Pareyson D - Search Results

1

Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 families.

Mariotti C, Castellotti B, Pareyson D, Testa D, Eoli M, Antozzi C, Silani V, Marconi R, Tezzon F, Siciliano G, Marchini C, Gellera C, Donato SD. Mariotti C, et al. Among authors: pareyson d. Neuromuscul Disord. 2000 Aug;10(6):391-7. doi: 10.1016/s0960-8966(99)00132-7. Neuromuscul Disord. 2000. PMID: 10899444

2

A multicentre follow-up study of 1152 patients with myasthenia gravis in Italy.

Mantegazza R, Beghi E, Pareyson D, Antozzi C, Peluchetti D, Sghirlanzoni A, Cosi V, Lombardi M, Piccolo G, Tonali P, et al. Mantegazza R, et al. Among authors: pareyson d. J Neurol. 1990 Oct;237(6):339-44. doi: 10.1007/BF00315656. J Neurol. 1990. PMID: 2277266 Clinical Trial.

3

Kennedy's disease: clinical and molecular study of two Italian families.

Pareyson D, Castellotti B, Botti S, Defanti CA, Gellera C, Taroni F, Sghirlanzoni A. Pareyson D, et al. Ital J Neurol Sci. 1995 Oct;16(7):467-71. doi: 10.1007/BF02229324. Ital J Neurol Sci. 1995. PMID: 8749704

4

Very late onset Friedreich's ataxia without cardiomyopathy is associated with limited GAA expansion in the X25 gene.

Gellera C, Pareyson D, Castellotti B, Mazzucchelli F, Zappacosta B, Pandolfo M, Di Donato S. Gellera C, et al. Among authors: pareyson d. Neurology. 1997 Oct;49(4):1153-5. doi: 10.1212/wnl.49.4.1153. Neurology. 1997. PMID: 9339708

5

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. J Neurol. 1999 May;246(5):389-93. doi: 10.1007/s004150050369. J Neurol. 1999. PMID: 10399872

6

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: pareyson d. Eur Neurol. 2000;44(1):31-6. doi: 10.1159/000008189. Eur Neurol. 2000. PMID: 10894992

7

Affective disorders and multiple sclerosis: a controlled study on 65 Italian patients.

Salmaggi A, Palumbo R, Fontanillas L, Eoli M, La Mantia L, Solari A, Pareyson D, Milanese C. Salmaggi A, et al. Among authors: pareyson d. Ital J Neurol Sci. 1998 Jun;19(3):171-5. doi: 10.1007/BF00831567. Ital J Neurol Sci. 1998. PMID: 10933472 Clinical Trial.

8

Chronic inflammatory demyelinating polyradiculoneuropathy: long-term course and treatment of 60 patients.

Sghirlanzoni A, Solari A, Ciano C, Mariotti C, Fallica E, Pareyson D. Sghirlanzoni A, et al. Among authors: pareyson d. Neurol Sci. 2000 Feb;21(1):31-7. doi: 10.1007/s100720070116. Neurol Sci. 2000. PMID: 10938200 Clinical Trial.

9

Does CMT1A homozygosity cause more severe disease with root hypertrophy and higher CSF proteins?

Pareyson D, Testa D, Morbin M, Erbetta A, Ciano C, Lauria G, Milani M, Taroni F. Pareyson D, et al. Neurology. 2003 May 27;60(10):1721-2. doi: 10.1212/01.wnl.0000059262.34846.8a. Neurology. 2003. PMID: 12771282 Free article. No abstract available.

10

Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families.

Mariotti C, Gellera C, Rimoldi M, Mineri R, Uziel G, Zorzi G, Pareyson D, Piccolo G, Gambi D, Piacentini S, Squitieri F, Capra R, Castellotti B, Di Donato S. Mariotti C, et al. Among authors: pareyson d. Neurol Sci. 2004 Jul;25(3):130-7. doi: 10.1007/s10072-004-0246-z. Neurol Sci. 2004. PMID: 15300460

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