111 results on '"Mumford, Andrew D."'
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2. Scoping Review of Factors Associated with Stem Cell Mobilization and Collection in Allogeneic Stem Cell Donors
3. The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants
4. Functional filter for whole-genome sequencing data identifies HHT and stress-associated non-coding SMAD4 polyadenylation site variants >5 kb from coding DNA
5. PIK3R3 is a candidate regulator of platelet count in people of Bangladeshi ancestry
6. How I diagnose and treat neonatal thrombocytopenia
7. Prediction of Bleeding in Pediatric Cardiac Surgery Using Clinical Characteristics and Prospective Coagulation Test Results
8. Monoallelic loss-of-function THPO variants cause heritable thrombocytopenia
9. Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC
10. Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders
11. Near‐patient coagulation testing to predict bleeding after cardiac surgery: a cohort study
12. A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss
13. A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders
14. VPS33B regulates protein sorting into and maturation of α-granule progenitor organelles in mouse megakaryocytes
15. Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia
16. A multi-centre randomised controlled trial of Transfusion Indication Threshold Reduction on transfusion rates, morbidity and healthcare resource use following cardiac surgery: Study protocol
17. Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assay
18. High haematocrit in cyanotic congenital heart disease affects how fibrinogen activity is determined by rotational thromboelastometry
19. The risk of hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type 2
20. Guidelines for the use of platelet transfusions
21. Evaluation of multiple electrode aggregometry in whole blood using Multiplate® Mini Test cells
22. A novel thromboxane A2 receptor D304N variant that abrogates ligand binding in a patient with a bleeding diathesis
23. Clinically Significant Pulmonary Barotrauma After Inflation Of Party Balloons
24. Guideline for the diagnosis and management of the rare coagulation disorders: A United Kingdom Haemophilia Centre Doctorsʼ Organization guideline on behalf of the British Committee for Standards in Haematology
25. Prospective observational cohort study of the association between thromboelastometry, coagulation and platelet parameters and bleeding in patients with haematological malignancies- The ATHENA study
26. Clinical phenotype, laboratory features and genotype of 35 patients with heritable dysfibrinogenaemia
27. Guideline on the management of bleeding in patients on antithrombotic agents
28. p.Tyr365Cys change in factor VIII: haemophilia A, but not as we know it
29. Cerebral palsy in siblings caused by compound heterozygous mutations in the gene encoding protein C
30. A novel missense mutation in ABCA1 results in altered protein trafficking and reduced phosphatidylserine translocation in a patient with Scott syndrome
31. The protein C ω-loop substitution Asn2Ile is associated with reduced protein C anticoagulant activity
32. A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO
33. Severe prekallikrein deficiency associated with homozygosity for an Arg94Stop nonsense mutation
34. Advances in understanding the pathogenesis of hereditary macrothrombocytopenia.
35. A Tyr346→Cys substitution in the interdomain acidic region a1 of factor VIII in an individual with factor VIII:C assay discrepancy
36. Marked elevation of thrombin generation in patients with elevated FVIII:C and venous thromboembolism
37. Bleeding symptoms and coagulation abnormalities in 337 patients with AL-amyloidosis
38. The lens in hereditary hyperferritinaemia cataract syndrome contains crystalline deposits of L-ferritin
39. Pharmacodynamic Comparison of Ticagrelor Monotherapy Versus Ticagrelor and Aspirin in Patients After Percutaneous Coronary Intervention: The TEMPLATE (Ticagrelor Monotherapy and Platelet Reactivity) Randomized Controlled Trial.
40. FLNA variants associated with disorders of platelet number or function.
41. TEG PlateletMapping assay results may be misleading in the presence of cold stored platelets.
42. Differential effects of direct factor IIa and factor Xa inhibitors in protein C‐deficient plasma detected using thrombin generation and viscoelastometry assays.
43. Genetic Techniques Used in the Diagnosis of Inherited Platelet Disorders.
44. Protease-Activated Receptor 4 Variant p.Tyr157Cys Reduces Platelet Functional Responses and Alters Receptor Trafficking.
45. TUBB1 variants and human platelet traits.
46. A Study of Platelet Inhibition, Using a ‘Point of Care’ Platelet Function Test, following Primary Percutaneous Coronary Intervention for ST-Elevation Myocardial Infarction [PINPOINT-PPCI].
47. A review of platelet secretion assays for the diagnosis of inherited platelet secretion disorders.
48. Diversity and impact of rare variants in genes encoding the platelet G protein-coupled receptors.
49. ACTN1 variants associated with thrombocytopenia.
50. Partial deletion of the αC-domain in the Fibrinogen Perth variant is associated with thrombosis, increased clot strength and delayed fibrinolysis.
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