Cocozza S - Search Results

1

Serum transferrin receptor levels in Friedreich's and other degenerative ataxias.

Scarano V, de Cristofaro T, De Michele G, Salvatore E, De Biase I, Monticelli A, Filla A, Cocozza S. Scarano V, et al. Among authors: cocozza s. Neurology. 2001 Jul 10;57(1):159-60. doi: 10.1212/wnl.57.1.159. Neurology. 2001. PMID: 11445653 No abstract available.

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

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.

4

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.

5

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.

6

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

7

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

8

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

9

Coronary heart disease, echo-Doppler evidence of peripheral arterial disease and polymorphism of apolipoprotein B gene and Apo AI/CIII cluster.

De Lorenzo F, Rubba P, Monticelli A, Cocozza S. De Lorenzo F, et al. Among authors: cocozza s. Angiology. 1993 Oct;44(10):785-90. doi: 10.1177/000331979304401004. Angiology. 1993. PMID: 8105730

10

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.

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