Found: 28
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Antithrombin and fibrinogen levels as predictors for plasma L-asparaginase activity in children with acute lymphoblastic leukemia.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Increased fibrinolysis-induced bradykinin formation in hereditary angioedema confirmed using stored plasma and biotechnological inhibitors.
- Published in:
- BMC Research Notes, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13104-019-4335-8
- By:
- Publication type:
- Article
Glanzmann thrombasthenia in an Oldenbourg filly.
- Published in:
- Veterinary Clinical Pathology, 2007, v. 36, n. 2, p. 204, doi. 10.1111/j.1939-165X.2007.tb00211.x
- By:
- Publication type:
- Article
Identification of a Reliable Biomarker Profile for the Diagnosis of Gaucher Disease Type 1 Patients Using a Mass Spectrometry-Based Metabolomic Approach.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 21, p. 7869, doi. 10.3390/ijms21217869
- By:
- Publication type:
- Article
Glanzmann thrombasthenia platelets compete with transfused platelets, reducing the haemostatic impact of platelet transfusions.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Comparing Pathways of Bradykinin Formation in Whole Blood From Healthy Volunteers and Patients With Hereditary Angioedema Due to C1 Inhibitor Deficiency.
- Published in:
- Frontiers in Immunology, 2018, p. 1, doi. 10.3389/fimmu.2018.02183
- By:
- Publication type:
- Article
From Principle to Practice: Bridging the Gap in Patient Profiling.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0054728
- By:
- Publication type:
- Article
The diagnosis of hereditary angioedema with C1 inhibitor deficiency: a survey of Canadian physicians and laboratories.
- Published in:
- Allergy, Asthma & Clinical Immunology, 2018, v. 14, n. 1, p. N.PAG, doi. 10.1186/s13223-018-0307-0
- By:
- Publication type:
- Article
Incidence of thrombotic microangiopathies in Quebec: insight from a laboratory centralizing ADAMTS-13 testing.
- Published in:
- Orphanet Journal of Rare Diseases, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s13023-022-02409-3
- By:
- Publication type:
- Article
c-Met activation in medulloblastoma induces tissue factor expression and activity: effects on cell migration.
- Published in:
- Carcinogenesis, 2009, v. 30, n. 7, p. 1089, doi. 10.1093/carcin/bgp085
- By:
- Publication type:
- Article
Acquired thrombotic thrombocytopenic purpura with isolated CFHR3/1 deletion—rapid remission following complement blockade.
- Published in:
- Pediatric Nephrology, 2018, v. 33, n. 8, p. 1437, doi. 10.1007/s00467-018-3957-8
- By:
- Publication type:
- Article
Generation of kinins during preparation and storage of whole blood–derived platelet concentrates.
- Published in:
- Transfusion, 2007, v. 47, n. 3, p. 410, doi. 10.1111/j.1537-2995.2007.01097.x
- By:
- Publication type:
- Article
L-Asparaginase lowers plasma antithrombin and mannan-binding-lectin levels: Impact on thrombotic and infectious events in children with acute lymphoblastic leukemia.
- Published in:
- Pediatric Blood & Cancer, 2015, v. 62, n. 8, p. 1381, doi. 10.1002/pbc.25515
- By:
- Publication type:
- Article
Glanzmann Thrombasthenia: Perspectives from Clinical Practice on Accurate Diagnosis and Optimal Treatment Strategies.
- Published in:
- Journal of Blood Medicine, 2021, v. 12, p. 449, doi. 10.2147/JBM.S271744
- By:
- Publication type:
- Article
Examination of genetic variants involved in generation and biodisposition of kinins in patients with angioedema.
- Published in:
- Allergy, Asthma & Clinical Immunology, 2014, v. 10, n. 1, p. 1, doi. 10.1186/s13223-014-0060-y
- By:
- Publication type:
- Article
Tissue factor mediates the HGF/Met-induced anti-apoptotic pathway in DAOY medulloblastoma cells.
- Published in:
- Journal of Neuro-Oncology, 2010, v. 97, n. 3, p. 365, doi. 10.1007/s11060-009-0041-z
- By:
- Publication type:
- Article
A novel FGG missense variant associated with fibrinogen storage disease in a large family from Quebec.
- Published in:
- Haemophilia, 2024, v. 30, n. 3, p. 858, doi. 10.1111/hae.15006
- By:
- Publication type:
- Article
Deciphering a novel complex inversion affecting F8 in a family with severe haemophilia A by optical genome mapping.
- Published in:
- Haemophilia, 2023, v. 29, n. 3, p. 921, doi. 10.1111/hae.14771
- By:
- Publication type:
- Article
Switching to emicizumab: A prospective surveillance study in haemophilia A subjects with inhibitors.
- Published in:
- Haemophilia, 2023, v. 29, n. 1, p. 348, doi. 10.1111/hae.14685
- By:
- Publication type:
- Article
Immune tolerance induction using Fc‐fusion‐protein recombinant factor IX in severe haemophilia B.
- Published in:
- Haemophilia, 2021, v. 27, n. 6, p. e776, doi. 10.1111/hae.14424
- By:
- Publication type:
- Article
Evaluation of anti‐factor VIII antibodies in haemophilia A subjects switching products following a provincial tender.
- Published in:
- Haemophilia, 2022, v. 28, n. 1, p. e1, doi. 10.1111/hae.14434
- By:
- Publication type:
- Article
A full molecular picture of F8 intron 1 inversion created with optical genome mapping.
- Published in:
- Haemophilia, 2021, v. 27, n. 5, p. e638, doi. 10.1111/hae.14375
- By:
- Publication type:
- Article
A prospective surveillance study in haemophilia B patients following a population switch to recombinant factor IX (nonacog gamma).
- Published in:
- Haemophilia, 2021, v. 27, n. 4, p. e530, doi. 10.1111/hae.14273
- By:
- Publication type:
- Article
The diagnosis of a haemophilia A carrier over 2 decades.
- Published in:
- Haemophilia, 2021, v. 27, n. 1, p. e133, doi. 10.1111/hae.14073
- By:
- Publication type:
- Article
The challenge of genetically unresolved haemophilia A patients: Interest of the combination of whole F8 gene sequencing and functional assays.
- Published in:
- Haemophilia, 2020, v. 26, n. 6, p. 1056, doi. 10.1111/hae.14179
- By:
- Publication type:
- Article
Acquired haemophilia A and concomitant factor XIII consumption.
- Published in:
- Haemophilia, 2019, v. 25, n. 3, p. e180, doi. 10.1111/hae.13690
- By:
- Publication type:
- Article
Relapse pattern and long‐term outcomes in subjects with acquired haemophilia A.
- Published in:
- Haemophilia, 2019, v. 25, n. 2, p. 252, doi. 10.1111/hae.13685
- By:
- Publication type:
- Article
Challenges in diagnosis of von Willebrand disease in the presence of combined mutations of different genes.
- Published in:
- 2019
- By:
- Publication type:
- Case Study