Pasi KJ - Search Results

1

Clinical experience of factor XI deficiency: the role of fresh frozen plasma and factor XI concentrate.

Collins PW, Goldman E, Lilley P, Pasi KJ, Lee CA. Collins PW, et al. Among authors: pasi kj. Haemophilia. 1995 Oct;1(4):227-31. doi: 10.1111/j.1365-2516.1995.tb00080.x. Haemophilia. 1995. PMID: 27214628

2

Successful long-term treatment with porcine factor VIII of a patient with haemophilia A and an inhibitor to factor VIII.

Vyas P, Pasi KJ, Lee CA. Vyas P, et al. Among authors: pasi kj. Haemophilia. 1996 Oct;2(4):240-3. doi: 10.1111/j.1365-2516.1996.tb00144.x. Haemophilia. 1996. PMID: 27214364 No abstract available.

3

Analysis of intron 22 inversions of the factor VIII gene in severe hemophilia A: implications for genetic counseling.

Jenkins PV, Collins PW, Goldman E, McCraw A, Riddell A, Lee CA, Pasi KJ. Jenkins PV, et al. Among authors: pasi kj. Blood. 1994 Oct 1;84(7):2197-201. Blood. 1994. PMID: 7919335 Free article.

4

Comparison of immunodeficiency and AIDS defining conditions in HIV negative and HIV positive men with haemophilia A.

Sabin CA, Pasi KJ, Phillips AN, Lilley P, Bofill M, Lee CA. Sabin CA, et al. Among authors: pasi kj. BMJ. 1996 Jan 27;312(7025):207-10. doi: 10.1136/bmj.312.7025.207. BMJ. 1996. PMID: 8563582 Free PMC article.

5

Transmission of symptomatic parvovirus B19 infection by clotting factor concentrate.

Yee TT, Cohen BJ, Pasi KJ, Lee CA. Yee TT, et al. Among authors: pasi kj. Br J Haematol. 1996 May;93(2):457-9. doi: 10.1046/j.1365-2141.1996.5161062.x. Br J Haematol. 1996. PMID: 8639448

6

Recurrent venous thromboembolic disease and factor XI concentrate in a patient with severe factor XI deficiency, chronic myelomonocytic leukaemia, factor V Leiden and heterozygous plasminogen deficiency.

Evans G, Pasi KJ, Mehta A, Lee CA, Perry DJ. Evans G, et al. Among authors: pasi kj. Blood Coagul Fibrinolysis. 1997 Oct;8(7):437-40. doi: 10.1097/00001721-199710000-00009. Blood Coagul Fibrinolysis. 1997. PMID: 9391725

7

Factor VIII inhibitors in haemophiliacs: a single-centre experience over 34 years, 1964-97.

Yee TT, Pasi KJ, Lilley PA, Lee CA. Yee TT, et al. Among authors: pasi kj. Br J Haematol. 1999 Mar;104(4):909-14. doi: 10.1046/j.1365-2141.1999.01268.x. Br J Haematol. 1999. PMID: 10192458 Free article.

8

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: pasi kj. Haemophilia. 2004 May;10(3):199-217. doi: 10.1111/j.1365-2516.2004.00894.x. Haemophilia. 2004. PMID: 15086318

9

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

10

Carrier detection and prenatal diagnosis by intron 22 inversion analysis of the factor VIII gene.

Ononye C, Jenkins PV, Goldman E, Pasi KJ. Ononye C, et al. Among authors: pasi kj. Haemophilia. 1995 Jul;1(3):204-6. doi: 10.1111/j.1365-2516.1995.tb00071.x. Haemophilia. 1995. PMID: 27214543

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