Cocozza S - Search Results

1

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

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

Isolation of a new gene in the Friedreich ataxia candidate region on human chromosome 9 by cDNA direct selection.

Pandolfo M, Pizzuti A, Redolfi E, Munaro M, Di Donato S, Cavalcanti F, Filla A, Monticelli A, Pianese L, Cocozza S. Pandolfo M, et al. Among authors: cocozza s. Biochem Med Metab Biol. 1994 Aug;52(2):115-9. doi: 10.1006/bmmb.1994.1041. Biochem Med Metab Biol. 1994. PMID: 7993657

4

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.

5

A dinucleotide repeat polymorphism (D9S202) in the Friedreich's ataxia region on chromosome 9q13-q21.1.

Pandolfo M, Munaro M, Cocozza S, Redolfi EM, Pianese L, Cavalcanti F, Monticelli A, Di Donato S. Pandolfo M, et al. Among authors: cocozza s. Hum Mol Genet. 1993 Jun;2(6):822. doi: 10.1093/hmg/2.6.822. Hum Mol Genet. 1993. PMID: 8353506 No abstract available.

6

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

7

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.

Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M. Campuzano V, et al. Among authors: cocozza s. Science. 1996 Mar 8;271(5254):1423-7. doi: 10.1126/science.271.5254.1423. Science. 1996. PMID: 8596916

8

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.

9

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

10

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

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