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Results for Inherited Thrombocytopenia

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Michele Lambert, MD, MSTR
Michele Lambert

Dr. Lambert's research focuses on understanding the mechanisms of inherited and acquired thrombocytopenia in pediatric patients. Using clinical translational methods to link discovery in rare platelet disorders with optimizing next-generation sequencing for clinical practice, she has been involved in the Undiagnosed Disease Network Program and the Frontier Program in Immune Dysregulation, incorporating genetics of platelet disorders and immunohematology.

E-mail:
lambertm [at] chop.edu
Julia T. Warren, MD, PhD
Julia T. Warren

Dr. Warren studies normal and aberrant hematopoiesis, with a special interest in granulopoiesis. Her research aims to understand the pathogenesis of severe congenital neutropenia and its risk for malignant transformation. She has a clinical interest in neutropenia syndromes including clinical trials.

E-mail:
warrenjt [at] chop.edu

Targeting Abnormal Signals Suggests Novel Method to Treat a Rare Childhood Blood Disease

Published on
Oct 9, 2018
in Press Releases
In Animal Study, CHOP Hematologist Restores Blood Cell Function in Fanconi Anemia

Diversity Makes a Difference: Q&A With Brian Estevez, PhD, New Diversity Fellow

Published on
Jan 25, 2017
in Cornerstone Blog
Brian Estevez, PhD
Looking at a scientific problem from new and different perspectives is what research is all about, which is why Children's Hospital of Philadelphia's Research Institute is dedicated to cultivating a more diverse workforce. "We value diversity within our research community and it is undoubtedly part of what makes us successful," wrote Bryan A. Wolf, MD, PhD, Chief Scientific Officer and Director
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  • Principal Investigator / Faculty (2)

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  • Office of Academic Training and Outreach Programs (1)
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