Wilde J - Search Results

1

FEIBA prophylaxis in haemophilia patients: a clinical update and treatment recommendations.

Perry D, Berntorp E, Tait C, Dolan G, Holme PA, Laffan M, Lassila R, Mumford A, Pasi J, Wilde J, Will A, Yee TT. Perry D, et al. Among authors: wilde j. Haemophilia. 2010 Jan;16(1):80-9. doi: 10.1111/j.1365-2516.2009.02104.x. Epub 2009 Sep 23. Haemophilia. 2010. PMID: 19780845

2

Experience of four UK comprehensive care centres using FEIBA® for surgeries in patients with inhibitors.

Rangarajan S, Yee TT, Wilde J. Rangarajan S, et al. Among authors: wilde j. Haemophilia. 2011 Jan;17(1):28-34. doi: 10.1111/j.1365-2516.2010.02360.x. Haemophilia. 2011. PMID: 20642787

3

The rare coagulation disorders--review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation.

Bolton-Maggs PH, Perry DJ, Chalmers EA, Parapia LA, Wilde JT, Williams MD, Collins PW, Kitchen S, Dolan G, Mumford AD. Bolton-Maggs PH, et al. Among authors: wilde jt. Haemophilia. 2004 Sep;10(5):593-628. doi: 10.1111/j.1365-2516.2004.00944.x. Haemophilia. 2004. PMID: 15357789 Review.

4

UKHCDO guidelines on the management of HCV in patients with hereditary bleeding disorders 2011.

Wilde JT, Mutimer D, Dolan G, Millar C, Watson HG, Yee TT, Makris M. Wilde JT, et al. Haemophilia. 2011 Sep;17(5):e877-83. doi: 10.1111/j.1365-2516.2011.02585.x. Epub 2011 Jun 9. Haemophilia. 2011. PMID: 21658165 Review.

5

Risk reduction strategies for variant Creutzfeldt-Jakob disease transmission by UK plasma products and their impact on patients with inherited bleeding disorders.

Millar CM, Connor N, Dolan G, Lee CA, Makris M, Wilde J, Winter M, Ironside JW, Gill N, Hill FG. Millar CM, et al. Among authors: wilde j. Haemophilia. 2010 Mar;16(2):305-15. doi: 10.1111/j.1365-2516.2010.02220.x. Haemophilia. 2010. PMID: 20487442

6

Consensus protocol for the use of recombinant activated factor VII [eptacog alfa (activated); NovoSeven] in elective orthopaedic surgery in haemophilic patients with inhibitors.

Giangrande PL, Wilde JT, Madan B, Ludlam CA, Tuddenham EG, Goddard NJ, Dolan G, Ingerslev J. Giangrande PL, et al. Among authors: wilde jt. Haemophilia. 2009 Mar;15(2):501-8. doi: 10.1111/j.1365-2516.2008.01952.x. Epub 2009 Feb 1. Haemophilia. 2009. PMID: 19187194

7

Update to UKHCDO guidance on vaccination against hepatitis A and B viruses in patients with inherited coagulation factor deficiencies and von Willebrand disease.

Watson HG, Wilde JT, Dolan G, Millar C, Yee TT, Makris M; Morbidity and Mortality Working Party UKHCDO. Watson HG, et al. Among authors: wilde jt. Haemophilia. 2013 May;19(3):e191-2. doi: 10.1111/hae.12139. Haemophilia. 2013. PMID: 23600911 No abstract available.

8

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.

9

The risk of variant Creutzfeldt-Jakob disease among UK patients with bleeding disorders, known to have received potentially contaminated plasma products.

Zaman SM, Hill FG, Palmer B, Millar CM, Bone A, Molesworth AM, Connor N, Lee CA, Dolan G, Wilde JT, Gill ON, Makris M. Zaman SM, et al. Among authors: wilde jt. Haemophilia. 2011 Nov;17(6):931-7. doi: 10.1111/j.1365-2516.2011.02508.x. Epub 2011 Feb 23. Haemophilia. 2011. PMID: 21342369

10

Haemophilia 2002: emerging risks of treatment.

Evatt BL, Farrugia A, Shapiro AD, Wilde JT. Evatt BL, et al. Among authors: wilde jt. Haemophilia. 2002 May;8(3):221-9. doi: 10.1046/j.1365-2516.2002.00612.x. Haemophilia. 2002. PMID: 12010415 Review.

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