Cocozza S - Search Results

1

DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich ataxia patients.

Castaldo I, Pinelli M, Monticelli A, Acquaviva F, Giacchetti M, Filla A, Sacchetti S, Keller S, Avvedimento VE, Chiariotti L, Cocozza S. Castaldo I, et al. Among authors: cocozza s. J Med Genet. 2008 Dec;45(12):808-12. doi: 10.1136/jmg.2008.058594. Epub 2008 Aug 12. J Med Genet. 2008. PMID: 18697824

2

Early signs of carotid and iliac atherosclerosis in patients with severe hyperlipoproteinemia.

De Lorenzo F, De Simone B, Irace C, Carbone L, Gnasso A, Liguori M, Monticelli A, Cocozza S, Cortese C, Rubba P. De Lorenzo F, et al. Among authors: cocozza s. Int Angiol. 1992 Apr-Jun;11(2):122-6. Int Angiol. 1992. PMID: 1357042

3

Taq I RFLP in the human cellular retinol-binding protein (CRBP) gene.

Pellegrino A, Garofalo S, Cocozza S, Monticelli A, Faraonio R, Varrone S, Colantuoni V. Pellegrino A, et al. Among authors: cocozza s. Nucleic Acids Res. 1988 Aug 11;16(15):7758. doi: 10.1093/nar/16.15.7758. Nucleic Acids Res. 1988. PMID: 2901072 Free PMC article.

4

DNA polymorphism of the insulin gene, diabetes, and severe obesity.

Isernia C, Contaldo F, Scalfi L, Cocozza S, Monticelli A, Pellegrino A. Isernia C, et al. Among authors: cocozza s. Diabetes Care. 1988 Jun;11(6):511-2. doi: 10.2337/diacare.11.6.511. Diabetes Care. 1988. PMID: 3042318 No abstract available.

5

Polymorphism at the 5' end flanking region of the insulin gene is associated with reduced insulin secretion in healthy individuals.

Cocozza S, Riccardi G, Monticelli A, Capaldo B, Genovese S, Krogh V, Celentano E, Farinaro E, Varrone S, Avvedimento VE. Cocozza S, et al. Eur J Clin Invest. 1988 Dec;18(6):582-6. doi: 10.1111/j.1365-2362.1988.tb01271.x. Eur J Clin Invest. 1988. PMID: 3147185

6

Structural organization of the 3' half of the rat thyroglobulin gene.

Avvedimento VE, Musti AM, Obici S, Cocozza S, Di Lauro R. Avvedimento VE, et al. Among authors: cocozza s. Nucleic Acids Res. 1984 Apr 25;12(8):3461-72. doi: 10.1093/nar/12.8.3461. Nucleic Acids Res. 1984. PMID: 6328423 Free PMC article.

7

Early onset of coronary heart disease is associated with apo AI-CIII SstI polymorphism.

De Lorenzo F, Monticelli A, Cocozza S. De Lorenzo F, et al. Among authors: cocozza s. Aust N Z J Med. 1994 Oct;24(5):579-80. doi: 10.1111/j.1445-5994.1994.tb01766.x. Aust N Z J Med. 1994. PMID: 7848167 No abstract available.

8

SstI APO AI-CIII DNA polymorphism associated with lower levels of HDL cholesterol in a young population from south of Italy.

De Lorenzo F, Monticelli A, Cocozza S. De Lorenzo F, et al. Among authors: cocozza s. Aust N Z J Med. 1993 Dec;23(6):711-2. doi: 10.1111/j.1445-5994.1993.tb04733.x. Aust N Z J Med. 1993. PMID: 7908186 No abstract available.

9

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

10

Extracoronary atherosclerosis and genetic variants of apolipoprotein AI-CIII cluster in myocardial infarction survivors from southern Italy.

De Lorenzo F, Monticelli A, Cocozza S, De Simone B, Rubba P. De Lorenzo F, et al. Among authors: cocozza s. Clin Investig. 1994 Jun;72(6):435-41. doi: 10.1007/BF00180517. Clin Investig. 1994. PMID: 7950154

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