Found: 24
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Clinical features and molecular analysis of seven British kindreds with hereditary hyperferritinaemia cataract syndrome.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 790, doi. 10.1038/sj.ejhg.5201252
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- Article
TEG PlateletMapping assay results may be misleading in the presence of cold stored platelets.
- Published in:
- 2020
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- Publication type:
- journal article
Delays by patients in seeking treatment for acute chest pain: implications for achieving earlier thrombolysis.
- Published in:
- Postgraduate Medical Journal, 1999, p. 90, doi. 10.1136/pgmj.75.880.90
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- Article
Clinical phenotype, laboratory features and genotype of 35 patients with heritable dysfibrinogenaemia.
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- British Journal of Haematology, 2013, v. 160, n. 2, p. 220, doi. 10.1111/bjh.12085
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- Article
Guideline on the management of bleeding in patients on antithrombotic agents.
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- British Journal of Haematology, 2013, v. 160, n. 1, p. 35, doi. 10.1111/bjh.12107
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- Publication type:
- Article
p.Tyr365Cys change in factor VIII: haemophilia A, but not as we know it.
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- British Journal of Haematology, 2011, v. 154, n. 5, p. 618, doi. 10.1111/j.1365-2141.2011.08688.x
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- Publication type:
- Article
The protein C ω-loop substitution Asn2Ile is associated with reduced protein C anticoagulant activity.
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- British Journal of Haematology, 2009, v. 144, n. 6, p. 946, doi. 10.1111/j.1365-2141.2008.07550.x
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- Article
A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO.
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- British Journal of Haematology, 2006, v. 135, n. 5, p. 603, doi. 10.1111/j.1365-2141.2006.06343.x
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- Article
Severe prekallikrein deficiency associated with homozygosity for an Arg94Stop nonsense mutation.
- Published in:
- British Journal of Haematology, 2004, v. 127, n. 2, p. 220, doi. 10.1111/j.1365-2141.2004.05180.x
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- Article
A Tyr346→Cys substitution in the interdomain acidic region a1 of factor VIII in an individual with factor VIII:C assay discrepancy.
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- British Journal of Haematology, 2002, v. 118, n. 2, p. 589, doi. 10.1046/j.1365-2141.2002.03617.x
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- Publication type:
- Article
Marked elevation of thrombin generation in patients with elevated FVIII:C and venous thromboembolism.
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- British Journal of Haematology, 2001, v. 115, n. 3, p. 687, doi. 10.1046/j.1365-2141.2001.03146.x
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- Publication type:
- Article
Bleeding symptoms and coagulation abnormalities in 337 patients with AL-amyloidosis.
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- British Journal of Haematology, 2000, v. 110, n. 2, p. 454, doi. 10.1046/j.1365-2141.2000.02183.x
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- Publication type:
- Article
Advances in understanding the pathogenesis of hereditary macrothrombocytopenia.
- Published in:
- British Journal of Haematology, 2021, v. 195, n. 1, p. 25, doi. 10.1111/bjh.17409
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- Publication type:
- Article
Guidelines for the use of platelet transfusions.
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- British Journal of Haematology, 2017, v. 176, n. 3, p. 365, doi. 10.1111/bjh.14423
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- Article
Guideline for the diagnosis and management of the rare coagulation disorders.
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- British Journal of Haematology, 2014, v. 167, n. 3, p. 304, doi. 10.1111/bjh.13058
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- Publication type:
- Article
Prospective observational cohort study of the association between thromboelastometry, coagulation and platelet parameters and bleeding in patients with haematological malignancies- The ATHENA study.
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- British Journal of Haematology, 2014, v. 166, n. 4, p. 581, doi. 10.1111/bjh.12928
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- Publication type:
- Article
Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia.
- Published in:
- 2017
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- Publication type:
- journal article
Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2.
- Published in:
- BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-42
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- Publication type:
- Article
Factor VII deficiency and the FVII mutation database.
- Published in:
- Human Mutation, 2001, v. 17, n. 1, p. 3, doi. 10.1002/1098-1004(2001)17:1<3::AID-HUMU2>3.0.CO;2-V
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- Publication type:
- Article
Tissue Factor in the myocardium: Evidence of roles in haemostasis and inflammation.
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- Disease Markers, 2004, v. 20, n. 6, p. 353, doi. 10.1155/2004/963402
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- Publication type:
- Article
Differential effects of direct factor IIa and factor Xa inhibitors in protein C‐deficient plasma detected using thrombin generation and viscoelastometry assays.
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- International Journal of Laboratory Hematology, 2020, v. 42, n. 2, p. 126, doi. 10.1111/ijlh.13126
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- Article
Cerebral palsy in siblings caused by compound heterozygous mutations in the gene encoding protein C.
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- Developmental Medicine & Child Neurology, 2010, v. 52, n. 5, p. 489, doi. 10.1111/j.1469-8749.2010.03618.x
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- Publication type:
- Article
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.
- Published in:
- 2020
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- Publication type:
- journal article
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].
- Published in:
- PLoS ONE, 2015, v. 10, n. 12, p. 1, doi. 10.1371/journal.pone.0144984
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- Publication type:
- Article