773 results on '"Lambert, Michele P"'
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2. Transcription factor RUNX1 regulates coagulation factor XIII-A (F13A1): decreased platelet-megakaryocyte F13A1 expression and clot contraction in RUNX1 haplodeficiency
3. Genetic variants in canonical Wnt signaling pathway associated with pediatric immune thrombocytopenia
4. Hematologic and Immunologic Cases: Bone Marrow Failure
5. Hematologic and Immunologic Cases: Bleeding Disorder
6. Contributors
7. Hematologic and Immunologic Cases: Chronic Thrombocytopenia in a Child
8. Evaluating the clinical validity of genes related to hemostasis and thrombosis using the Clinical Genome Resource gene curation framework
9. Uncovering the Genetic Etiology of Inherited Bone Marrow Failure Syndromes Using a Custom-Designed Next-Generation Sequencing Panel
10. 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
11. Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome
12. Proceedings of the immune thrombocytopenia summit: new concepts in mechanisms, diagnosis, and management
13. Defective RAB31-mediated megakaryocytic early endosomal trafficking of VWF, EGFR, and M6PR in RUNX1 deficiency
14. An update on pediatric ITP: differentiating primary ITP, IPD, and PID
15. Hematologic abnormalities in Aicardi Goutières Syndrome
16. Distinct immune trajectories in patients with chromosome 22q11.2 deletion syndrome and immune-mediated diseases
17. Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel
18. Tapering thrombopoietin receptor agonists in primary immune thrombocytopenia: Expert consensus based on the RAND/UCLA modified Delphi panel method
19. Contributors
20. Hematologic and oncological manifestations of 22q11.2 deletion syndrome
21. Diagnostic Challenges in Pediatric Hemophagocytic Lymphohistiocytosis
22. Human mutational constraint as a tool to understand biology of rare and emerging bone marrow failure syndromes
23. Mini-clusters of postadenovirus VITT
24. Chapter 140 - Hemolytic Disease of the Fetus and Newborn
25. Chapter 139 - Anemia in the Newborn Infant
26. Hemolysis After Medication Exposure in Pediatric Patients With G6PD Deficiency
27. Hemolysis After Medication Exposure in Pediatric Patients With G6PD Deficiency
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. Inherited Platelet Disorders: A Modern Approach to Evaluation and Treatment
31. Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic disease
32. What is in a name: defining pediatric refractory ITP
33. Thromboelastography Changes of Whole Blood Compared to Blood Component Transfusion in Infant Craniosynostosis Surgery
34. Patients with common variable immunodeficiency with autoimmune cytopenias exhibit hyperplastic yet inefficient germinal center responses
35. 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
36. The Treatment of Immune Thrombocytopenia
37. AAV-8 and AAV-9 Vectors Cooperate with Serum Proteins Differently Than AAV-1 and AAV-6
38. Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes
39. Defective RAB1B-related megakaryocytic ER-to-Golgi transport in RUNX1 haplodeficiency: impact on von Willebrand factor
40. 2-O, 3-O desulfated heparin mitigates murine chemotherapy- and radiation-induced thrombocytopenia
41. Eltrombopag for use in children with immune thrombocytopenia
42. Platelet Transfusions
43. Special Disease Considerations in the Neonate
44. Evaluating the clinical validity of genes related to hemostasis and thrombosis using the ClinGen gene curation framework
45. Clinical updates in adult immune thrombocytopenia
46. Updates in diagnosis of the inherited platelet disorders
47. Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease
48. Coagulation Cascade and Fibrinolysis Pathway: Assessment in the Laboratory
49. A proposal for new definition (s) and management approach to paediatric refractory ITP: Reflections from the Intercontinental ITP Study Group
50. Chapter 104 - Congenital Thrombocytopenia
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