Thanks to a collaboration between Columbia and Cornell doctors, Yasin Samad is one of the first children in the United States to receive an innovative artificial heart valve.
Joey, a lightweight sensing fabric designed by Columbia engineers, can be worn by caregivers to monitor Kangaroo Mother Care practices with their babies.
A novel omega-3 injectable emulsion reduces brain damage in newborn rodents experiencing lack of oxygen at delivery, a major cause of disability in human infants and children.
A new program at Columbia is working to equip the next generation of pediatricians with the skills to address common mental health concerns in their patients.
Children were spared the worst of COVID-19 early on, but they are now suffering psychological consequences from the pandemic’s social upheaval. Here’s what parents and educators can do.
New insights by Columbia researchers into MIS-C, a rare but serious complication of COVID in children, may lead to faster diagnosis and better treatment.
Columbia researchers could receive up to $9.4 million to learn about long COVID in children and young adults as part of NIH’s REsearching COVID to Enhance Recovery (RECOVER) initiative.
Getting a baby on an overnight sleep schedule can seem like an impossible dream. But it can be achieved in three days. And you can start tonight. The only obstacle is you.
Babies born during the pandemic’s first year—even to moms who did not have COVID during pregnancy—scored slightly lower on a screening test of social and motor skills compared to pre-pandemic babies.
Alusine and Isatu Jalloh traveled 4,300 miles to give their girls a chance for a better life. At Morgan Stanley Children's Hospital, a team of Columbia surgeons successfully separated the twins.
When Emma was diagnosed with type 1 diabetes at age 10, she worried she would have to give up dance. But her team at Columbia's Naomi Berrie Diabetes Center has kept her on her toes.
Columbia University Irving Medical Center has been selected by the National Organization for Rare Disorders to join a national network aimed at improving patient care for people with rare diseases.