Media Summary: Approximately one in 10 Americans suffer from a rare Shaylee isn't your average seventeen-year-old and it's not just the fact that she has Duke research gives hope to patients with

Behind The Mystery Pompe Disease - Detailed Analysis & Overview

Approximately one in 10 Americans suffer from a rare Shaylee isn't your average seventeen-year-old and it's not just the fact that she has Duke research gives hope to patients with Four-year-old Luke Barriger was diagnosed two years ago with Kare Anstett, MS, CGS, from NYU Langone Health gives her presentation on Genetics of Pope Raymond speaks about when he was first diagnosed and how you can help others living with rare

Priya Kishnani, MD, professor of Pediatrics at Duke University School of Medicine and practicing geneticist at Duke Children's ... Stephanie Austin of Duke Medical Center talks about the genetics of infantile, juvenile, and late-onset Priya Kishnani, MD, Chief, Division of Medical Genetics and Professor of Pediatrics at the Duke University School of Medicine, ... Heather A. Lau, MD, Director, Lysosomal Storage Disease Program at NYU Langone in New York City discusses When two-year medical student, Paul McIntosh, was diagnosed with late-onset

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Behind the Mystery: Pompe Disease
The Balancing Act Goes Behind the Mystery
The Pathophysiology of Pompe Disease
Understanding Pompe Disease: My Journey with Glycogen Storage
Sanofi – Living With Pompe Disease – Shaylee’s Story
Duke research gives hope to patients with Pompe Disease
Impact the World: Pompe Disease | Michigan State
Shaylee’s Story: Journey Ahead Program (Pompe Disease)
Genetics of Pompe Disease
Fair For Rare: How you can help Raymond and others with Pompe Disease
What is Pompe Disease?
Late-onset Pompe Disease - Patient's Story
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Behind the Mystery: Pompe Disease

Behind the Mystery: Pompe Disease

Approximately one in 10 Americans suffer from a rare

The Balancing Act Goes Behind the Mystery

The Balancing Act Goes Behind the Mystery

On today's show,The Balancing Act goes

Sponsored
The Pathophysiology of Pompe Disease

The Pathophysiology of Pompe Disease

Pompe disease

Understanding Pompe Disease: My Journey with Glycogen Storage

Understanding Pompe Disease: My Journey with Glycogen Storage

Join us as we explore

Sanofi – Living With Pompe Disease – Shaylee’s Story

Sanofi – Living With Pompe Disease – Shaylee’s Story

Shaylee isn't your average seventeen-year-old and it's not just the fact that she has

Sponsored
Duke research gives hope to patients with Pompe Disease

Duke research gives hope to patients with Pompe Disease

Duke research gives hope to patients with

Impact the World: Pompe Disease | Michigan State

Impact the World: Pompe Disease | Michigan State

Four-year-old Luke Barriger was diagnosed two years ago with

Shaylee’s Story: Journey Ahead Program (Pompe Disease)

Shaylee’s Story: Journey Ahead Program (Pompe Disease)

Shaylee has been living with

Genetics of Pompe Disease

Genetics of Pompe Disease

Kare Anstett, MS, CGS, from NYU Langone Health gives her presentation on Genetics of Pope

Fair For Rare: How you can help Raymond and others with Pompe Disease

Fair For Rare: How you can help Raymond and others with Pompe Disease

Raymond speaks about when he was first diagnosed and how you can help others living with rare

What is Pompe Disease?

What is Pompe Disease?

Understanding

Late-onset Pompe Disease - Patient's Story

Late-onset Pompe Disease - Patient's Story

Brad Crittendale is a typical late-onset

Dr Kishnani Describes Pompe Disease

Dr Kishnani Describes Pompe Disease

Priya Kishnani, MD, professor of Pediatrics at Duke University School of Medicine and practicing geneticist at Duke Children's ...

The Genetics of Pompe Disease

The Genetics of Pompe Disease

Stephanie Austin of Duke Medical Center talks about the genetics of infantile, juvenile, and late-onset

How Duke University Has Led Pompe Disease Research

How Duke University Has Led Pompe Disease Research

Priya Kishnani, MD, Chief, Division of Medical Genetics and Professor of Pediatrics at the Duke University School of Medicine, ...

Pompe Day highlights those who live with rare genetic condition

Pompe Day highlights those who live with rare genetic condition

Mary Joyce lives with the rare

Pompe Disease: Overview, Diagnosis Challenges, Treatments, and Emerging Therapies

Pompe Disease: Overview, Diagnosis Challenges, Treatments, and Emerging Therapies

Heather A. Lau, MD, Director, Lysosomal Storage Disease Program at NYU Langone in New York City discusses

For Boy With Pompe Disease, Every Active Day Is a Gift (Jane Emerson, MD)

For Boy With Pompe Disease, Every Active Day Is a Gift (Jane Emerson, MD)

William Lyons has

Late Onset Pompe Disease - A Patient's Marathon to Diagnosis

Late Onset Pompe Disease - A Patient's Marathon to Diagnosis

When two-year medical student, Paul McIntosh, was diagnosed with late-onset

Physical Therapy and Pompe Disease

Physical Therapy and Pompe Disease

During Duke's annual late-onset