799 results on '"Lambert, Michele"'
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2. Hematologic and Immunologic Cases: Bleeding Disorder
3. Contributors
4. Hematologic and Immunologic Cases: Chronic Thrombocytopenia in a Child
5. Genetic variants in canonical Wnt signaling pathway associated with pediatric immune thrombocytopenia
6. Uncovering the Genetic Etiology of Inherited Bone Marrow Failure Syndromes Using a Custom-Designed Next-Generation Sequencing Panel
7. Evaluating the clinical validity of genes related to hemostasis and thrombosis using the Clinical Genome Resource gene curation framework
8. Serum cytokine panels in pediatric clinical practice
9. Association of laboratory test results with the bleeding history in patients with inherited platelet function disorders (the Bleeding Assesment Tool - LABoratory tests substudy): communication from the Platelet Physiology ISTH-SSC
10. Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome
11. Proceedings of the immune thrombocytopenia summit: new concepts in mechanisms, diagnosis, and management
12. Defective RAB31-mediated megakaryocytic early endosomal trafficking of VWF, EGFR, and M6PR in RUNX1 deficiency
13. An update on pediatric ITP: differentiating primary ITP, IPD, and PID
14. Ras‐associated autoimmune lymphoproliferative disorder.
15. Contributors
16. Hematologic and oncological manifestations of 22q11.2 deletion syndrome
17. What is in a name: defining pediatric refractory ITP
18. Diagnostic Challenges in Pediatric Hemophagocytic Lymphohistiocytosis
19. Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel
20. Tapering thrombopoietin receptor agonists in primary immune thrombocytopenia: Expert consensus based on the RAND/UCLA modified Delphi panel method
21. Evidence of thrombotic microangiopathy in children with SARS-CoV-2 across the spectrum of clinical presentations
22. Human mutational constraint as a tool to understand biology of rare and emerging bone marrow failure syndromes
23. Illustrated State‐of‐the‐Art Capsules of the ISTH 2020 Congress
24. Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC
25. Hemolysis After Medication Exposure in Pediatric Patients With G6PD Deficiency
26. Transcription Factor NRF2 is Activated by Erythrophagocytosis of Oxidized Red Blood Cell Products and Suppresses the IL-12-IFNg-IL-10 Axis in a Murine Model of Hyperinflammatory Disease
27. Association of laboratory test results with the bleeding history in patients with inherited platelet function disorders (the BAT-LAB substudy): communication from the Platelet Physiology ISTH-SSC
28. Proteomic profiling of MIS-C patients indicates heterogeneity relating to interferon gamma dysregulation and vascular endothelial dysfunction
29. Common variable immunodeficiency–associated endotoxemia promotes early commitment to the T follicular lineage
30. Hemolysis After Medication Exposure in Pediatric Patients With G6PD Deficiency
31. Multisystem inflammatory syndrome in children and COVID-19 are distinct presentations of SARS-CoV-2
32. The Treatment of Immune Thrombocytopenia
33. Thromboelastography Changes of Whole Blood Compared to Blood Component Transfusion in Infant Craniosynostosis Surgery
34. Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic disease
35. Patients with common variable immunodeficiency with autoimmune cytopenias exhibit hyperplastic yet inefficient germinal center responses
36. Chapter 140 - Hemolytic Disease of the Fetus and Newborn
37. Chapter 139 - Anemia in the Newborn Infant
38. Evaluating the clinical validity of genes related to hemostasis and thrombosis using the ClinGen gene curation framework
39. Emapalumab for the treatment of refractory cytokine release syndrome in pediatric patients
40. Platelet Transfusions
41. Special Disease Considerations in the Neonate
42. A proposal for new definition (s) and management approach to paediatric refractory ITP: Reflections from the Intercontinental ITP Study Group
43. HTRS2023.P1.1 Comparison of light transmission and whole blood lumiaggregometry in evaluation of pediatric patients for platelet function disorders
44. Coagulation Cascade and Fibrinolysis Pathway: Assessment in the Laboratory
45. Clinical updates in adult immune thrombocytopenia
46. A case-control study of bleeding risk in children with 22q11.2 deletion syndrome undergoing cardiac surgery.
47. Case 11.9.5 - Hematologic and Immunologic Cases: Bone Marrow Failure
48. Case 11.9.3 - Hematologic and Immunologic Cases: Chronic Thrombocytopenia in a Child
49. Case 11.9.1 - Hematologic and Immunologic Cases: Bleeding Disorder
50. Sports participation in chronic immune thrombocytopenia: Safer than you thought?
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