Bafunno V - Search Results

1

Bafunno V, Margaglione M. Bafunno V, et al. Clin Chem Lab Med. 2010 Dec;48 Suppl 1:S41-51. doi: 10.1515/CCLM.2010.361. Epub 2010 Oct 29. Clin Chem Lab Med. 2010. PMID: 21034258 Review.

2

The risk of occurrence of venous thrombosis: focus on protein Z.

Bafunno V, Santacroce R, Margaglione M. Bafunno V, et al. Thromb Res. 2011 Dec;128(6):508-15. doi: 10.1016/j.thromres.2011.08.007. Epub 2011 Aug 31. Thromb Res. 2011. PMID: 21885093 Review.

3

Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A.

Bafunno V, Santacroce R, Chetta M, D'Andrea G, Pisanelli D, Sessa F, Trotta T, Tagariello G, Peyvandi F, Margaglione M. Bafunno V, et al. Haemophilia. 2010 May;16(3):469-73. doi: 10.1111/j.1365-2516.2009.02150.x. Epub 2009 Dec 14. Haemophilia. 2010. PMID: 20015215

4

Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification.

Santacroce R, Longo V, Bafunno V, Sessa F, Chetta M, Sarno M, Bukvic N, D'Andrea G, Tomaiuolo M, Margaglione M. Santacroce R, et al. Among authors: bafunno v. Genet Test Mol Biomarkers. 2009 Oct;13(5):573-6. doi: 10.1089/gtmb.2009.0015. Genet Test Mol Biomarkers. 2009. PMID: 19715469

5

Role of the M2 haplotype within the annexin A5 gene in the occurrence of pregnancy-related venous thromboembolism.

Grandone E, Tiscia G, Colaizzo D, Chinni E, Pisanelli D, Bafunno V, Margaglione M. Grandone E, et al. Among authors: bafunno v. Am J Obstet Gynecol. 2010 Nov;203(5):461.e1-5. doi: 10.1016/j.ajog.2010.06.007. Am J Obstet Gynecol. 2010. PMID: 20643388

6

Sex modulation of the occurrence of jak2 v617f mutation in patients with splanchnic venous thrombosis.

Colaizzo D, Tiscia GL, Bafunno V, Amitrano L, Vergura P, Lupone MR, Grandone E, Guardascione MA, Margaglione M. Colaizzo D, et al. Among authors: bafunno v. Thromb Res. 2011 Sep;128(3):233-6. doi: 10.1016/j.thromres.2011.03.024. Epub 2011 Apr 16. Thromb Res. 2011. PMID: 21497883

7

Fatal pulmonary thromboembolism. A retrospective autopsy study: searching for genetic thrombophilias (Factor V Leiden (G1691A) and FII (G20210A) gene variants) and dating the thrombus.

Fineschi V, Bafunno V, Bello S, De Stefano F, Margaglione M, Neri M, Riezzo I, Turillazzi E, Bonsignore A, Vecchione G, Ventura F, Grandone E. Fineschi V, et al. Among authors: bafunno v. Forensic Sci Int. 2012 Jan 10;214(1-3):152-8. doi: 10.1016/j.forsciint.2011.07.046. Epub 2011 Aug 26. Forensic Sci Int. 2012. PMID: 21871746

8

McKusick-Kaufman or Bardet-Biedl syndrome? A new borderline case in an Italian nonconsanguineous healthy family.

Chetta M, Bukvic N, Bafunno V, Sarno M, Magaldi R, Grilli G, Bertozzi V, Perfetto F, Margaglione M. Chetta M, et al. Among authors: bafunno v. Indian J Hum Genet. 2011 May;17(2):94-6. doi: 10.4103/0971-6866.86194. Indian J Hum Genet. 2011. PMID: 22090721 Free PMC article.

9

Mutational spectrum of the c1 inhibitor gene in a cohort of Italian patients with hereditary angioedema: description of nine novel mutations.

Bafunno V, Bova M, Loffredo S, Divella C, Petraroli A, Marone G, Montinaro V, Margaglione M, Triggiani M. Bafunno V, et al. Ann Hum Genet. 2014 Mar;78(2):73-82. doi: 10.1111/ahg.12052. Epub 2014 Jan 24. Ann Hum Genet. 2014. PMID: 24456027

10

Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness.

Trunzo R, Santacroce R, D'Andrea G, Longo V, De Girolamo G, Dimatteo C, Leccese A, Bafunno V, Lillo V, Papadia F, Margaglione M. Trunzo R, et al. Among authors: bafunno v. Clin Chim Acta. 2015 Oct 23;450:51-5. doi: 10.1016/j.cca.2015.07.014. Epub 2015 Jul 23. Clin Chim Acta. 2015. PMID: 26210745

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