Brown SA - Search Results

1

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

2

Survival of von Willebrand factor released following DDAVP in a type 1 von Willebrand disease cohort: influence of glycosylation, proteolysis and gene mutations.

Millar CM, Riddell AF, Brown SA, Starke R, Mackie I, Bowen DJ, Jenkins PV, van Mourik JA. Millar CM, et al. Among authors: brown sa. Thromb Haemost. 2008 May;99(5):916-24. doi: 10.1160/TH07-09-0565. Thromb Haemost. 2008. PMID: 18449422 Clinical Trial.

3

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

4

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.

5

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

6

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

7

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.

8

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.

9

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. 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.

10

Oral anticoagulants and fetal loss.

Brown SA, Collins PW. Brown SA, et al. Lancet. 1996 Dec 21-28;348(9043):1734. doi: 10.1016/s0140-6736(05)65856-4. Lancet. 1996. PMID: 8973446 No abstract available.

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