Brown S - Search Results

1

The diagnosis and management of factor VIII and IX inhibitors: a guideline from the United Kingdom Haemophilia Centre Doctors Organisation.

Hay CR, Brown S, Collins PW, Keeling DM, Liesner R. Hay CR, et al. Among authors: brown s. Br J Haematol. 2006 Jun;133(6):591-605. doi: 10.1111/j.1365-2141.2006.06087.x. Br J Haematol. 2006. PMID: 16704433 Free article. Review.

2

Acquired hemophilia A in the United Kingdom: a 2-year national surveillance study by the United Kingdom Haemophilia Centre Doctors' Organisation.

Collins PW, Hirsch S, Baglin TP, Dolan G, Hanley J, Makris M, Keeling DM, Liesner R, Brown SA, Hay CR; UK Haemophilia Centre Doctors' Organisation. Collins PW, et al. Among authors: brown sa. Blood. 2007 Mar 1;109(5):1870-7. doi: 10.1182/blood-2006-06-029850. Epub 2006 Oct 17. Blood. 2007. PMID: 17047148 Free article.

3

The diagnosis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization.

Laffan M, Brown SA, Collins PW, Cumming AM, Hill FG, Keeling D, Peake IR, Pasi KJ. Laffan M, et al. Among authors: brown sa. Haemophilia. 2004 May;10(3):199-217. doi: 10.1111/j.1365-2516.2004.00894.x. Haemophilia. 2004. PMID: 15086318

4

Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization.

Pasi KJ, Collins PW, Keeling DM, Brown SA, Cumming AM, Dolan GC, Hay CR, Hill FG, Laffan M, Peake IR. Pasi KJ, et al. Among authors: brown sa. Haemophilia. 2004 May;10(3):218-31. doi: 10.1111/j.1365-2516.2004.00886.x. Haemophilia. 2004. PMID: 15086319

5

Early factor VIII exposure and subsequent inhibitor development in children with severe haemophilia A.

Chalmers EA, Brown SA, Keeling D, Liesner R, Richards M, Stirling D, Thomas A, Vidler V, Williams MD, Young D; Paediatric Working Party of UKHCDO. Chalmers EA, et al. Among authors: brown sa. Haemophilia. 2007 Mar;13(2):149-55. doi: 10.1111/j.1365-2516.2006.01418.x. Haemophilia. 2007. PMID: 17286767

6

Long-term follow up of patients treated with intermediate FVIII concentrate BPL 8Y.

Brown SA, Dasani H, Collins PW. Brown SA, et al. Haemophilia. 1998 Mar;4(2):89-93. doi: 10.1046/j.1365-2516.1998.00153.x. Haemophilia. 1998. PMID: 9873844 Clinical Trial.

7

Long-term safety and efficacy of recombinant factor VIII Fc fusion protein (rFVIIIFc) in subjects with haemophilia A.

Nolan B, Mahlangu J, Perry D, Young G, Liesner R, Konkle B, Rangarajan S, Brown S, Hanabusa H, Pasi KJ, Pabinger I, Jackson S, Cristiano LM, Li X, Pierce GF, Allen G. Nolan B, et al. Among authors: brown s. Haemophilia. 2016 Jan;22(1):72-80. doi: 10.1111/hae.12766. Epub 2015 Jul 27. Haemophilia. 2016. PMID: 26218032 Clinical Trial.

8

Increased clearance of von Willebrand factor antigen post-DDAVP in Type 1 von Willebrand disease: is it a potential pathogenic process?

Brown SA, Eldridge A, Collins PW, Bowen DJ. Brown SA, et al. J Thromb Haemost. 2003 Aug;1(8):1714-7. doi: 10.1046/j.1538-7836.2003.00359.x. J Thromb Haemost. 2003. PMID: 12911582 Free article.

9

Heterogeneous detection of A-antigen on von Willebrand factor derived from platelets, endothelial cells and plasma.

Brown SA, Collins PW, Bowen DJ. Brown SA, et al. Thromb Haemost. 2002 Jun;87(6):990-6. Thromb Haemost. 2002. PMID: 12083507

10

Factor VIIa induced release of von Willebrand factor from human umbilical vein endothelial cells by a tyrosine kinase dependent pathway.

Brown SA, Bowen DJ, Hallett MB, Giddings JC, Collins PW. Brown SA, et al. Thromb Haemost. 2002 Jun;87(6):1057-61. Thromb Haemost. 2002. PMID: 12083486

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