Kavakli K - Search Results

1

Phase 3 study of recombinant von Willebrand factor in patients with severe von Willebrand disease who are undergoing elective surgery.

Peyvandi F, Mamaev A, Wang JD, Stasyshyn O, Timofeeva M, Curry N, Cid AR, Yee TT, Kavakli K, Castaman G, Sytkowski A. Peyvandi F, et al. Among authors: kavakli k. J Thromb Haemost. 2019 Jan;17(1):52-62. doi: 10.1111/jth.14313. Epub 2018 Dec 20. J Thromb Haemost. 2019. PMID: 30362288 Free PMC article. Clinical Trial.

2

Intraleucocyte platelet-activating factor levels in desmopressin-treated patients with haemophilia A and von Willebrand disease.

Kavakli K, Hüseyinov A, Coker I, Aydinok Y, Nisli G. Kavakli K, et al. Haemophilia. 2001 Sep;7(5):482-9. doi: 10.1046/j.1365-2516.2001.00535.x. Haemophilia. 2001. PMID: 11554936

3

Frequency of acquired von Willebrand's disease in children with congenital heart disease.

Arslan MT, Ozyurek R, Kavakli K, Levent E, Ulger Z, Gurses D, Akyol B, Atay Y. Arslan MT, et al. Among authors: kavakli k. Acta Cardiol. 2007 Aug;62(4):403-8. doi: 10.2143/AC.62.4.2022285. Acta Cardiol. 2007. PMID: 17824302

4

Surgery in patients with haemophilia and high responding inhibitors: Izmir experience.

Balkan C, Karapinar D, Aydogdu S, Ozcan C, Ay Y, Akin M, Kavakli K. Balkan C, et al. Among authors: kavakli k. Haemophilia. 2010 Nov;16(6):902-9. doi: 10.1111/j.1365-2516.2010.02329.x. Haemophilia. 2010. PMID: 20518817

5

Resemblance to vWD types and laboratory diagnosis of obligatory carriers of type 3 von Willebrand disease.

Akin M, Karapinar DY, Balkan C, Ay Y, Kavakli K. Akin M, et al. Among authors: kavakli k. Clin Appl Thromb Hemost. 2011 Nov-Dec;17(6):E21-4. doi: 10.1177/1076029610379847. Epub 2010 Aug 16. Clin Appl Thromb Hemost. 2011. PMID: 20713487 Free article.

6

The influence of the ABO blood type on the distribution of von Willebrand factor in healthy children with no bleeding symptoms.

Akin M, Balkan C, Karapinar DY, Kavakli K. Akin M, et al. Among authors: kavakli k. Clin Appl Thromb Hemost. 2012 Jun;18(3):316-9. doi: 10.1177/1076029611422364. Epub 2011 Sep 23. Clin Appl Thromb Hemost. 2012. PMID: 21949039 Free article. Clinical Trial.

7

Laboratory diagnosis and management of von Willebrand disease in Turkey: Izmir experience.

Akin M, Kavakli K. Akin M, et al. Among authors: kavakli k. Semin Thromb Hemost. 2011 Jul;37(5):581-6. doi: 10.1055/s-0031-1281046. Epub 2011 Nov 18. Semin Thromb Hemost. 2011. PMID: 22102203 Review.

8

Recombinant factor VIIa analog (vatreptacog alfa [activated]) for treatment of joint bleeds in hemophilia patients with inhibitors: a randomized controlled trial.

de Paula EV, Kavakli K, Mahlangu J, Ayob Y, Lentz SR, Morfini M, Nemes L, Šalek SZ, Shima M, Windyga J, Ehrenforth S, Chuansumrit A; 1804 (adept(TM)1) Investigators. de Paula EV, et al. Among authors: kavakli k. J Thromb Haemost. 2012 Jan;10(1):81-9. doi: 10.1111/j.1538-7836.2011.04549.x. J Thromb Haemost. 2012. PMID: 22470921 Free article. Clinical Trial.

9

Prophylaxis in severe forms of von Willebrand's disease: results from the von Willebrand Disease Prophylaxis Network (VWD PN).

Abshire TC, Federici AB, Alvárez MT, Bowen J, Carcao MD, Cox Gill J, Key NS, Kouides PA, Kurnik K, Lail AE, Leebeek FW, Makris M, Mannucci PM, Winikoff R, Berntorp E; VWD PN. Abshire TC, et al. Haemophilia. 2013 Jan;19(1):76-81. doi: 10.1111/j.1365-2516.2012.02916.x. Epub 2012 Jul 23. Haemophilia. 2013. PMID: 22823000 Free PMC article.

10

Recombinant factor VIIa analog in the management of hemophilia with inhibitors: results from a multicenter, randomized, controlled trial of vatreptacog alfa.

Lentz SR, Ehrenforth S, Karim FA, Matsushita T, Weldingh KN, Windyga J, Mahlangu JN; adept™2 investigators. Lentz SR, et al. J Thromb Haemost. 2014 Aug;12(8):1244-53. doi: 10.1111/jth.12634. Epub 2014 Jul 16. J Thromb Haemost. 2014. PMID: 24931322 Free PMC article. Clinical Trial.

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