Chalmers EA - Search Results

1

Management of neonates with inherited bleeding disorders--a survey of current UK practice.

Chalmers EA, Williams MD, Richards M, Brown SA, Liesner R, Thomas A, Vidler V, Pasi KJ, Hill FG; Paediatric Working Party of Ukhcdo. Chalmers EA, et al. Haemophilia. 2005 Mar;11(2):186-7. doi: 10.1111/j.1365-2516.2005.01072.x. Haemophilia. 2005. PMID: 15810924 No abstract available.

2

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. Haemophilia. 2007 Mar;13(2):149-55. doi: 10.1111/j.1365-2516.2006.01418.x. Haemophilia. 2007. PMID: 17286767

3

Treatment related factors and inhibitor development in children with severe haemophilia A.

Maclean PS, Richards M, Williams M, Collins P, Liesner R, Keeling DM, Yee T, Will AM, Young D, Chalmers EA; Paediatric Working Party of UKHCDO. Maclean PS, et al. Among authors: chalmers ea. Haemophilia. 2011 Mar;17(2):282-7. doi: 10.1111/j.1365-2516.2010.02422.x. Epub 2010 Nov 11. Haemophilia. 2011. PMID: 21070501

4

The use of enhanced half-life coagulation factor concentrates in routine clinical practice: guidance from UKHCDO.

Collins P, Chalmers E, Chowdary P, Keeling D, Mathias M, O'Donnell J, Pasi KJ, Rangarajan S, Thomas A. Collins P, et al. Haemophilia. 2016 Jul;22(4):487-98. doi: 10.1111/hae.13013. Epub 2016 Jun 16. Haemophilia. 2016. PMID: 27311929 Review.

5

First-line immune tolerance induction for children with severe haemophilia A: A protocol from the UK Haemophilia Centre Doctors' Organisation Inhibitor and Paediatric Working Parties.

Collins P, Chalmers E, Alamelu J, Hay C, Liesner R, Makris M, Mathias M, Payne J, Rangarajan S, Richards M, Talks K, Tunstall O, Williams M, Hart DP. Collins P, et al. Haemophilia. 2017 Sep;23(5):654-659. doi: 10.1111/hae.13264. Epub 2017 Jun 2. Haemophilia. 2017. PMID: 28574205 No abstract available.

6

The incidence of factor VIII inhibitors in severe haemophilia A following a major switch from full-length to B-domain-deleted factor VIII: a prospective cohort comparison.

Hay CRM, Palmer BP, Chalmers EA, Hart DP, Liesner R, Rangarajan S, Talks K, Williams M, Collins PW. Hay CRM, et al. Among authors: chalmers ea. Haemophilia. 2015 Mar;21(2):219-226. doi: 10.1111/hae.12563. Epub 2014 Nov 7. Haemophilia. 2015. PMID: 25382829

7

A national survey of immunosuppression strategies for acquired haemophilia A.

Batty P, Palmer B, Chalmers E, Hay CR, Liesner R, Rangarajan S, Talks K, Williams M, Collins P, Hart DP. Batty P, et al. Haemophilia. 2015 Jan;21(1):e73-6. doi: 10.1111/hae.12547. Epub 2014 Nov 24. Haemophilia. 2015. PMID: 25422109 No abstract available.

8

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: chalmers ea. Haemophilia. 2004 Sep;10(5):593-628. doi: 10.1111/j.1365-2516.2004.00944.x. Haemophilia. 2004. PMID: 15357789 Review.

9

Haemophilia care in central Scotland 1980-94. I. Demographic characteristics, hospital admissions and causes of death.

Ludlam CA, Lee RJ, Prescott RJ, Andrews J, Kirke E, Thomas AE, Chalmers E, Lowe GD. Ludlam CA, et al. Haemophilia. 2000 Sep;6(5):494-503. doi: 10.1046/j.1365-2516.2000.00405.x. Haemophilia. 2000. PMID: 11012692

10

Long-term follow-up of neonatal intracranial haemorrhage in children with severe haemophilia.

Andersson NG, Wu R, Carcao M, Claeyssens-Donadel S, Kobelt R, Liesner R, Mäkipernaa A, Ranta S, Ljung R; ICH study group. Andersson NG, et al. Br J Haematol. 2020 Jul;190(2):e101-e104. doi: 10.1111/bjh.16740. Epub 2020 Jun 9. Br J Haematol. 2020. PMID: 32519345 Free article. No abstract available.

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