Frontali M - Search Results

1

Riluzole in patients with hereditary cerebellar ataxia: a randomised, double-blind, placebo-controlled trial.

Romano S, Coarelli G, Marcotulli C, Leonardi L, Piccolo F, Spadaro M, Frontali M, Ferraldeschi M, Vulpiani MC, Ponzelli F, Salvetti M, Orzi F, Petrucci A, Vanacore N, Casali C, Ristori G. Romano S, et al. Among authors: frontali m. Lancet Neurol. 2015 Oct;14(10):985-91. doi: 10.1016/S1474-4422(15)00201-X. Epub 2015 Aug 25. Lancet Neurol. 2015. PMID: 26321318 Clinical Trial.

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

[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.

5

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.

6

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.

7

A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs.

Spadaro M, Ursu S, Lehmann-Horn F, Veneziano L, Antonini G, Giunti P, Frontali M, Jurkat-Rott K. Spadaro M, et al. Among authors: frontali m. Neurogenetics. 2004 Sep;5(3):177-85. doi: 10.1007/s10048-004-0183-2. Epub 2004 Jul 31. Neurogenetics. 2004. PMID: 15459825

8

Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2.

Mantuano E, Romano S, Veneziano L, Gellera C, Castellotti B, Caimi S, Testa D, Estienne M, Zorzi G, Bugiani M, Rajabally YA, Barcina MJ, Servidei S, Panico A, Frontali M, Mariotti C. Mantuano E, et al. Among authors: frontali m. J Neurol Sci. 2010 Apr 15;291(1-2):30-6. doi: 10.1016/j.jns.2010.01.010. Epub 2010 Feb 2. J Neurol Sci. 2010. PMID: 20129625

9

Riluzole in cerebellar ataxia: a randomized, double-blind, placebo-controlled pilot trial.

Ristori G, Romano S, Visconti A, Cannoni S, Spadaro M, Frontali M, Pontieri FE, Vanacore N, Salvetti M. Ristori G, et al. Among authors: frontali m. Neurology. 2010 Mar 9;74(10):839-45. doi: 10.1212/WNL.0b013e3181d31e23. Neurology. 2010. PMID: 20211908 Clinical Trial.

10

Fractal analysis reveals reduced complexity of retinal vessels in CADASIL.

Cavallari M, Falco T, Frontali M, Romano S, Bagnato F, Orzi F. Cavallari M, et al. Among authors: frontali m. PLoS One. 2011 Apr 27;6(4):e19150. doi: 10.1371/journal.pone.0019150. PLoS One. 2011. PMID: 21556373 Free PMC article.

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