Andria G - Search Results

1

In vivo platelet activation in homozygous cystathionine beta-synthase deficiency: a probucol-sensitive phenomenon.

Di Minno G, Margaglione M, Cirillo F, Grandone E, Davì G, Ciabattoni G, Catalano I, Strisciuglio P, Andria G, Coppola A, et al. Di Minno G, et al. Among authors: andria g. Trans Assoc Am Physicians. 1992;105:149-56. Trans Assoc Am Physicians. 1992. PMID: 1308991 No abstract available.

2

Abnormally high thromboxane biosynthesis in homozygous homocystinuria. Evidence for platelet involvement and probucol-sensitive mechanism.

Di Minno G, Davì G, Margaglione M, Cirillo F, Grandone E, Ciabattoni G, Catalano I, Strisciuglio P, Andria G, Patrono C, et al. Di Minno G, et al. Among authors: andria g. J Clin Invest. 1993 Sep;92(3):1400-6. doi: 10.1172/JCI116715. J Clin Invest. 1993. PMID: 8376592 Free PMC article.

3

Oxidative stress and platelet activation in homozygous homocystinuria.

Davì G, Di Minno G, Coppola A, Andria G, Cerbone AM, Madonna P, Tufano A, Falco A, Marchesani P, Ciabattoni G, Patrono C. Davì G, et al. Among authors: andria g. Circulation. 2001 Sep 4;104(10):1124-8. doi: 10.1161/hc3501.095287. Circulation. 2001. PMID: 11535567 Clinical Trial.

4

Early signs of vascular disease in homocystinuria: a noninvasive study by ultrasound methods in eight families with cystathionine-beta-synthase deficiency.

Rubba P, Faccenda F, Pauciullo P, Carbone L, Mancini M, Strisciuglio P, Carrozzo R, Sartorio R, del Giudice E, Andria G. Rubba P, et al. Among authors: andria g. Metabolism. 1990 Nov;39(11):1191-5. doi: 10.1016/0026-0495(90)90093-r. Metabolism. 1990. PMID: 2233281

5

Contribution of the cystathionine beta-synthase gene (844ins68) polymorphism to the risk of early-onset venous and arterial occlusive disease and of fasting hyperhomocysteinemia.

de Franchis R, Fermo I, Mazzola G, Sebastio G, Di Minno G, Coppola A, Andria G, D'Angelo A. de Franchis R, et al. Among authors: andria g. Thromb Haemost. 2000 Oct;84(4):576-82. Thromb Haemost. 2000. PMID: 11057853

6

Dietary treatment of liver glycogenosis.

Andria G, Parenti G, Strisciuglio P, Tinello C. Andria G, et al. Beitr Infusionsther. 1991;27:161-9. Beitr Infusionsther. 1991. PMID: 1713097 Review. No abstract available.

7

Aldolase B mutations in Italian families affected by hereditary fructose intolerance.

Sebastio G, de Franchis R, Strisciuglio P, Andria G, Dionisi Vici C, Sabetta G, Gatti R, Cross NC, Cox TM. Sebastio G, et al. Among authors: andria g. J Med Genet. 1991 Apr;28(4):241-3. doi: 10.1136/jmg.28.4.241. J Med Genet. 1991. PMID: 1856829 Free PMC article.

8

Ultrasonographic detection of arterial disease in treated homocystinuria.

Rubba P, Faccenda F, Strisciuglio P, Andria G. Rubba P, et al. Among authors: andria g. N Engl J Med. 1989 Dec 21;321(25):1759-60. doi: 10.1056/NEJM198912213212514. N Engl J Med. 1989. PMID: 2687690 No abstract available.

9

Multisystem triglyceride storage disease is due to a specific defect in the degradation of endocellularly synthesized triglycerides.

Di Donato S, Garavaglia B, Strisciuglio P, Borrone C, Andria G. Di Donato S, et al. Among authors: andria g. Neurology. 1988 Jul;38(7):1107-10. doi: 10.1212/wnl.38.7.1107. Neurology. 1988. PMID: 3386830

10

Centric fission of chromosome 9 in a boy with trisomy 9p.

Concolino D, Cinti R, Moricca M, Andria G, Strisciuglio P. Concolino D, et al. Among authors: andria g. Am J Med Genet. 1998 Aug 27;79(1):35-7. doi: 10.1002/(sici)1096-8628(19980827)79:1<35::aid-ajmg9>3.0.co;2-h. Am J Med Genet. 1998. PMID: 9738866

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