Dessì V - Search Results

1

Improvement of prenatal diagnosis of Wilson disease using microsatellite markers.

Loudianos G, Figus AL, Loi A, Angius A, Dessì V, Deiana M, De Virgiliis S, Monni G, Cao A, Pirastu M. Loudianos G, et al. Among authors: dessi v. Prenat Diagn. 1994 Oct;14(10):999-1002. doi: 10.1002/pd.1970141018. Prenat Diagn. 1994. PMID: 7899276

2

Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populations.

Figus A, Angius A, Loudianos G, Bertini C, Dessi V, Loi A, Deiana M, Lovicu M, Olla N, Sole G, et al. Figus A, et al. Among authors: dessi v. Am J Hum Genet. 1995 Dec;57(6):1318-24. Am J Hum Genet. 1995. PMID: 8533760 Free PMC article.

3

Wilson disease mutations associated with uncommon haplotypes in Mediterranean patients.

Loudianos G, Dessì V, Angius A, Lovicu M, Loi A, Deiana M, Akar N, Vajro P, Figus A, Cao A, Pirastu M. Loudianos G, et al. Among authors: dessi v. Hum Genet. 1996 Dec;98(6):640-2. doi: 10.1007/s004390050275. Hum Genet. 1996. PMID: 8931691

4

Further delineation of the molecular pathology of Wilson disease in the Mediterranean population.

Loudianos G, Dessì V, Lovicu M, Angius A, Nurchi A, Sturniolo GC, Marcellini M, Zancan L, Bragetti P, Akar N, Yagci R, Vegnente A, Cao A, Pirastu M. Loudianos G, et al. Among authors: dessi v. Hum Mutat. 1998;12(2):89-94. doi: 10.1002/(SICI)1098-1004(1998)12:2<89::AID-HUMU3>3.0.CO;2-G. Hum Mutat. 1998. PMID: 9671269

5

Haplotype and mutation analysis in Greek patients with Wilson disease.

Loudianos G, Dessì V, Lovicu M, Angius A, Kanavakis E, Tzetis M, Kattamis C, Manolaki N, Vassiliki G, Karpathios T, Cao A, Pirastu M. Loudianos G, et al. Among authors: dessi v. Eur J Hum Genet. 1998 Sep-Oct;6(5):487-91. doi: 10.1038/sj.ejhg.5200219. Eur J Hum Genet. 1998. PMID: 9801873

6

Molecular characterization of wilson disease in the Sardinian population--evidence of a founder effect.

Loudianos G, Dessi V, Lovicu M, Angius A, Figus A, Lilliu F, De Virgiliis S, Nurchi AM, Deplano A, Moi P, Pirastu M, Cao A. Loudianos G, et al. Among authors: dessi v. Hum Mutat. 1999;14(4):294-303. doi: 10.1002/(SICI)1098-1004(199910)14:4<294::AID-HUMU4>3.0.CO;2-9. Hum Mutat. 1999. PMID: 10502776

7

Mutation analysis in patients of Mediterranean descent with Wilson disease: identification of 19 novel mutations.

Loudianos G, Dessi V, Lovicu M, Angius A, Altuntas B, Giacchino R, Marazzi M, Marcellini M, Sartorelli MR, Sturniolo GC, Kocak N, Yuce A, Akar N, Pirastu M, Cao A. Loudianos G, et al. Among authors: dessi v. J Med Genet. 1999 Nov;36(11):833-6. J Med Genet. 1999. PMID: 10544227 Free PMC article.

8

Twenty-four novel mutations in Wilson disease patients of predominantly Italian origin.

Lepori MB, Lovicu M, Dessi V, Zappu A, Incollu S, Zancan L, Giacchino R, Iorio R, Vajro P, Maggiore G, Marcellini M, Barbera C, Pellecchia MT, Simonetti R, Kostic V, Farci AM, Solinas A, De Virgiliis S, Cao A, Loudianos G. Lepori MB, et al. Among authors: dessi v. Genet Test. 2007 Fall;11(3):328-32. doi: 10.1089/gte.2007.0015. Genet Test. 2007. PMID: 17949296

9

RNA analysis of consensus sequence splicing mutations: implications for the diagnosis of Wilson disease.

Lovicu M, Lepori MB, Incollu S, Dessì V, Zappu A, Iorio R, D'Ambrosi M, Pellecchia MT, Barone P, Maggiore G, De Virgiliis S, Cao A, Loudianos G. Lovicu M, et al. Among authors: dessi v. Genet Test Mol Biomarkers. 2009 Apr;13(2):185-91. doi: 10.1089/gtmb.2008.0089. Genet Test Mol Biomarkers. 2009. PMID: 19371217

10

Wilson's disease in two consecutive generations: the detection of three mutated alleles in the ATP7B gene in two Sardinian families.

Loudianos G, Zappu A, Lepori MB, Incollu S, Dessì V, Mameli E, Garrucciu G, De Virgiliis S, Cao A. Loudianos G, et al. Among authors: dessi v. Dig Liver Dis. 2013 Apr;45(4):342-5. doi: 10.1016/j.dld.2012.10.017. Epub 2012 Dec 7. Dig Liver Dis. 2013. PMID: 23219664

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