"von Willebrand Disease, Type 3"[mh] - Search Results

Year	Number of Results
2008	1
2009	3
2010	9
2011	10
2012	10
2013	14
2014	7
2015	4
2016	9
2017	4
2018	6
2019	11
2020	6
2021	11
2022	13
2023	8
2024	8
2025	1

1

Type 3 von Willebrand Disease in Pregnancy: A Systematic Literature Review.

Makhamreh MM, Kass SL, Russo ML, Ahmadzia H, Al-Kouatly HB. Makhamreh MM, et al. Am J Perinatol. 2021 Apr;38(5):436-448. doi: 10.1055/s-0039-1700541. Epub 2019 Nov 22. Am J Perinatol. 2021. PMID: 31756759

2

Diagnosis and treatment of von Willebrand disease in 2024 and beyond.

James P, Leebeek F, Casari C, Lillicrap D. James P, et al. Haemophilia. 2024 Apr;30 Suppl 3:103-111. doi: 10.1111/hae.14970. Epub 2024 Mar 13. Haemophilia. 2024. PMID: 38481079 Review.

3

Prophylaxis with recombinant von Willebrand factor in patients with type 3 von Willebrand disease: Results of a post hoc analysis from a phase 3 trial.

Leebeek FWG, Peyvandi F, Tiede A, Castaman G, Escobar M, Wang M, Zülfikar B, Susen S, Miesbach W, Wang S, Wang Y, Zhang J, Özen G. Leebeek FWG, et al. Eur J Haematol. 2023 Jul;111(1):29-40. doi: 10.1111/ejh.13949. Epub 2023 Apr 11. Eur J Haematol. 2023. PMID: 36823994 Free article. Clinical Trial.

4

An evaluation of von Willebrand factor (recombinant) therapy for adult patients living with severe type 3 von Willebrand disease.

Hancock JM, Escobar MA. Hancock JM, et al. Expert Rev Hematol. 2023 Mar;16(3):157-161. doi: 10.1080/17474086.2023.2184339. Epub 2023 Mar 2. Expert Rev Hematol. 2023. PMID: 36861346 Review.

5

Type-3 von Willebrand disease in India-Clinical spectrum and molecular profile.

Elayaperumal S, Fouzia NA, Biswas A, Nair SC, Viswabandya A, George B, Abraham A, Oldenburg J, Edison ES, Srivastava A. Elayaperumal S, et al. Haemophilia. 2018 Nov;24(6):930-940. doi: 10.1111/hae.13542. Epub 2018 Jul 8. Haemophilia. 2018. PMID: 29984440

6

von Willebrand factor neutralizing and non-neutralizing alloantibodies in 213 subjects with type 3 von Willebrand disease enrolled in 3WINTERS-IPS.

Pagliari MT, Budde U, Baronciani L, Eshghi P, Ahmadinejad M, Badiee Z, Baghaipour MR, Benítez Hidalgo O, Biguzzi E, Bodó I, Castaman G, Goudemand J, Karimi M, Keikhaei B, Lassila R, Leebeek FWG, Lopez Fernandez MF, Marino R, Oldenburg J, Peake I, Santoro C, Schneppenheim R, Tiede A, Toogeh G, Tosetto A, Trossaert M, Yadegari H, Zetterberg EMK, Mannucci PM, Federici AB, Eikenboom J, Peyvandi F. Pagliari MT, et al. J Thromb Haemost. 2023 Apr;21(4):787-799. doi: 10.1016/j.jtha.2023.01.001. Epub 2023 Jan 11. J Thromb Haemost. 2023. PMID: 36792472 Free article.

7

Platelets compensate for poor thrombin generation in type 3 von Willebrand disease.

Szanto T, Nummi V, Jouppila A, Brinkman HJM, Lassila R. Szanto T, et al. Platelets. 2020;31(1):103-111. doi: 10.1080/09537104.2019.1581922. Epub 2019 Mar 5. Platelets. 2020. PMID: 30836803 Free article.

8

Laboratory characterization of obligate carriers of type 3 von Willebrand disease with a potential role for Platelet Function Analyzer (PFA-200).

Geevar T, Dave RG, Mathews NS, Kumar S, Mammen JJ, Vijayan R, Aboobacker FN, Abraham A, Srivastava A, Nair SC. Geevar T, et al. Int J Lab Hematol. 2022 Jun;44(3):603-609. doi: 10.1111/ijlh.13787. Epub 2022 Jan 5. Int J Lab Hematol. 2022. PMID: 34986515

9

Variants p.Pro2063Ser and p.Arg324* co-segregate in type 3 von Willebrand disease patients from Southern Brazil.

Ornaghi AP, Meireles MR, Botton MR, Salzano FM, Bandinelli E, Matte U. Ornaghi AP, et al. Haemophilia. 2021 Mar;27(2):e204-e213. doi: 10.1111/hae.14254. Epub 2021 Feb 6. Haemophilia. 2021. PMID: 33550700

10

Von Willebrand Disease: Gaining a global perspective.

O'Sullivan JM, Tootoonchian E, Ziemele B, Makris M, Federici AB, Khayat Djambas C, El Ekiaby M, Rotellini D, Sidonio RF, Iorio A, Coffin D, Pierce GF, Stonebraker J, James PD, Lavin M. O'Sullivan JM, et al. Haemophilia. 2023 Jul;29(4):1104-1112. doi: 10.1111/hae.14804. Epub 2023 May 22. Haemophilia. 2023. PMID: 37216656

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