An $8 million gift from the Foundation of Caring will help CHOC advance research for a rare lysosomal storage disorder, Pompe Disease.
CHOC Resident Follows in His Father’s Footsteps
Dr. Tim Hicks jokingly calls himself “Hicks 2.0,” a proud nod to his CHOC pulmonologist father, Dr. David Hicks.
William, Jeff and Jennifer Gross Family Foundation donates $2 million to CHOC’s Neonatal Intensive Care Unit
The recent gift rounds the Foundation’s support of CHOC’s neonatal services to $7 million in the past 12 months.
CHOC performs first in-human gene therapy dosing for MPS I
CHOC clinicians recently administered the first ever in-human dosing of gene therapy for Hurler Syndrome, a rare lysosomal storage disease.
Journey to a rare diagnosis: Colten’s story
A CHOC PICU nurse tells the story of her son, Colten, who received a rare Alström Syndrome diagnosis with the help of specialists at CHOC.
How CHOC otolaryngologists are changing tonsillectomy recovery
Two CHOC otolaryngologists are championing intracapsular tonsillectomies to reduce bleeding and hospital readmission rates.
