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Alterations of T cell receptor Vβ repertoire of CD8 T lymphocytes in immune tolerance induction in two hemophilia A patients with inhibitors.
- Published in:
- Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2011, v. 68, n. 12, p. 1047, doi. 10.2298/VSP1112047S
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- Publication type:
- Article
Correction to: Efficacy and safety of full-length pegylated recombinant factor VIII with extended half-life in previously treated patients with hemophilia A: comparison of data between the general and Japanese study populations.
- Published in:
- 2018
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- Publication type:
- journal article
First report of real-time monitoring of coagulation function potential and IgG subtype of anti-FVIII autoantibodies in a child with acquired hemophilia A associated with streptococcal infection and amoxicillin.
- Published in:
- 2018
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- Publication type:
- journal article
Efficacy and safety of full-length pegylated recombinant factor VIII with extended half-life in previously treated patients with hemophilia A: comparison of data between the general and Japanese study populations.
- Published in:
- 2017
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- Publication type:
- journal article
Potentially life-threatening coagulopathy associated with simultaneous reduction in coagulation and fibrinolytic function in pediatric acute leukemia after hematopoietic stem-cell transplantation.
- Published in:
- 2017
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- Publication type:
- journal article
Analysis of the Japanese subgroup in LEOPOLD II: a phase 2/3 study of BAY 81-8973, a new recombinant factor VIII product.
- Published in:
- 2017
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- Publication type:
- journal article
A combined approach using global coagulation assays quickly differentiates coagulation disorders with prolonged aPTT and low levels of FVIII activity.
- Published in:
- 2017
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- Publication type:
- journal article
Pediatric thromboembolism: a national survey in Japan.
- Published in:
- 2017
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- Publication type:
- journal article
Use of a microchip flow-chamber system as a screening test for platelet storage pool disease.
- Published in:
- International Journal of Hematology, 2015, v. 102, n. 2, p. 157, doi. 10.1007/s12185-015-1819-8
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- Publication type:
- Article
SVA retrotransposition in exon 6 of the coagulation factor IX gene causing severe hemophilia B.
- Published in:
- 2015
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- Publication type:
- Journal Article
The International Immune Tolerance Induction Study and its follow-up study on Japanese hemophilia A patients with inhibitors.
- Published in:
- International Journal of Hematology, 2015, v. 101, n. 4, p. 362, doi. 10.1007/s12185-015-1734-z
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- Publication type:
- Article
Optimization of the automated, CS-2000i™ method for measuring low levels of von Willebrand factor ristocetin cofactor activity (VWF:RCo).
- Published in:
- 2015
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- Publication type:
- journal article
Optimization of the automated, CS-2000i™ method for measuring low levels of von Willebrand factor ristocetin cofactor activity (VWF:RCo).
- Published in:
- International Journal of Hematology, 2015, v. 101, n. 2, p. 126, doi. 10.1007/s12185-014-1720-x
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- Publication type:
- Article
Tissue factor pathway inhibitor in activated prothrombin complex concentrates (aPCC) moderates the effectiveness of therapy in some severe hemophilia A patients with inhibitor.
- Published in:
- International Journal of Hematology, 2014, v. 99, n. 5, p. 577, doi. 10.1007/s12185-014-1572-4
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- Publication type:
- Article
Incidence and survival rates of hematological malignancies in Japanese children and adolescents (2006-2010): based on registry data from the Japanese Society of Pediatric Hematology.
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- International Journal of Hematology, 2013, v. 98, n. 1, p. 74, doi. 10.1007/s12185-013-1364-2
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- Publication type:
- Article
Report of the Fifth meeting of the International Network for Pediatric Hemophilia: a focus on prophylaxis and immune tolerance induction.
- Published in:
- 2011
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- Publication type:
- research
A modified thrombin generation test for investigating very low levels of factor VIII activity in hemophilia A.
- Published in:
- 2009
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- Publication type:
- journal article
Factor VIII-mediated global hemostasis in the absence of von Willebrand factor.
- Published in:
- 2007
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- Publication type:
- journal article
Relationship between the binding sites for von Willebrand factor, phospholipid, and human factor VIII C2 inhibitor alloantibodies within the factor VIII C2 domain.
- Published in:
- 2007
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- Publication type:
- journal article
Superficial fibromatosis mimicking subcutaneous hematoma: an unusual and difficult diagnosis in a patient with mild hemophilia A.
- Published in:
- 2007
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- Publication type:
- journal article
Characterization of factor VIII inhibitors.
- Published in:
- 2006
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- Publication type:
- journal article
Highly conserved antigenic structure of the factor VIII C2 domain in some mammals.
- Published in:
- 2005
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- Publication type:
- journal article
Inversions of the factor VIII gene in Japanese patients with severe hemophilia A.
- Published in:
- 2004
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- Publication type:
- journal article
The Prevalence of Neutralizing Antibodies Against Adeno-Associated Virus Capsids Is Reduced in Young Japanese Individuals.
- Published in:
- Journal of Medical Virology, 2014, v. 86, n. 11, p. 1990, doi. 10.1002/jmv.23818
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- Publication type:
- Article
Successful unrelated cord blood transplantation for Diamond–Blackfan anemia.
- Published in:
- 2021
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- Publication type:
- Case Study
A microchip flow‐chamber assay screens congenital primary hemostasis disorders.
- Published in:
- Pediatrics International, 2021, v. 63, n. 2, p. 160, doi. 10.1111/ped.14378
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- Publication type:
- Article
Pulmonary hypertension with diffuse lung lesions in cobalamin C defect.
- Published in:
- 2019
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- Publication type:
- Case Study
Hemostatic function in hyperfibrinolytic disseminated intravascular coagulation.
- Published in:
- Pediatrics International, 2019, v. 61, n. 9, p. 872, doi. 10.1111/ped.13919
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- Publication type:
- Article
Pediatric phantom tumor caused by cardiac catheterization.
- Published in:
- 2019
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- Publication type:
- Case Study
Fibrinolytic abnormality associated with progression of pediatric solid tumor.
- Published in:
- Pediatrics International, 2018, v. 60, n. 6, p. 540, doi. 10.1111/ped.13546
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- Publication type:
- Article
Influenza-associated thrombotic microangiopathy with unbalanced von Willebrand factor and a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 levels in a heterozygous protein S-deficient boy.
- Published in:
- Pediatrics International, 2016, v. 58, n. 9, p. 926, doi. 10.1111/ped.13014
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- Publication type:
- Article
Protein C deficiency as the major cause of thrombophilias in childhood.
- Published in:
- Pediatrics International, 2013, v. 55, n. 3, p. 267, doi. 10.1111/ped.12102
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- Publication type:
- Article
Patient Report Ecthyma gangrenosum combined with multiple perforations of the small intestine associated with Pseudomonas aeruginosa.
- Published in:
- Pediatrics International, 2004, v. 46, n. 1, p. 104, doi. 10.1111/j.1328-0867.2004..x
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- Publication type:
- Article
A case of West syndrome with atypical massive gray matter heterotopia that is well controlled by ACTH therapy.
- Published in:
- Pediatrics International, 1996, v. 38, n. 3, p. 274, doi. 10.1111/j.1442-200X.1996.tb03486.x
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- Publication type:
- Article
Current and future therapies for haemophilia—Beyond factor replacement therapies.
- Published in:
- British Journal of Haematology, 2023, v. 200, n. 1, p. 23, doi. 10.1111/bjh.18379
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- Publication type:
- Article
Prediction of the haemostatic effects of bypassing therapy using comprehensive coagulation assays in emicizumab prophylaxis‐treated haemophilia A patients with inhibitors.
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- British Journal of Haematology, 2020, v. 190, n. 5, p. 727, doi. 10.1111/bjh.16574
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- Publication type:
- Article
A novel simultaneous clot‐fibrinolysis waveform analysis for assessing fibrin formation and clot lysis in haemorrhagic disorders.
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- British Journal of Haematology, 2019, v. 187, n. 4, p. 518, doi. 10.1111/bjh.16111
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- Publication type:
- Article
Emicizumab‐mediated haemostatic function in patients with haemophilia A is down‐regulated by activated protein C through inactivation of activated factor V.
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- British Journal of Haematology, 2018, v. 183, n. 2, p. 257, doi. 10.1111/bjh.15525
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- Publication type:
- Article
Factor (F)VIII/VIIa enhances global haemostatic function in the co-presence of bypassing agents and FVIII among patients with haemophilia A with inhibitor.
- Published in:
- British Journal of Haematology, 2018, v. 181, n. 4, p. 528, doi. 10.1111/bjh.15209
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- Publication type:
- Article
Identification of novel kinase fusion transcripts in paediatric B cell precursor acute lymphoblastic leukaemia with IKZF1 deletion.
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- British Journal of Haematology, 2015, v. 171, n. 5, p. 813, doi. 10.1111/bjh.13757
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- Publication type:
- Article
Different factor VIII neutralizing effects on anti-factor VIII inhibitor antibodies associated with epitope specificity and von Willebrand factor.
- Published in:
- British Journal of Haematology, 2013, v. 163, n. 1, p. 104, doi. 10.1111/bjh.12473
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- Publication type:
- Article
Terminus‐Selective Covalent Immobilization of Heparin on a Thermoresponsive Surface Using Click Chemistry for Efficient Binding of Basic Fibroblast Growth Factor.
- Published in:
- Macromolecular Bioscience, 2024, v. 24, n. 2, p. 1, doi. 10.1002/mabi.202300307
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- Publication type:
- Article
Delivery of Full-Length Factor VIII Using a <i>piggyBac</i> Transposon Vector to Correct a Mouse Model of Hemophilia A.
- Published in:
- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0104957
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- Publication type:
- Article
A Novel Cell-Sheet Technology That Achieves Durable Factor VIII Delivery in a Mouse Model of Hemophilia A.
- Published in:
- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0083280
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- Publication type:
- Article
Current status and future prospects of activated recombinant coagulation factor VIIa, NovoSeven®, in the treatment of haemophilia and rare bleeding disorders.
- Published in:
- Annals of Hematology, 2024, v. 103, n. 8, p. 2647, doi. 10.1007/s00277-023-05287-2
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- Publication type:
- Article
Lupus anticoagulant hypoprothrombinemia syndrome in Bence-Jones protein κ-type multiple myeloma patient with phosphatidylserine-dependent antiprothrombin antibody.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Lupus anticoagulant hypoprothrombinemia syndrome in Bence-Jones protein κ-type multiple myeloma patient with phosphatidylserine-dependent antiprothrombin antibody.
- Published in:
- 2013
- By:
- Publication type:
- Case Study
Fraction and Number of Unemployed Associated with Self-Reported Low Back Pain: A Nation-Wide Cross-Sectional Study in Japan.
- Published in:
- International Journal of Environmental Research & Public Health, 2021, v. 18, n. 20, p. 10760, doi. 10.3390/ijerph182010760
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- Publication type:
- Article
Occupational status and self-reported low back pain by gender: a nation-wide cross-sectional study among the general population in Japan.
- Published in:
- Environmental Health & Preventive Medicine, 2021, v. 26, n. 1, p. 1, doi. 10.1186/s12199-021-01031-2
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- Publication type:
- Article
Correlations between global clotting function tests, duration of operation, and postoperative chest tube drainage in pediatric cardiac surgery.
- Published in:
- Pediatric Anesthesia, 2011, v. 21, n. 8, p. 865, doi. 10.1111/j.1460-9592.2011.03524.x
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- Publication type:
- Article