Found: 22
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X-linked thrombocytopenia with thalassemia displays bone marrow reticulin fibrosis and enhanced angiogenesis: Comparisons with primary myelofibrosis.
- Published in:
- American Journal of Hematology, 2015, v. 90, n. 3, p. E44, doi. 10.1002/ajh.23907
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- Publication type:
- Article
Indications of underdiagnosis of atypical haemolytic uraemic syndrome in a cohort referred to the Coagulation Unit in Malmo, Sweden, for analysis of ADAMTS13 2007-2012.
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- Nephrology, 2017, v. 22, n. 7, p. 555, doi. 10.1111/nep.12818
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- Article
Patients Referred for Bleeding Symptoms of Unknown Cause: Does Evaluation of Thrombin Generation Contribute to Diagnosis?
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- Mediterranean Journal of Hematology & Infectious Diseases, 2016, v. 8, p. 1, doi. 10.4084/MJHID.2016.014
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- Article
A simplified flow cytometric method for detection of inherited platelet disorders—A comparison to the gold standard light transmission aggregometry.
- Published in:
- PLoS ONE, 2019, v. 14, n. 1, p. 1, doi. 10.1371/journal.pone.0211130
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- Article
Platelet function testing: Current practice among clinical centres in Northern Europe.
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- Haemophilia, 2022, v. 28, n. 4, p. 642, doi. 10.1111/hae.14578
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- Publication type:
- Article
Collagen remodelling and plasma ascorbic acid levels in patients suspected of inherited bleeding disorders harbouring germline variants in collagen‐related genes.
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- Haemophilia, 2021, v. 27, n. 1, p. e69, doi. 10.1111/hae.14195
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- Article
Genetic screening of children with suspected inherited bleeding disorders.
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- Haemophilia, 2020, v. 26, n. 2, p. 314, doi. 10.1111/hae.13948
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- Article
Coagulation factor VIII is vital for increasing global coagulation after physical exercise.
- Published in:
- Haemophilia, 2019, v. 25, n. 2, p. e86, doi. 10.1111/hae.13652
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- Publication type:
- Article
Evaluation of a standardized protocol for thrombin generation using the calibrated automated thrombogram: A Nordic study.
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- Haemophilia, 2019, v. 25, n. 2, p. 334, doi. 10.1111/hae.13640
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- Publication type:
- Article
Expression of cox-2, tie-2 and glycodelin by megakaryocytes in patients with chronic myeloid leukaemia and polycythaemia vera.
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- British Journal of Haematology, 2003, v. 121, n. 3, p. 497, doi. 10.1046/j.1365-2141.2003.04289.x
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- Article
A nonneutralizing antibody as cause of prothrombin deficiency in a patient with follicular lymphoma.
- Published in:
- 2024
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- Publication type:
- Case Study
Prevention and treatment of atherosclerosis in haemophilia - how to balance risk of bleeding with risk of ischaemic events.
- Published in:
- European Journal of Haematology, 2015, v. 94, p. 23, doi. 10.1111/ejh.12498
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- Publication type:
- Article
Angiogenesis is increased in advanced haemophilic joint disease and characterised by normal pericyte coverage.
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- European Journal of Haematology, 2014, v. 92, n. 3, p. 256, doi. 10.1111/ejh.12227
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- Publication type:
- Article
Correlation between serum level of soluble L-selectin and leukocyte count in chronic myeloid and lymphocytic leukemia and during bone marrow transplantation.
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- European Journal of Haematology, 1993, v. 51, n. 2, p. 113, doi. 10.1111/j.1600-0609.1993.tb01603.x
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- Publication type:
- Article
Low pericyte coverage of endometrial microvessels in heavy menstrual bleeding correlates with the microvessel expression of VEGF-A.
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- International Journal of Molecular Medicine, 2015, v. 35, n. 2, p. 433, doi. 10.3892/ijmm.2014.2035
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- Publication type:
- Article
Acquired Haemophilia A in four north European countries: survey of 181 patients.
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- British Journal of Haematology, 2023, v. 201, n. 2, p. 326, doi. 10.1111/bjh.18611
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- Publication type:
- Article
Outcome of an enhanced diagnostic pipeline for patients suspected of inherited thrombocytopenia.
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- British Journal of Haematology, 2019, v. 186, n. 2, p. 373, doi. 10.1111/bjh.15886
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- Publication type:
- Article
Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia.
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- British Journal of Haematology, 2017, v. 179, n. 2, p. 308, doi. 10.1111/bjh.14863
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- Publication type:
- Article
Clinical characterization and identification of rare genetic variants in atypical hemolytic uremic syndrome: A Swedish retrospective observational study.
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- Therapeutic Apheresis & Dialysis, 2021, v. 25, n. 6, p. 988, doi. 10.1111/1744-9987.13634
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- Publication type:
- Article
At the Cross Section of Thrombotic Microangiopathy and Atypical Hemolytic Uremic Syndrome: A Narrative Review of Differential Diagnostics and a Problematization of Nomenclature.
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- Therapeutic Apheresis & Dialysis, 2017, v. 21, n. 4, p. 304, doi. 10.1111/1744-9987.12535
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- Publication type:
- Article
A novel immunohistochemical sequential multi-labelling and erasing technique enables epitope characterization of bone marrow pericytes in primary myelofibrosis.
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- Histopathology, 2012, v. 60, n. 4, p. 554, doi. 10.1111/j.1365-2559.2011.04104.x
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- Publication type:
- Article
Severe Congenital Thrombocytopenia Characterized by Decreased Platelet Sialylation and Moderate Complement Activation Caused by Novel Compound Heterozygous Variants in GNE.
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- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.777402
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- Publication type:
- Article