Why Do We Still Need Vaccines?
Paul A. Offit, MD, explains why vaccines are still necessary even though vaccine-preventable diseases may not seem to be common.
Caring for your child
Search patient & family resources
Filter By
Type
Aggregated field
Topic
Showing 561 - 570 of 1583 results
How Do You Know Whether a Vaccine Has Been Tested Long Enough?
Paul A. Offit, MD, discusses at what point a vaccine has been studied enough in order to recommend its use. He talks specifically about the HPV vaccine.
Introduction of MRI: Basic Techniques and Protocols
A video presentation on Introduction of MRI: Basic Techniques and Protocols
Frequently Asked Questions about Gene Therapy for Hemophilia
Explore answers to the most common questions asked about gene therapy for hemophilia.
About Hemophilia
Hemophilia is a genetic disease that prevents blood from clotting properly leading to prolonged internal and external bleeding. Read more hemophilia and the existing treatments.
Gene Therapy in Hemophilia
View interactive webinars, educational resources and the latest news about hemophilia.
MitoAction
MitoAction’s mission is to improve the quality of life for children, adults, and families living with mitochondrial disease through support, education, outreach, advocacy and clinical research initiatives.
PALS (People Against Leigh Syndrome)
People Against Leigh Syndrome, (PALS), was formed in 2013 after William Martin, son of Neil and Lori Martin, was diagnosed with Leigh syndrome, a genetic neurometabolic disorder that can cause deterioration of the central nervous system, including the brain, spinal cord, and optic nerve.
The CHAMP Foundation
The Champ Foundation supports research toward better treatment and a cure for single large-scale mitochondrial deletion syndromes (SLSMDS), like Pearson syndrome.
Leigh Syndrome Parent Network: Facebook Support Group
This page is dedicated solely to the parents of children who have been diagnosed with Leigh's Syndrome - a mitochondrial disease.