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Planning for Holiday Gatherings When Your Child Has a Food Allergy
Find expert advice from CHOP clinical dietitians on how to plan an inclusive — and safe — holiday gatherings.
Make the Diagnosis: Fall 2018
A 24-month-old African-American boy was admitted to the ER after abnormal hemoglobin results. Exam was notable for pallor and a 2/6 systolic ejection murmur, with no jaundice or hepatosplenomegaly. White blood cell differential analysis showed 14% neutrophils, 84% lymphocytes, 2% atypical lymphocytes, and calculated absolute neutrophil count of 520 per uL.
CHOP Scientists Report How Some Cancer Cells Develop Resistance to CAR T-cell Therapy
CHOP researchers analyze how some cancer cells resist a groundbreaking cellular therapy, and have found clues to overcoming that resistance.
Children’s Doctor News and Updates: Fall 2018
Read the latest news from CHOP, including the results of three research studies: baby monitors, button batteries and honey, and cell phone use. Meet our new Cardiothoracic Surgery Chief and browse our latest clinical pathways.
CHOP Wins Pediatric Excellence Award
The award recognizes a hospital or unit that has demonstrated an unwavering commitment to the delivery of pediatric care.
CHOP Expert Featured in MetroKids
Erica Schindewolf, a genetic counselor in the CFDT, weighs in on what patients should know about genetic screening tests during pregnancy.
Working to Improve Cure Rates for High-risk Neuroblastoma
Researchers at CHOP are working to discover the fundamental mechanisms that subvert normal neural development and orchestrate neuroblastoma tumorigenesis, and then to translate this knowledge into more effective and less toxic therapies.
CHOP-Penn Receive 22q11.2 Society Inaugural Special Service Award
CHOP and Penn were honored for outstanding, long-standing, exemplary and unwavering commitment and contributions to the chromosome 22q11.2 community since 1992.
Everything Parents Need to Know about AFM
Parents magazine interviewed a CHOP expert about signs of acute flaccid myelitis (AFM), the polio-like illness that can cause lifelong paralysis.
Ashkenazi Jewish Founder Mutation Identified in Leigh Syndrome
Decades after two brothers died from a mitochondrial disease, scientists identified the causative gene mutation and say the mutation should be added to carrier screening programs.