Tag Archive: Orphan Disease Center

Jan 12 2018

Birth Defects Awareness, Million Dollar Bike Ride Grant, WAO Center of Excellence, Alopecia and Thyroid Screening, New PolicyLab Video

The new year brings brand-new opportunities to advance pediatric research at Children’s Hospital of Philadelphia Research Institute, and if the first two weeks of 2018 are any indication, our investigators are off to a remarkable start. With January marking National Birth Defects Prevention Month, the Center for Fetal Diagnosis and Treatment at CHOP embarked on a campaign to raise awareness for birth defect treatments and research. Meanwhile, our friends at PolicyLab released an exciting video communicating their passionate mission to improve the well-being of children and families. This week, we also cover new pathways to discovery for conditions both rare and common, from hyperinsulinism to alopecia. If (like us), your new year’s resolution is to stay up to date with the latest CHOP research headlines, you’re in the right place!

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Dec 27 2017

Our Most Read Stories of 2017 Bring Back the Wonder of Childhood

It was a big year for children’s health: We celebrated the U.S. Food and Drug Administration’s approval of the world’s first chimeric antigen receptor (CAR)-T cell therapy this September, followed closely by approval of the very first gene therapy to treat inherited blindness this month — both of which have their roots at Children’s Hospital of Philadelphia and the University of Pennsylvania. But besides the big headline-making breakthroughs (brilliant as they are), we wanted to know what other stories captivated our readers in 2017.

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Jul 28 2017

Psychology in Media Award, Targeted Cancer Drugs, Dermatology App, CHOP ROP Model, Beckwith-Wiedemann Conference

CHOP Research In the NewsRead on for more exciting headlines from this week, including highlights from our inaugural “Deciphering Beckwith-Wiedemann Syndrome” conference.

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Jul 27 2017

CHOP Hosts Deciphering Beckwith-Wiedemann Syndrome Conference

kalish_cropIt was weekend of firsts on many fronts, as physicians, genetic counselors, nurses, researchers, and families gathered July 21–23 at Children’s Hospital of Philadelphia Research Institute for the inaugural Deciphering Beckwith-Wiedemann syndrome (BWS) conference. BWS is a rare overgrowth disorder involving genetic and epigenetic changes that occur approximately every one in 10,500 births.

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