Rossetti LC - Search Results

1

Analysis of factor VIII gene intron 1 inversion in Argentinian families with severe haemophilia A and a review of the literature.

Rossetti LC, Candela M, Bianco RP, de Tezanos Pinto M, Western A, Goodeve A, Larripa IB, De Brasi CD. Rossetti LC, et al. Blood Coagul Fibrinolysis. 2004 Oct;15(7):569-72. doi: 10.1097/00001721-200410000-00006. Blood Coagul Fibrinolysis. 2004. PMID: 15389123

2

Rapid genotyping of XbaI and MspI DNA polymorphisms of the human factor VIII gene: estimation of their combined heterozygosity in the Argentinean population.

De Brasi CD, Rossetti LC, Larripa IB. De Brasi CD, et al. Among authors: rossetti lc. Haematologica. 2003 Feb;88(2):232-4. Haematologica. 2003. PMID: 12604420 No abstract available.

3

Homeologous recombination between AluSx-sequences as a cause of hemophilia.

Rossetti LC, Goodeve A, Larripa IB, De Brasi CD. Rossetti LC, et al. Hum Mutat. 2004 Nov;24(5):440. doi: 10.1002/humu.9288. Hum Mutat. 2004. PMID: 15459970

4

Genotyping the hemophilia inversion hotspot by use of inverse PCR.

Rossetti LC, Radic CP, Larripa IB, De Brasi CD. Rossetti LC, et al. Clin Chem. 2005 Jul;51(7):1154-8. doi: 10.1373/clinchem.2004.046490. Epub 2005 Apr 28. Clin Chem. 2005. PMID: 15860568

5

Sixteen novel hemophilia A causative mutations in the first Argentinian series of severe molecular defects.

Rossetti LC, Radic CP, Candela M, Pérez Bianco R, de Tezanos Pinto M, Goodeve A, Larripa IB, De Brasi CD. Rossetti LC, et al. Haematologica. 2007 Jun;92(6):842-5. doi: 10.3324/haematol.11112. Haematologica. 2007. PMID: 17550859 Free article.

6

Developing a new generation of tests for genotyping hemophilia-causative rearrangements involving int22h and int1h hotspots in the factor VIII gene.

Rossetti LC, Radic CP, Larripa IB, De Brasi CD. Rossetti LC, et al. J Thromb Haemost. 2008 May;6(5):830-6. doi: 10.1111/j.1538-7836.2008.02926.x. Epub 2008 Feb 12. J Thromb Haemost. 2008. PMID: 18284600 Free article.

7

Inverse shifting PCR based prenatal diagnosis of hemophilia-causative inversions involving int22h and int1h hotspots from chorionic villus samples.

Radic CP, Rossetti LC, Zuccoli JR, Abelleyro MM, Larripa IB, De Brasi CD. Radic CP, et al. Among authors: rossetti lc. Prenat Diagn. 2009 Dec;29(12):1183-5. doi: 10.1002/pd.2393. Prenat Diagn. 2009. PMID: 19842127 No abstract available.

8

Informativeness of a novel multiallelic marker-set comprising an F8 intron 21 and three tightly linked loci for haemophilia A carriership analysis.

Machado FB, Alves Da Silva AF, Rossetti LC, De Brasi CD, Medina-Acosta E. Machado FB, et al. Among authors: rossetti lc. Haemophilia. 2011 Mar;17(2):257-66. doi: 10.1111/j.1365-2516.2010.02404.x. Epub 2010 Nov 11. Haemophilia. 2011. PMID: 21070487

9

Are int22h-mediated deletions a common cause of hemophilia?

Abelleyro MM, Rossetti LC, Radic CP, Candela M, Larripa IB, De Brasi CD. Abelleyro MM, et al. Among authors: rossetti lc. Ann Hematol. 2012 Apr;91(4):633-6. doi: 10.1007/s00277-011-1295-z. Epub 2011 Jul 20. Ann Hematol. 2012. PMID: 21773729 No abstract available.

10

Eighteen years of molecular genotyping the hemophilia inversion hotspot: from southern blot to inverse shifting-PCR.

Rossetti LC, Radic CP, Abelleyro MM, Larripa IB, De Brasi CD. Rossetti LC, et al. Int J Mol Sci. 2011;12(10):7271-85. doi: 10.3390/ijms12107271. Epub 2011 Oct 24. Int J Mol Sci. 2011. PMID: 22072947 Free PMC article. Review.

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