132 results on '"Bonduel, M."'
Search Results
2. Managing space requirements of new buildings using linked building data technologies
3. Phenotype–genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8 and X‐chromosome inactivation
4. Diagnosis and management of venous thromboembolism (VTE) in children: a prospective 22-year registry from a single tertiary center in Argentina: OR160
5. Use of warfarin oral suspension for antithrombotic therapy and prevention of thrombosis in infants and children: PHT15
6. Venography (VE) in children with clinical assessment of post-thrombotic syndrome (PTS) following upper venous system thrombotic event (UVSTE): PHT01
7. International pediatric thrombosis network to advance pediatric thrombosis research: Communication from the ISTH SSC subcommittee on pediatric and neonatal thrombosis and hemostasis
8. International pediatric thrombosis network to advance pediatric thrombosis research: Communication from the ISTH SSC subcommittee on pediatric and neonatal thrombosis and hemostasis
9. Inherited antithrombin deficiency: description of a pediatric series in a single center: PO 303
10. Chylothorax in neonates and children: diagnosis and antithrombotic therapy of a complication associated with upper venous system thrombosis (UVST): PB 1.71–3
11. Vitamin K antagonists (VKAs) for venous thromboembolism (VTE) in a pediatric cohort with persistent antiphospholipid antibodies (aPL): PB 1.71–1
12. Low-dose ristocetin induced platelet aggregation. Which dose is low enough?: PB 1.43–6
13. Clinical efficacy and safety of DDAVP with or without tranexamic acid in inherited VWD: final results of the prospective and international study on 229 patients: PA 2.08–1
14. Successful related umbilical cord blood transplantation for graft failure following T cell-depleted non-identical bone marrow transplantation in a child with major histocompatibility complex class II deficiency
15. Impact of persistent antiphospholipid antibodies on symptomatic thromboembolism in children: a systematic review & meta-analysis [observational studies]: O-WE-032
16. Methodology of ristocetin-induced platelet-aggregation (RIPA) mixing studies in type 2b von Willebrand disease: 35P15
17. Frequency of discrepant VWF:RCo/VWF:Ag ratios and thrombocytopenia in a cohort of children with type 2b von Willebrand disease: 35P14
18. Use of recombinant activated factor VII (rFVIIa) in pediatric patients with high bleeding risk: 26P12
19. Antiphospholipid syndrome (APS) in a pediatric cohort with venous thromboembolism: OC-TU-064
20. Unrelated cord blood transplantation and reduced-intensity conditioning regimen for graft failure in a child with Major Histocompatibility Complex class II deficiency
21. Successful treatment of autoimmune hemolytic anemia with rituximab in a child with severe combined immunodeficiency following nonidentical T-cell-depleted bone marrow transplantation
22. Platelet aggregation and adenosine triphosphate release values in children and adults
23. Consensus-based clinical recommendations and research priorities for anticoagulant thromboprophylaxis in children hospitalized for COVID-19-related illness
24. Atypical skin lesions caused by Curvularia sp. and Pseudallescheria boydii in two patients after allogeneic bone marrow transplantation
25. Hospital Transfusion Committee, an Appropriate Tool for the Development, Implementation and Monitoring of Guidelines in the Clinical Use of Blood
26. Acenocoumarol therapy in pediatric patients
27. Phenotypic analysis of human BM T-cell depleted by soybean lectin agglutination and E rosetting with sheep RBC: Relative enrichment of N K cells and a CD3+ ,CD2−dim population
28. Managing Space Requirements of New Buildings Using Linked Building Data Technologies
29. Impact of thrombophilia on risk of arterial ischemic stroke or cerebral sinovenous thrombosis in neonates and children: a systematic review and meta-analysis of observational studies
30. SEGMENTATION OF LARGE UNSTRUCTURED POINT CLOUDS USING OCTREE-BASED REGION GROWING AND CONDITIONAL RANDOM FIELDS
31. SCAN-TO-BIM OUTPUT VALIDATION: TOWARDS A STANDARDIZED GEOMETRIC QUALITY ASSESSMENT OF BUILDING INFORMATION MODELS BASED ON POINT CLOUDS
32. Clinical efficacy and safety of DDAVP with or without tranexamic acid in inherited VWD: final results of the prospective and international study on 229 patients
33. Impact of Persistent Antiphospholipid antibodies on symptomatic thromboembolism in children: A systematic review & meta-analysis (observational studies)
34. Repeat course of rabbit antithymocyte globulin as salvage following initial therapy with rabbit antithymocyte globulin in acquired aplastic anemia
35. Impact ofthrombophilia on risk of arterial ischemic stroke or cerebral sinovenousthrombosis in neonates and children: a systematic review and meta-analysis ofobservational studies
36. Co- polyolefin based nanocomposites via carbon nanotube -supported metallocene catalysis
37. Impact of inherited thrombophilia on venous thromboembolism in children: a systematic review and meta-analysis of observational studies
38. Unrelated cord blood transplantation and reduced-intensity conditioning regimen for graft failure in a child with Major Histocompatibility Complex class II deficiency
39. Hemoglobin San Martin: A New Unstable Variant Associated with Hemoglobin S in an Argentinean Boy.
40. Factor V Leiden Mutation in the Argentinian Population
41. #630 Acquired purpura fulminans (APF) associated with acute promyelocytic leukemia (APL)
42. #629 Comparison between horse antithymocyte globulin (ATG) alone and combined therapy (ATG, cyclosporine A, GM-CSF) for the treatment of children with severe aplastic anemia (SAA)
43. Phenotype–genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8and X‐chromosome inactivation
44. Deep vein thrombosis in a 13‐year‐old boy with hereditary protein S deficiency and a review of the pediatric literature
45. Impact of inherited thrombophilia on venous thromboembolism in children: a systematic review and meta-analysis of observational studies.
46. Phenotypic analysis of human BM T-cell depleted by soybean lectin agglutination and E rosetting with sheep RBC: relative enrichment of NK cells and a CD3 + ,CD2 -dim population.
47. Prothrombotic disorders in children with moyamoya syndrome.
48. 629 Comparison between horse antithymocyte globulin ATG alone and combined therapy ATG cyclosporine A GMCSF for the treatment of children with severe aplastic anemia SAA
49. Factor V Leiden Mutation in the Argentinian Population
50. Haemophilia B, severe childhood obesity and other extra-haematological features associated with similar 4Mb-deletions on Xq27: Clinical findings, molecular insights and literature update.
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