Andria G - Search Results

1

Spina bifida and folate-related genes: a study of gene-gene interactions.

de Franchis R, Botto LD, Sebastio G, Ricci R, Iolascon A, Capra V, Andria G, Mastroiacovo P. de Franchis R, et al. Among authors: andria g. Genet Med. 2002 May-Jun;4(3):126-30. doi: 10.1097/00125817-200205000-00005. Genet Med. 2002. PMID: 12180146 Free article.

2

Analysis of seven maternal polymorphisms of genes involved in homocysteine/folate metabolism and risk of Down syndrome offspring.

Scala I, Granese B, Sellitto M, Salomè S, Sammartino A, Pepe A, Mastroiacovo P, Sebastio G, Andria G. Scala I, et al. Among authors: andria g. Genet Med. 2006 Jul;8(7):409-16. doi: 10.1097/01.gim.0000228206.21793.82. Genet Med. 2006. PMID: 16845273 Free article.

3

The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy.

de Franchis R, Buoninconti A, Mandato C, Pepe A, Sperandeo MP, Del Gado R, Capra V, Salvaggio E, Andria G, Mastroiacovo P. de Franchis R, et al. Among authors: andria g. J Med Genet. 1998 Dec;35(12):1009-13. doi: 10.1136/jmg.35.12.1009. J Med Genet. 1998. PMID: 9863598 Free PMC article.

4

The molecular basis of homocystinuria due to cystathionine beta-synthase deficiency in Italian families, and report of four novel mutations.

Sebastio G, Sperandeo MP, Panico M, de Franchis R, Kraus JP, Andria G. Sebastio G, et al. Among authors: andria g. Am J Hum Genet. 1995 Jun;56(6):1324-33. Am J Hum Genet. 1995. PMID: 7762555 Free PMC article.

5

Spina bifida, 677T-->C mutation, and role of folate.

de Franchis R, Sebastio G, Mandato C, Andria G, Mastroiacovo P. de Franchis R, et al. Among authors: andria g. Lancet. 1995 Dec 23-30;346(8991-8992):1703. doi: 10.1016/s0140-6736(95)92865-0. Lancet. 1995. PMID: 8551837 No abstract available.

6

Clinical aspects of cystathionine beta-synthase deficiency: how wide is the spectrum? The Italian Collaborative Study Group on Homocystinuria.

De Franchis R, Sperandeo MP, Sebastio G, Andria G. De Franchis R, et al. Among authors: andria g. Eur J Pediatr. 1998 Apr;157 Suppl 2:S67-70. doi: 10.1007/pl00014309. Eur J Pediatr. 1998. PMID: 9587029 Review.

7

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

8

Re: folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women.

Scala I, Granese B, Lisi A, Mastroiacovo P, Andria G. Scala I, et al. Among authors: andria g. Am J Med Genet A. 2007 May 1;143A(9):1015-7; discussion 1018-9. doi: 10.1002/ajmg.a.31693. Am J Med Genet A. 2007. PMID: 17431899 No abstract available.

9

Lysinuric protein intolerance: update and extended mutation analysis of the SLC7A7 gene.

Sperandeo MP, Andria G, Sebastio G. Sperandeo MP, et al. Among authors: andria g. Hum Mutat. 2008 Jan;29(1):14-21. doi: 10.1002/humu.20589. Hum Mutat. 2008. PMID: 17764084 Review.

10

Lysinuric protein intolerance: reviewing concepts on a multisystem disease.

Sebastio G, Sperandeo MP, Andria G. Sebastio G, et al. Among authors: andria g. Am J Med Genet C Semin Med Genet. 2011 Feb 15;157C(1):54-62. doi: 10.1002/ajmg.c.30287. Epub 2011 Feb 9. Am J Med Genet C Semin Med Genet. 2011. PMID: 21308987 Review.

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