Cocozza S - Search Results

1

De Michele G, Salvatore E, Cocozza S, Filla A, Santorelli FM. De Michele G, et al. Among authors: cocozza s. Neurogenetics. 2020 Apr;21(2):145-146. doi: 10.1007/s10048-020-00603-8. Epub 2020 Feb 3. Neurogenetics. 2020. PMID: 32009217 No abstract available.

2

Linkage disequilibrium analysis of Friedreich's ataxia in 140 Caucasian families: positioning of the disease locus and evaluation of allelic heterogeneity.

Sirugo G, Cocozza S, Brice A, Cavalcanti F, De Michele G, Dones I, Filla A, Koenig M, Lorenzetti D, Monticelli A, et al. Sirugo G, et al. Among authors: cocozza s. Eur J Hum Genet. 1993;1(2):133-43. doi: 10.1159/000472400. Eur J Hum Genet. 1993. PMID: 7914465

3

Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian population.

Pianese L, Cocozza S, Campanella G, Castaldo I, Cavalcanti F, De Michele G, Filla A, Monticelli A, Munaro M, Redolfi E, et al. Pianese L, et al. Among authors: cocozza s. J Med Genet. 1994 Feb;31(2):133-5. doi: 10.1136/jmg.31.2.133. J Med Genet. 1994. PMID: 8182719 Free PMC article.

4

Evidence of a genetic marker associated with early onset in Friedreich's ataxia.

Cocozza S, Antonelli A, Campanella G, Cavalcanti F, De Michele G, Di Donato S, Filla A, Monticelli A, Pianese L, Piccinelli A, et al. Cocozza S, et al. J Neurol. 1993;240(4):254-6. doi: 10.1007/BF00818715. J Neurol. 1993. PMID: 8496716

5

Childhood onset of Friedreich ataxia: a clinical and genetic study of 36 cases.

De Michele G, Di Maio L, Filla A, Majello M, Cocozza S, Cavalcanti F, Mirante E, Campanella G. De Michele G, et al. Among authors: cocozza s. Neuropediatrics. 1996 Feb;27(1):3-7. doi: 10.1055/s-2007-973740. Neuropediatrics. 1996. PMID: 8677022

6

The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia.

Filla A, De Michele G, Cavalcanti F, Pianese L, Monticelli A, Campanella G, Cocozza S. Filla A, et al. Among authors: cocozza s. Am J Hum Genet. 1996 Sep;59(3):554-60. Am J Hum Genet. 1996. PMID: 8751856 Free PMC article.

7

Autosomal dominant cerebellar ataxia type I: multimodal electrophysiological study and comparison between SCA1 and SCA2 patients.

Perretti A, Santoro L, Lanzillo B, Filla A, De Michele G, Barbieri F, Martino G, Ragno M, Cocozza S, Caruso G. Perretti A, et al. Among authors: cocozza s. J Neurol Sci. 1996 Oct;142(1-2):45-53. doi: 10.1016/0022-510x(96)00140-2. J Neurol Sci. 1996. PMID: 8902719

8

Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes.

Filla A, De Michele G, Campanella G, Perretti A, Santoro L, Serlenga L, Ragno M, Calabrese O, Castaldo I, De Joanna G, Cocozza S. Filla A, et al. Among authors: cocozza s. J Neurol Sci. 1996 Oct;142(1-2):140-7. doi: 10.1016/0022-510x(96)00177-3. J Neurol Sci. 1996. PMID: 8902734

9

The effect of parental gender on the GAA dynamic mutation in the FRDA gene.

Pianese L, Cavalcanti F, De Michele G, Filla A, Campanella G, Calabrese O, Castaldo I, Monticelli A, Cocozza S. Pianese L, et al. Among authors: cocozza s. Am J Hum Genet. 1997 Feb;60(2):460-3. Am J Hum Genet. 1997. PMID: 9012421 Free PMC article. No abstract available.

10

Genetic abnormalities in Friedreich's ataxia.

Filla A, De Michele G, Cocozza S. Filla A, et al. Among authors: cocozza s. N Engl J Med. 1997 Apr 3;336(14):1021-2; author reply 1022. N Engl J Med. 1997. PMID: 9091786 No abstract available.

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