CHOP Hosts Annual Prom for Patients and Families
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Earlier this month, Children’s Hospital of Philadelphia (CHOP) was excited to host the annual Joshua Kahan Fund Prom at CHOP for patients and their families.
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Earlier this month, Children’s Hospital of Philadelphia (CHOP) was excited to host the annual Joshua Kahan Fund Prom at CHOP for patients and their families.
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A look back at the last five decades of treatment options to what lies ahead with additional potentially curative gene therapies.
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Yesterday, more than 3,000 people gathered at the Philadelphia Zoo to celebrate the 27th Children’s Hospital of Philadelphia (CHOP) Fetal Family Reunion, representing patients and families from across the country.
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Researchers from Children’s Hospital of Philadelphia (CHOP) confirmed that “mini-intestines” generated from patient tissue samples and grown in a lab can accurately replicate certain features of Crohn’s disease, which will allow them to study the epithelium, the thin layer of cells lining the intestine, that is broken down in patients with inflammatory bowel disease.
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The study captured genetic variants at extremely low levels, and dozens of patients began new therapies as a result of the findings.
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Collaboration among CHOP, Alex’s Lemonade Stand Foundation, the Pacific Pediatric Neuro-Oncology Consortium, and Children’s Brain Tumor Network paves the way for new collaborative models to accelerate discoveries.
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Dr. Eric Eichenwald, CHOP’s Division Chief of Neonatology, co-authored the first national standards for neonatal care published by the American Academy of Pediatrics (AAP).
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CHOP researchers have shown that IgA acts as a “tuner” that regulates the number of microbes the body sees every day, restraining a systemic immune response.
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While OTC Hearing Aids may seem like an attractive and affordable option for children with hearing loss, caregivers need to be cautious when seeking appropriate amplification for their children.
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CHOP researchers will develop gene therapies for multiple sulfatase deficiency, a devastating lysosomal storage disorder, with the goal of first-in-human trials.