Bellissimo DB - Search Results

1

Genetic mutations in von Willebrand disease identified by DHPLC and DNA sequence analysis.

Kakela JK, Friedman KD, Haberichter SL, Buchholz NP, Christopherson PA, Kroner PA, Gill JC, Montgomery RR, Bellissimo DB. Kakela JK, et al. Among authors: bellissimo db. Mol Genet Metab. 2006 Mar;87(3):262-71. doi: 10.1016/j.ymgme.2005.09.016. Mol Genet Metab. 2006. PMID: 16321553

2

Critical von Willebrand factor A1 domain residues influence type VI collagen binding.

Flood VH, Gill JC, Christopherson PA, Bellissimo DB, Friedman KD, Haberichter SL, Lentz SR, Montgomery RR. Flood VH, et al. Among authors: bellissimo db. J Thromb Haemost. 2012 Jul;10(7):1417-24. doi: 10.1111/j.1538-7836.2012.04746.x. J Thromb Haemost. 2012. PMID: 22507569 Free PMC article.

3

Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival.

Haberichter SL, Balistreri M, Christopherson P, Morateck P, Gavazova S, Bellissimo DB, Manco-Johnson MJ, Gill JC, Montgomery RR. Haberichter SL, et al. Among authors: bellissimo db. Blood. 2006 Nov 15;108(10):3344-51. doi: 10.1182/blood-2006-04-015065. Epub 2006 Jul 11. Blood. 2006. PMID: 16835381 Free PMC article.

4

Von Willebrand disease in the United States: a perspective from Wisconsin.

Flood VH, Gill JC, Friedman KD, Bellissimo DB, Haberichter SL, Montgomery RR. Flood VH, et al. Among authors: bellissimo db. Semin Thromb Hemost. 2011 Jul;37(5):528-34. doi: 10.1055/s-0031-1281039. Epub 2011 Nov 18. Semin Thromb Hemost. 2011. PMID: 22102196 Free PMC article. Review.

5

VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population.

Bellissimo DB, Christopherson PA, Flood VH, Gill JC, Friedman KD, Haberichter SL, Shapiro AD, Abshire TC, Leissinger C, Hoots WK, Lusher JM, Ragni MV, Montgomery RR. Bellissimo DB, et al. Blood. 2012 Mar 1;119(9):2135-40. doi: 10.1182/blood-2011-10-384610. Epub 2011 Dec 23. Blood. 2012. PMID: 22197721 Free PMC article.

6

Crucial role for the VWF A1 domain in binding to type IV collagen.

Flood VH, Schlauderaff AC, Haberichter SL, Slobodianuk TL, Jacobi PM, Bellissimo DB, Christopherson PA, Friedman KD, Gill JC, Hoffmann RG, Montgomery RR; Zimmerman Program Investigators. Flood VH, et al. Among authors: bellissimo db. Blood. 2015 Apr 2;125(14):2297-304. doi: 10.1182/blood-2014-11-610824. Epub 2015 Feb 6. Blood. 2015. PMID: 25662333 Free PMC article.

7

Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States.

Flood VH, Christopherson PA, Gill JC, Friedman KD, Haberichter SL, Bellissimo DB, Udani RA, Dasgupta M, Hoffmann RG, Ragni MV, Shapiro AD, Lusher JM, Lentz SR, Abshire TC, Leissinger C, Hoots WK, Manco-Johnson MJ, Gruppo RA, Boggio LN, Montgomery KT, Goodeve AC, James PD, Lillicrap D, Peake IR, Montgomery RR. Flood VH, et al. Among authors: bellissimo db. Blood. 2016 May 19;127(20):2481-8. doi: 10.1182/blood-2015-10-673681. Epub 2016 Feb 9. Blood. 2016. PMID: 26862110 Free PMC article.

8

Common VWF sequence variants associated with higher VWF and FVIII are less frequent in subjects diagnosed with type 1 VWD.

Flood VH, Johnsen JM, Kochelek C, Slobodianuk TL, Christopherson PA, Haberichter SL, Udani R, Bellissimo DB, Friedman KD, Montgomery RR. Flood VH, et al. Among authors: bellissimo db. Res Pract Thromb Haemost. 2018 Jan 23;2(2):390-398. doi: 10.1002/rth2.12077. eCollection 2018 Apr. Res Pract Thromb Haemost. 2018. PMID: 30046743 Free PMC article.

9

Molecular pathogenesis and heterogeneity in type 3 VWD families in U.S. Zimmerman program.

Christopherson PA, Haberichter SL, Flood VH, Perry CL, Sadler BE, Bellissimo DB, Di Paola J, Montgomery RR; Zimmerman Program Investigators. Christopherson PA, et al. Among authors: bellissimo db. J Thromb Haemost. 2022 Jul;20(7):1576-1588. doi: 10.1111/jth.15713. Epub 2022 Apr 6. J Thromb Haemost. 2022. PMID: 35343054 Free article.

10

Prenatal Genotyping of the RhD Locus to Identify Fetuses at Risk for Hemolytic Disease of the Newborn.

Hessner MJ, Bellissimo DB. Hessner MJ, et al. Among authors: bellissimo db. Methods Mol Med. 2001;49:427-37. doi: 10.1385/1-59259-081-0:427. Methods Mol Med. 2001. PMID: 21370158

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