3rd Annual Mitochondrial Medicine Education Day
The 3rd annual Mitochondrial Medicine Virtual Symposium and Education Day will explore recent advances in mitochondrial DNA disease recurrent prevention, genetic diagnostic testing, acute care…
The 3rd annual Mitochondrial Medicine Virtual Symposium and Education Day will explore recent advances in mitochondrial DNA disease recurrent prevention, genetic diagnostic testing, acute care…
Primary mitochondrial diseases share in common an impaired ability to generate energy. Highly heterogeneous in etiology and phenotypes, primary mitochondrial diseases are collectively the most…
Katharine Press Callahan, MD, is a neonatology fellow at Children’s Hospital of Philadelphia. Her research focuses on how neonatologists use genetic information to make medical…
Katherine Szigety, MD, PhD completed her MD-PhD training at the Perelman School of Medicine at the University of Pennsylvania. Her thesis work in Biochemistry and…
Dr. Ralph DeBerardinis, MD, PhD joined the faculty of UT Southwestern Medical Center in 2008 and joined the Children’s Medical Center Research Institute at UTSW…
At the end of this session, learners will be able to understand the genetic basis of childhood epilepsies, to learn about the potential for precision…
At the end of this session, learners will be able to gain an overview of genetic diagnostic advances and its therapeutic implications in neuromuscular diseases,…
Turner syndrome is a genetic disorder that affects girls and results in a variety of health problems ranging from short stature and lack of pubertal…
Our mitochondria make the energy that keeps us alive. Geneticist Marni Falk, MD, joins Madeline to discuss what happens when our mitochondria don’t work properly,…
World-renowned hematologist and scientist Dr. Katherine High has spent much of her career focused on achieving a goal few believed was possible: developing gene therapies…