HIE Registry Webinar

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This webinar describes the collaborative effort to build a registry for hypoxic ischemic encephalopathy (HIE). The CP Research Network has teamed up with Hope for HIE and the Newborn Brain Society to build extensions to the CP Research Network registries to support the long term study of people affected by HIE. Dr. Danielle Guez Barber, principal investigator for the HIE Registry project and Betsy Pilon, Executive Director of Hope for HIE, join CP Research Network CEO Paul Gross to discuss the development and importance of an HIE Registry.

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