Content related to A Team of Their Own
Growing New Leaders in Pediatric Pulmonology
November 4, 2021
Under a $1.5 million federal grant, Children’s Hospital Los Angeles is investing in innovative interdisciplinary leadership education in the field.
Physical, Mental Symptoms Co-Occur
September 6, 2016
Researchers at the Institute for the Developing Mind at Children’s Hospital Los Angeles have analyzed current gene-disease findings to understand why people with neurodevelopmental and mental illness
Children’s Hospital Los Angeles Awarded $24.5 Million to Establish a Center Addressing Chronic Health Disparities in Latino/a/x Children and Families
October 19, 2021
The new center will address health concerns that disproportionately affect the Latino/a/x community in Southern California.
Protons vs. Photons: One Letter Could Make a Big Difference in Brain Tumors
March 2, 2016
Medulloblastoma, the most common malignant brain tumor occurring in children, is a fast-growing cancer that affects nearly 2 million people – including adults – annually. Traditionally
Statement by President and CEO Paul S. Viviano on the passing of Morton M. Woolley, MD
January 13, 2020
Dr. Morton M. Woolley was a beloved surgeon, professor, pioneer and leader at Children's Hospital Los Angeles from 1960 until his retirement in 1992, who held a worldwide reputation for surgical
Researchers Awarded $3.5 Million to Study Brain and Cranium Development in Children
September 28, 2021
Children’s Hospital Los Angeles and Children’s National Hospital collaborate, creating the first ever toolbox to help clinicians understand how the brain and cranium grow together.
Symptoms, Treatment and Prevention of Type 1 Diabetes
July 13, 2015
How do you know if your child has Type 1 diabetes? How is it treated? And how can Type 2 diabetes be prevented? Our expert weighs in.
Management of Sickle Cell Disease: A Perspective for Pediatricians
March 3, 2020
Sickle cell disease (SCD) is one of the most common genetic blood disorders, affecting over 100,000 Americans and 1 in 365 African-American newborn babies. It is an autosomal recessive condition
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