Mariotti C - Search Results

1

Visual system involvement in patients with Friedreich's ataxia.

Fortuna F, Barboni P, Liguori R, Valentino ML, Savini G, Gellera C, Mariotti C, Rizzo G, Tonon C, Manners D, Lodi R, Sadun AA, Carelli V. Fortuna F, et al. Among authors: mariotti c. Brain. 2009 Jan;132(Pt 1):116-23. doi: 10.1093/brain/awn269. Epub 2008 Oct 18. Brain. 2009. PMID: 18931386

2

Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.

Pareyson D, Gellera C, Castellotti B, Antonelli A, Riggio MC, Mazzucchelli F, Girotti F, Pietrini V, Mariotti C, Di Donato S. Pareyson D, et al. Among authors: mariotti c. J Neurol. 1999 May;246(5):389-93. doi: 10.1007/s004150050369. J Neurol. 1999. PMID: 10399872

3

Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian families.

Filla A, Mariotti C, Caruso G, Coppola G, Cocozza S, Castaldo I, Calabrese O, Salvatore E, De Michele G, Riggio MC, Pareyson D, Gellera C, Di Donato S. Filla A, et al. Among authors: mariotti c. Eur Neurol. 2000;44(1):31-6. doi: 10.1159/000008189. Eur Neurol. 2000. PMID: 10894992

4

Atypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysis.

Squitieri F, Berardelli A, Nargi E, Castellotti B, Mariotti C, Cannella M, Lavitrano ML, de Grazia U, Gellera C, Ruggieri S. Squitieri F, et al. Among authors: mariotti c. Clin Genet. 2000 Jul;58(1):50-6. doi: 10.1034/j.1399-0004.2000.580108.x. Clin Genet. 2000. PMID: 10945661

5

Pathogenic effect of an intermediate-size SCA-6 allele (CAG)(19) in a homozygous patient.

Mariotti C, Gellera C, Grisoli M, Mineri R, Castucci A, Di Donato S. Mariotti C, et al. Neurology. 2001 Oct 23;57(8):1502-4. doi: 10.1212/wnl.57.8.1502. Neurology. 2001. PMID: 11673601

6

The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias.

Di Donato S, Gellera C, Mariotti C. Di Donato S, et al. Among authors: mariotti c. Neurol Sci. 2001 Jun;22(3):219-28. doi: 10.1007/s100720100017. Neurol Sci. 2001. PMID: 11731874 Review.

7

Myoclonic dystonia as unique presentation of isolated vitamin E deficiency in a young patient.

Angelini L, Erba A, Mariotti C, Gellera C, Ciano C, Nardocci N. Angelini L, et al. Among authors: mariotti c. Mov Disord. 2002 May;17(3):612-4. doi: 10.1002/mds.10026. Mov Disord. 2002. PMID: 12112220

8

Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course.

Squitieri F, Gellera C, Cannella M, Mariotti C, Cislaghi G, Rubinsztein DC, Almqvist EW, Turner D, Bachoud-Lévi AC, Simpson SA, Delatycki M, Maglione V, Hayden MR, Donato SD. Squitieri F, et al. Among authors: mariotti c. Brain. 2003 Apr;126(Pt 4):946-55. doi: 10.1093/brain/awg077. Brain. 2003. PMID: 12615650

9

Idebenone treatment in Friedreich patients: one-year-long randomized placebo-controlled trial.

Mariotti C, Solari A, Torta D, Marano L, Fiorentini C, Di Donato S. Mariotti C, et al. Neurology. 2003 May 27;60(10):1676-9. doi: 10.1212/01.wnl.0000055872.50364.fc. Neurology. 2003. PMID: 12771264 Clinical Trial.

10

Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.

Brusco A, Gellera C, Cagnoli C, Saluto A, Castucci A, Michielotto C, Fetoni V, Mariotti C, Migone N, Di Donato S, Taroni F. Brusco A, et al. Among authors: mariotti c. Arch Neurol. 2004 May;61(5):727-33. doi: 10.1001/archneur.61.5.727. Arch Neurol. 2004. PMID: 15148151

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