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1. Serum cytokine panels in pediatric clinical practice

3. Genetic variants in canonical Wnt signaling pathway associated with pediatric immune thrombocytopenia

6. Contributors

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

15. Hematologic abnormalities in Aicardi Goutières Syndrome

17. Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel

19. Contributors

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

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

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

38. Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

42. Platelet Transfusions

44. Evaluating the clinical validity of genes related to hemostasis and thrombosis using the ClinGen gene curation framework

47. Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

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