutations of P/Q type Ca2+ channel subunit Ca(v)2.1 causing episodic ataxia 2.

Mantuano E, Veneziano L, Spadaro M, Giunti P, Guida S, Leggio MG, Verriello L, Wood N, Jodice C, Frontali M. Mantuano E, et al. Among authors: spadaro m. J Med Genet. 2004 Jun;41(6):e82. doi: 10.1136/jmg.2003.015396. J Med Genet. 2004. PMID: 15173248 Free PMC article. No abstract available.

10

Autosomal dominant pure cerebellar ataxia. Neurological and genetic study.

Frontali M, Spadaro M, Giunti P, Bianco F, Jodice C, Persichetti F, Colazza GB, Lulli P, Terrenato L, Morocutti C. Frontali M, et al. Among authors: spadaro m. Brain. 1992 Dec;115 ( Pt 6):1647-54. doi: 10.1093/brain/115.6.1647. Brain. 1992. PMID: 1486455

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