Mitchell M - Search Results

1

A Novel Homozygous c.800C>G Substitution in GP1BA Exon 2 in a Kuwaiti Family with Bernard-Soulier Syndrome.

Shlebak A, Poles A, Manning R, Almuhareb S, De La Funte J, Mitchell M, Lucas G. Shlebak A, et al. Among authors: mitchell m. Acta Haematol. 2015;134(3):193-8. doi: 10.1159/000381328. Epub 2015 May 28. Acta Haematol. 2015. PMID: 26044173

2

A diagnostic dilemma: variant Bernard-Soulier syndrome, a difficult clinical and genetic diagnosis.

Okoli S, Madan B, Mwirigi A, Moore G, Drew A, Mitchell MJ, Cutler JA. Okoli S, et al. Among authors: mitchell mj. Haemophilia. 2015 Nov;21(6):e510-3. doi: 10.1111/hae.12777. Epub 2015 Jul 31. Haemophilia. 2015. PMID: 26226975 No abstract available.

3

Molecular characterization of 11 novel mutations in patients with heterozygous and homozygous FV deficiency.

Cutler JA, Patel R, Rangarajan S, Tait RC, Mitchell MJ. Cutler JA, et al. Among authors: mitchell mj. Haemophilia. 2010 Nov;16(6):937-42. doi: 10.1111/j.1365-2516.2010.02330.x. Haemophilia. 2010. PMID: 20546033

4

The first report of a multi-exon duplication in the F9 gene causative of severe haemophilia B.

Wheeler RB, Cutler JA, Alamelu J, Mitchell MJ. Wheeler RB, et al. Among authors: mitchell mj. Haemophilia. 2015 Sep;21(5):e433-5. doi: 10.1111/hae.12735. Epub 2015 Jul 17. Haemophilia. 2015. PMID: 26389844 No abstract available.

5

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

6

Identification of a novel mutation in a non-Jewish factor XI deficient kindred.

Alhaq A, Mitchell M, Sethi M, Rahman S, Flynn G, Boulton P, Caeno G, Smith M, Savidge G. Alhaq A, et al. Among authors: mitchell m. Br J Haematol. 1999 Jan;104(1):44-9. doi: 10.1046/j.1365-2141.1999.01150.x. Br J Haematol. 1999. PMID: 10027710 Free article.

7

A novel mutation in the P2Y12 receptor and a function-reducing polymorphism in protease-activated receptor 1 in a patient with chronic bleeding.

Patel YM, Lordkipanidzé M, Lowe GC, Nisar SP, Garner K, Stockley J, Daly ME, Mitchell M, Watson SP, Austin SK, Mundell SJ. Patel YM, et al. Among authors: mitchell m. J Thromb Haemost. 2014 May;12(5):716-25. doi: 10.1111/jth.12539. J Thromb Haemost. 2014. PMID: 24612435 Free article.

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

Rapid genetic diagnosis in neonatal pulmonary artery thrombosis caused by homozygous antithrombin Budapest 3.

Brown SA, Mitchell M, Cutler JA, Moore G, Smith MP, Savidge GF. Brown SA, et al. Among authors: mitchell m. Clin Appl Thromb Hemost. 2000 Jul;6(3):181-3. doi: 10.1177/107602960000600312. Clin Appl Thromb Hemost. 2000. PMID: 10898281 Free article.

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

4,479 results

Search Page

Filters