Hill FG - Search Results

1

Recommendations for the treatment of factor VIII inhibitors: from the UK Haemophilia Centre Directors' Organisation Inhibitor Working Party.

Hay CR, Colvin BT, Ludlam CA, Hill FG, Preston FE. Hay CR, et al. Among authors: hill fg. Blood Coagul Fibrinolysis. 1996 Mar;7(2):134-8. Blood Coagul Fibrinolysis. 1996. PMID: 8735802

2

The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977-99.

Darby SC, Keeling DM, Spooner RJ, Wan Kan S, Giangrande PL, Collins PW, Hill FG, Hay CR; UK Haemophilia Centre Doctors' Organisation. Darby SC, et al. Among authors: hill fg. J Thromb Haemost. 2004 Jul;2(7):1047-54. doi: 10.1046/j.1538-7836.2004.00710.x. J Thromb Haemost. 2004. PMID: 15219185 Free article.

3

Factor VIII inhibitors in mild and moderate-severity haemophilia A. UK Haemophilia Centre Directors Organisation.

Hay CR, Ludlam CA, Colvin BT, Hill FG, Preston FE, Wasseem N, Bagnall R, Peake IR, Berntorp E, Mauser Bunschoten EP, Fijnvandraat K, Kasper CK, White G, Santagostino E. Hay CR, et al. Among authors: hill fg. Thromb Haemost. 1998 Apr;79(4):762-6. Thromb Haemost. 1998. PMID: 9569189

4

The diagnosis and management of factor VIII and IX inhibitors: a guideline from the UK Haemophilia Centre Doctors' Organization (UKHCDO).

Hay CR, Baglin TP, Collins PW, Hill FG, Keeling DM. Hay CR, et al. Among authors: hill fg. Br J Haematol. 2000 Oct;111(1):78-90. doi: 10.1046/j.1365-2141.2000.02327.x. Br J Haematol. 2000. PMID: 11091185 Free article. No abstract available.

5

The incidence of factor VIII inhibitors in the United Kingdom, 1990-93. Inhibitor Working Party. United Kingdom Haemophilia Centre Directors Organization.

Colvin BT, Hay CR, Hill FG, Preston FE. Colvin BT, et al. Among authors: hill fg. Br J Haematol. 1995 Apr;89(4):908-10. doi: 10.1111/j.1365-2141.1995.tb08435.x. Br J Haematol. 1995. PMID: 7772532

6

HLA class II profile: a weak determinant of factor VIII inhibitor development in severe haemophilia A. UKHCDO Inhibitor Working Party.

Hay CR, Ollier W, Pepper L, Cumming A, Keeney S, Goodeve AC, Colvin BT, Hill FG, Preston FE, Peake IR. Hay CR, et al. Among authors: hill fg. Thromb Haemost. 1997 Feb;77(2):234-7. Thromb Haemost. 1997. PMID: 9157572

7

Mortality rates, life expectancy, and causes of death in people with hemophilia A or B in the United Kingdom who were not infected with HIV.

Darby SC, Kan SW, Spooner RJ, Giangrande PL, Hill FG, Hay CR, Lee CA, Ludlam CA, Williams M. Darby SC, et al. Among authors: hill fg. Blood. 2007 Aug 1;110(3):815-25. doi: 10.1182/blood-2006-10-050435. Epub 2007 Apr 19. Blood. 2007. PMID: 17446349 Free article.

8

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: hill fg. Haemophilia. 2004 May;10(3):218-31. doi: 10.1111/j.1365-2516.2004.00886.x. Haemophilia. 2004. PMID: 15086319

9

A framework for genetic service provision for haemophilia and other inherited bleeding disorders.

Ludlam CA, Pasi KJ, Bolton-Maggs P, Collins PW, Cumming AM, Dolan G, Fryer A, Harrington C, Hill FG, Peake IR, Perry DJ, Skirton H, Smith M; UK Haemophilia Centre Doctors' Organisation. Ludlam CA, et al. Among authors: hill fg. Haemophilia. 2005 Mar;11(2):145-63. doi: 10.1111/j.1365-2516.2005.01070.x. Haemophilia. 2005. PMID: 15810917

10

An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type 1 von Willebrand disease.

Cumming A, Grundy P, Keeney S, Lester W, Enayat S, Guilliatt A, Bowen D, Pasi J, Keeling D, Hill F, Bolton-Maggs PH, Hay C, Collins P; UK Haemophilia Centre Doctors' Organisation. Cumming A, et al. Thromb Haemost. 2006 Nov;96(5):630-41. Thromb Haemost. 2006. PMID: 17080221

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