Frontali M - Search Results

1

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: frontali 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.

2

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. Brain. 1992 Dec;115 ( Pt 6):1647-54. doi: 10.1093/brain/115.6.1647. Brain. 1992. PMID: 1486455

3

HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindreds.

Spadaro M, Giunti P, Lulli P, Frontali M, Jodice C, Cappellacci S, Morellini M, Persichetti F, Trabace S, Anastasi R, et al. Spadaro M, et al. Among authors: frontali m. Acta Neurol Scand. 1992 Apr;85(4):257-65. doi: 10.1111/j.1600-0404.1992.tb04041.x. Acta Neurol Scand. 1992. PMID: 1585797

4

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. Ann Hum Genet. 1991 Jan;55(1):7-15. doi: 10.1111/j.1469-1809.1991.tb00393.x. Ann Hum Genet. 1991. PMID: 1675045

5

[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: frontali m. Riv Neurol. 1990 Sep-Oct;60(5):176-9. Riv Neurol. 1990. PMID: 2100035 Italian.

6

The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias.

Giunti P, Sweeney MG, Spadaro M, Jodice C, Novelletto A, Malaspina P, Frontali M, Harding AE. Giunti P, et al. Among authors: frontali m. Brain. 1994 Aug;117 ( Pt 4):645-9. doi: 10.1093/brain/117.4.645. Brain. 1994. PMID: 7922453 Free article.

7

The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus.

Kwiatkowski TJ Jr, Orr HT, Banfi S, McCall AE, Jodice C, Persichetti F, Novelletto A, LeBorgne-DeMarquoy F, Duvick LA, Frontali M, et al. Kwiatkowski TJ Jr, et al. Among authors: frontali m. Am J Hum Genet. 1993 Aug;53(2):391-400. Am J Hum Genet. 1993. PMID: 8101039 Free PMC article.

8

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: frontali m. Am J Hum Genet. 1994 Jun;54(6):959-65. Am J Hum Genet. 1994. PMID: 8198139 Free PMC article.

9

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: frontali m. Hum Mol Genet. 1993 Sep;2(9):1383-7. doi: 10.1093/hmg/2.9.1383. Hum Mol Genet. 1993. PMID: 8242061

10

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. 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.

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