Mitchell M - Search Results

1

Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families.

Keskin EY, Gürsel T, Kaya Z, Dai L, Koçak Ü, Yenicesu İ, Belen FB, Mitchell M. Keskin EY, et al. Among authors: mitchell m. Blood Coagul Fibrinolysis. 2015 Jan;26(1):63-8. doi: 10.1097/MBC.0000000000000185. Blood Coagul Fibrinolysis. 2015. PMID: 25158988

2

Characterisation of five factor XI mutations.

Mitchell MJ, Dai L, Clarke JB, Bolton-Maggs PH, Savidge GF, Alhaq A. Mitchell MJ, et al. Thromb Haemost. 2007 Jun;97(6):884-9. doi: 10.1160/th06-12-0704. Thromb Haemost. 2007. PMID: 17549289

3

An Alu-mediated 31.5-kb deletion as the cause of factor XI deficiency in 2 unrelated patients.

Mitchell M, Dai L, Savidge G, Alhaq A. Mitchell M, et al. Blood. 2004 Oct 15;104(8):2394-6. doi: 10.1182/blood-2004-04-1318. Epub 2004 Jun 29. Blood. 2004. PMID: 15226185 Free article.

4

Three dominant-negative mutations in factor XI-deficient patients.

Dai L, Rangarajan S, Mitchell M. Dai L, et al. Among authors: mitchell m. Haemophilia. 2011 Sep;17(5):e919-22. doi: 10.1111/j.1365-2516.2011.02519.x. Epub 2011 Apr 3. Haemophilia. 2011. PMID: 21457405

5

Spectrum of factor XI (F11) mutations in the UK population--116 index cases and 140 mutations.

Mitchell M, Mountford R, Butler R, Alhaq A, Dai L, Savidge G, Bolton-Maggs PH. Mitchell M, et al. Hum Mutat. 2006 Aug;27(8):829. doi: 10.1002/humu.9439. Hum Mutat. 2006. PMID: 16835901

6

The profibrinolytic effect of plasma thrombomodulin in factor XI deficiency and its implications in hemostasis.

Dai L, Mitchell M, Savidge G, Alhaq A. Dai L, et al. Among authors: mitchell m. J Thromb Haemost. 2004 Dec;2(12):2200-4. doi: 10.1111/j.1538-7836.2004.01034.x. J Thromb Haemost. 2004. PMID: 15613027 Free article.

7

The significance of published polymorphisms in 14 cases of mild factor VII deficiency.

Cutler JA, Patel R, Mitchell MJ, Savidge GF. Cutler JA, et al. Blood Coagul Fibrinolysis. 2005 Mar;16(2):91-5. doi: 10.1097/01.mbc.0000161561.51517.31. Blood Coagul Fibrinolysis. 2005. PMID: 15741795

8

Genotype analysis and identification of novel mutations in a multicentre cohort of patients with hereditary factor X deficiency.

Mitchell M, Gattens M, Kavakli K, Liesner R, Payne J, Norton M, Austin S. Mitchell M, et al. Blood Coagul Fibrinolysis. 2019 Jan;30(1):34-41. doi: 10.1097/MBC.0000000000000787. Blood Coagul Fibrinolysis. 2019. PMID: 30507709

9

Severe factor XI deficiency caused by compound heterozygosity.

Dai L, Mitchell M, Carson P, Creagh D, Cutler J, Savidge G, Alhaq A. Dai L, et al. Among authors: mitchell m. Br J Haematol. 2004 Jun;125(6):817-8. doi: 10.1111/j.1365-2141.2004.04979.x. Br J Haematol. 2004. PMID: 15180874 Free article. No abstract available.

10

Stabilization of fibrin clots by activated prothrombin complex concentrate and tranexamic acid in FVIII inhibitor plasma.

Dai L, Bevan D, Rangarajan S, Sørensen B, Mitchell M. Dai L, et al. Among authors: mitchell m. Haemophilia. 2011 Sep;17(5):e944-8. doi: 10.1111/j.1365-2516.2011.02491.x. Epub 2011 Mar 3. Haemophilia. 2011. PMID: 21371192

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