Myers B - Search Results

1

A comprehensive targeted next-generation sequencing panel for genetic diagnosis of patients with suspected inherited thrombocytopenia.

Johnson B, Doak R, Allsup D, Astwood E, Evans G, Grimley C, James B, Myers B, Stokley S, Thachil J, Wilde J, Williams M, Makris M, Lowe GC, Wallis Y, Daly ME, Morgan NV; UK GAPP Study Group. Johnson B, et al. Among authors: myers b. Res Pract Thromb Haemost. 2018 Oct 8;2(4):640-652. doi: 10.1002/rth2.12151. eCollection 2018 Oct. Res Pract Thromb Haemost. 2018. PMID: 30349881 Free PMC article.

2

Rare missense variants in Tropomyosin-4 (TPM4) are associated with platelet dysfunction, cytoskeletal defects, and excessive bleeding.

Stapley RJ, Poulter NS, Khan AO, Smith CW, Bignell P, Fratter C, Lester W, Lowe G, Morgan NV; UK GAPP Study Group. Stapley RJ, et al. J Thromb Haemost. 2022 Feb;20(2):478-485. doi: 10.1111/jth.15584. Epub 2021 Nov 21. J Thromb Haemost. 2022. PMID: 34758189 Free article.

3

Investigation of the contribution of an underlying platelet defect in women with unexplained heavy menstrual bleeding.

Lowe GC, Fickowska R, Al Ghaithi R, Maclachlan A, Harrison P, Lester W, Watson SP, Myers B, Clark J, Morgan NV. Lowe GC, et al. Among authors: myers b. Platelets. 2019;30(1):56-65. doi: 10.1080/09537104.2018.1543865. Epub 2018 Dec 6. Platelets. 2019. PMID: 30520671 Free PMC article.

4

A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorder.

Almazni I, Chudakou P, Dawson-Meadows A, Downes K, Freson K, Mason J, Page P, Reay K, Myers B, Morgan NV; UK GAPP Study Group. Almazni I, et al. Among authors: myers b. Platelets. 2022 Feb 17;33(2):320-323. doi: 10.1080/09537104.2021.1887470. Epub 2021 Feb 22. Platelets. 2022. PMID: 33616470 Free article.

5

A Novel, Enriched Population Pharmacokinetic Model for Recombinant Factor VIII-Fc Fusion Protein Concentrate in Hemophilia A Patients.

Bukkems LH, Heijdra JM, Mathias M, Collins PW, Hay CRM, Tait RC, Mangles S, Myers B, Evans G, Bailiff B, Curry N, Payne J, Austin S, Goedhart TMHJ, Leebeek FWG, Meijer K, Fijnvandraat K, Chowdary P, Mathôt RAA, Cnossen MH; for UK-EHL Outcomes Registry OPTI-CLOT Collaboration. Bukkems LH, et al. Among authors: myers b. Thromb Haemost. 2020 May;120(5):747-757. doi: 10.1055/s-0040-1709522. Epub 2020 May 5. Thromb Haemost. 2020. PMID: 32369846

6

Skin, bone marrow and magnetic resonance imaging appearances in systemic mastocytosis.

Myers B, Grimley C, Jones SG, Clark D, Kerslake R. Myers B, et al. Br J Haematol. 2003 Sep;122(6):876. doi: 10.1046/j.1365-2141.2003.04416.x. Br J Haematol. 2003. PMID: 12956756 Free article. No abstract available.

7

Gynaecological management of women with inherited bleeding disorders. A UK Haemophilia Centres Doctors' Organisation Guideline.

Curry N, Bowles L, Clark TJ, Lowe G, Mainwaring J, Mangles S, Myers B, Kadir RA. Curry N, et al. Among authors: myers b. Haemophilia. 2022 Nov;28(6):917-937. doi: 10.1111/hae.14643. Epub 2022 Aug 17. Haemophilia. 2022. PMID: 35976756 Review.

8

Diagnosis and management of maternal thrombocytopenia in pregnancy.

Myers B. Myers B. Br J Haematol. 2012 Jul;158(1):3-15. doi: 10.1111/j.1365-2141.2012.09135.x. Epub 2012 May 3. Br J Haematol. 2012. PMID: 22551110 Free article. Review.

9

A case series review of patients with Thrombocytopenia and Absent-Radii syndrome (TARS) and their management during pregnancy.

Halperin D, Pavord S, Myers B. Halperin D, et al. Among authors: myers b. Platelets. 2021 Nov 17;32(8):1124-1125. doi: 10.1080/09537104.2020.1869716. Epub 2021 Feb 12. Platelets. 2021. PMID: 33577379 Free article. Review.

10

The place of beta 2 glycoprotein 1 in the assessment of antiphospholipid syndrome.

Myers B, Gould J. Myers B, et al. Blood Coagul Fibrinolysis. 2003 Jan;14(1):1-2. doi: 10.1097/00001721-200301000-00001. Blood Coagul Fibrinolysis. 2003. PMID: 12544720

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