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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 3 |
2012 | 3 |
2018 | 1 |
2024 | 0 |
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Page 1
Exploring the biological basis of haemophilic joint disease: experimental studies.
Haemophilia. 2012 May;18(3):310-8. doi: 10.1111/j.1365-2516.2011.02669.x. Epub 2011 Nov 2.
Haemophilia. 2012.
PMID: 22044636
Review.
The international factor IX treatment network survey.
Berntorp E, Shapiro AD, Waters J, Astermark J; International Factor IX Treatment Network.
Berntorp E, et al.
Haemophilia. 2012 May;18(3):e60-2. doi: 10.1111/j.1365-2516.2012.02767.x. Epub 2012 Mar 8.
Haemophilia. 2012.
PMID: 22404549
No abstract available.
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The quinoxaline anti-tumor agent (R+)XK469 inhibits neuroblastoma tumor growth.
Kakodkar NC, Peddinti R, Kletzel M, Tian Y, Guerrero LJ, Undevia SD, Geary D, Chlenski A, Yang Q, Salwen HR, Cohn SL.
Kakodkar NC, et al.
Pediatr Blood Cancer. 2011 Jan;56(1):164-7. doi: 10.1002/pbc.22639.
Pediatr Blood Cancer. 2011.
PMID: 20860039
Free PMC article.
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Sorafenib inhibits neuroblastoma cell proliferation and signaling, blocks angiogenesis, and impairs tumor growth.
Kakodkar NC, Peddinti RR, Tian Y, Guerrero LJ, Chlenski A, Yang Q, Salwen HR, Maitland ML, Cohn SL.
Kakodkar NC, et al.
Pediatr Blood Cancer. 2012 Oct;59(4):642-7. doi: 10.1002/pbc.24004. Epub 2011 Dec 6.
Pediatr Blood Cancer. 2012.
PMID: 22147414
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Phase 1, single-dose escalating study of marzeptacog alfa (activated), a recombinant factor VIIa variant, in patients with severe hemophilia.
Gruppo RA, Malan D, Kapocsi J, Nemes L, Hay CRM, Boggio L, Chowdary P, Tagariello G, von Drygalski A, Hua F, Scaramozza M, Arkin S; Marzeptacog alfa (activated) Study Group Investigators.
Gruppo RA, et al.
J Thromb Haemost. 2018 Oct;16(10):1984-1993. doi: 10.1111/jth.14247. Epub 2018 Aug 27.
J Thromb Haemost. 2018.
PMID: 30151972
Free article.
Clinical Trial.
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