Spano A - Search Results

1

Celiac disease in patients with sporadic and inherited cardiomyopathies and in their relatives.

Not T, Faleschini E, Tommasini A, Repetto A, Pasotti M, Baldas V, Spano A, Sblattero D, Marzari R, Campana C, Gavazzi A, Tavazzi L, Biagi F, Roberto Corazza G, Ventura A, Arbustini E. Not T, et al. Among authors: spano a. Eur Heart J. 2003 Aug;24(15):1455-61. doi: 10.1016/s0195-668x(03)00310-5. Eur Heart J. 2003. PMID: 12909075

2

Mass screening for coeliac disease using antihuman transglutaminase antibody assay.

Tommasini A, Not T, Kiren V, Baldas V, Santon D, Trevisiol C, Berti I, Neri E, Gerarduzzi T, Bruno I, Lenhardt A, Zamuner E, Spanò A, Crovella S, Martellossi S, Torre G, Sblattero D, Marzari R, Bradbury A, Tamburlini G, Ventura A. Tommasini A, et al. Among authors: spano a. Arch Dis Child. 2004 Jun;89(6):512-5. doi: 10.1136/adc.2003.029603. Arch Dis Child. 2004. PMID: 15155392 Free PMC article.

3

A reliable screening procedure for coeliac disease in clinical practice.

Trevisiol C, Ventura A, Baldas V, Tommasini A, Santon D, Martelossi S, Torre G, Berti I, Spanò A, Crovella S, Amoroso A, Sblattero D, Marzari R, Bradbury A, Not T. Trevisiol C, et al. Among authors: spano a. Scand J Gastroenterol. 2002 Jun;37(6):679-84. doi: 10.1080/00365520212513. Scand J Gastroenterol. 2002. PMID: 12126246

4

Variant mannose-binding lectin alleles are associated with celiac disease.

Boniotto M, Braida L, Spanò A, Pirulli D, Baldas V, Trevisiol C, Not T, Tommasini A, Amoroso A, Crovella S. Boniotto M, et al. Among authors: spano a. Immunogenetics. 2002 Nov;54(8):596-8. doi: 10.1007/s00251-002-0504-2. Epub 2002 Oct 9. Immunogenetics. 2002. PMID: 12439623

5

Polymorphisms in the promoter region and at codon 54 of the MBL2 gene are not associated with IgA nephropathy.

Pirulli D, Boniotto M, Vatta L, Crovella S, Spano A, Morgutti M, Zezlina S, Bertola L, Roccatello D, Scolari F, Peruzzi L, Savoldi S, Amoroso A. Pirulli D, et al. Among authors: spano a. Nephrol Dial Transplant. 2001 Apr;16(4):759-64. doi: 10.1093/ndt/16.4.759. Nephrol Dial Transplant. 2001. PMID: 11274270

6

AGXT gene mutations and their influence on clinical heterogeneity of type 1 primary hyperoxaluria.

Amoroso A, Pirulli D, Florian F, Puzzer D, Boniotto M, Crovella S, Zezlina S, Spanò A, Mazzola G, Savoldi S, Ferrettini C, Berutti S, Petrarulo M, Marangella M. Amoroso A, et al. Among authors: spano a. J Am Soc Nephrol. 2001 Oct;12(10):2072-2079. doi: 10.1681/ASN.V12102072. J Am Soc Nephrol. 2001. PMID: 11562405

7

Beta-defensin 1 gene variability among non-human primates.

Del Pero M, Boniotto M, Zuccon D, Cervella P, Spanò A, Amoroso A, Crovella S. Del Pero M, et al. Among authors: spano a. Immunogenetics. 2002 Feb;53(10-11):907-13. doi: 10.1007/s00251-001-0412-x. Epub 2002 Jan 24. Immunogenetics. 2002. PMID: 11862391

8

Polymorphisms in the MBL2 promoter correlated with risk of HIV-1 vertical transmission and AIDS progression.

Boniotto M, Crovella S, Pirulli D, Scarlatti G, Spanò A, Vatta L, Zezlina S, Tovo PA, Palomba E, Amoroso A. Boniotto M, et al. Among authors: spano a. Genes Immun. 2000 Jun;1(5):346-8. doi: 10.1038/sj.gene.6363685. Genes Immun. 2000. PMID: 11196698

9

Detection of AGXT bgene mutations by denaturing high-performance liquid chromatography for diagnosis of hyperoxaluria type 1.

Pirulli D, Giordano M, Lessi M, Spanò A, Puzzer D, Zezlina S, Boniotto M, Crovella S, Florian F, Marangella M, Momigliano-Richiardi P, Savoldi S, Amoroso A. Pirulli D, et al. Among authors: spano a. Clin Exp Med. 2001 Jun;1(2):99-104. doi: 10.1007/s10238-001-8019-y. Clin Exp Med. 2001. PMID: 11699734

10

Detection of MRP1 mRNA in human tumors and tumor cell lines by in situ RT-PCR.

Pascolo L, Fernetti C, Pirulli D, Bogoni S, Garcia-Mediavilla MV, Spanò A, Puzzer D, Tiribelli C, Amoroso A, Crovella S. Pascolo L, et al. Among authors: spano a. Biochem Biophys Res Commun. 2000 Aug 28;275(2):466-71. doi: 10.1006/bbrc.2000.3339. Biochem Biophys Res Commun. 2000. PMID: 10964688

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