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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1984 1
1991 1
1994 1
1995 2
1996 1
1997 1
2000 1
2001 1
2005 2
2006 2
2007 1
2008 2
2009 1
2010 1
2011 2
2012 2
2015 1
2016 2
2018 1
2019 1
2022 1
2023 1
2024 0

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28 results

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Page 1
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.
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.
Curated disease-causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTH.
Megy K, Downes K, Simeoni I, Bury L, Morales J, Mapeta R, Bellissimo DB, Bray PF, Goodeve AC, Gresele P, Lambert M, Reitsma P, Ouwehand WH, Freson K; Subcommittee on Genomics in Thrombosis and Hemostasis. Megy K, et al. Among authors: bellissimo db. J Thromb Haemost. 2019 Aug;17(8):1253-1260. doi: 10.1111/jth.14479. Epub 2019 Jun 9. J Thromb Haemost. 2019. PMID: 31179617 Free PMC article. No abstract available.
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.
Simeoni I, Stephens JC, Hu F, Deevi SV, Megy K, Bariana TK, Lentaigne C, Schulman S, Sivapalaratnam S, Vries MJ, Westbury SK, Greene D, Papadia S, Alessi MC, Attwood AP, Ballmaier M, Baynam G, Bermejo E, Bertoli M, Bray PF, Bury L, Cattaneo M, Collins P, Daugherty LC, Favier R, French DL, Furie B, Gattens M, Germeshausen M, Ghevaert C, Goodeve AC, Guerrero JA, Hampshire DJ, Hart DP, Heemskerk JW, Henskens YM, Hill M, Hogg N, Jolley JD, Kahr WH, Kelly AM, Kerr R, Kostadima M, Kunishima S, Lambert MP, Liesner R, López JA, Mapeta RP, Mathias M, Millar CM, Nathwani A, Neerman-Arbez M, Nurden AT, Nurden P, Othman M, Peerlinck K, Perry DJ, Poudel P, Reitsma P, Rondina MT, Smethurst PA, Stevenson W, Szkotak A, Tuna S, van Geet C, Whitehorn D, Wilcox DA, Zhang B, Revel-Vilk S, Gresele P, Bellissimo DB, Penkett CJ, Laffan MA, Mumford AD, Rendon A, Gomez K, Freson K, Ouwehand WH, Turro E. Simeoni I, et al. Among authors: bellissimo db. Blood. 2016 Jun 9;127(23):2791-803. doi: 10.1182/blood-2015-12-688267. Epub 2016 Apr 15. Blood. 2016. PMID: 27084890 Free PMC article.
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.
Characterization of copy-number variants in a large cohort of patients with von Willebrand disease reveals a relationship between disrupted regions and disease type.
Sadler B, Christopherson PA, Perry CL, Bellissimo DB, Haberichter SL, Haller G, Antunes L, Flood VH, Di Paola J, Montgomery RR; Zimmerman Program Investigators. Sadler B, et al. Among authors: bellissimo db. Res Pract Thromb Haemost. 2023 Oct 14;7(7):102232. doi: 10.1016/j.rpth.2023.102232. eCollection 2023 Oct. Res Pract Thromb Haemost. 2023. PMID: 38077814 Free PMC article.
Molecular cloning of human liver sulfite oxidase.
Garrett RM, Bellissimo DB, Rajagopalan KV. Garrett RM, et al. Among authors: bellissimo db. Biochim Biophys Acta. 1995 Jun 9;1262(2-3):147-9. doi: 10.1016/0167-4781(95)00068-r. Biochim Biophys Acta. 1995. PMID: 7599189
28 results