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Vaccine News & Notes — April 2023

Get details about the Hilleman essay contest for students in grades 6 through 12, and review the science on two "controversies" surrounding COVID-19: masks and lab leak.

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Two Focal Lesions: Extra Rare Cases Not so Rare at CHOP

The Congenital Hyperinsulinism Center at Children’s Hospital of Philadelphia, with a high volume of approximately 80 congenital hyperinsulinism (HI) cases a year, sees a large share of unusual cases.

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Neurodevelopmental Outcomes in HI

Unrecognized or inadequately treated hyperinsulinism (HI) poses a high risk of adverse neurodevelopmental outcomes due to the combined insult of hypoglycemia and lack of alternate brain fuels.

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When Hyperinsulinism is a Family Affair

Inactivating mutations in the beta cell KATP channels are the most common cause of congenital hyperinsulinism (HI), accounting for approximately 60% of all cases with known genotype. The beta cell KATP channels play a very important role in the regulation of insulin secretion by coupling the metabolic state of the cell to membrane potential.

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A Day in the Life

Anne Ades, MD, MSEd, serves as Medical Co-Director of CHOP’s Center for Simulation, Advanced Education and Innovation, which uses computerized medical manikins to teach medical procedures. This is a day in her life.

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The Flame of Discovery Burns Brightly

For 22 years, collaborative research at CHOP’s Biesecker Pediatric Liver Center has been changing the future for children with serious liver diseases.

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