About Pompe Disease - SaveChloe
Late-onset Pompe disease in a 54 year-old sportsman with an episode of syncope- a case report
Glycogen Storage Diseases Presenting as Hypertrophic Cardiomyopathy | NEJM
JCM | Free Full-Text | The Value of Cardiac Magnetic Resonance Imaging in Identification of Rare Diseases Mimicking Hypertrophic Cardiomyopathy
Giant Heart of Classical Infantile-Onset Pompe Disease With Mirror Image Dextrocardia | Circulation: Cardiovascular Imaging
Correction of oxidative stress enhances enzyme replacement therapy in Pompe disease | EMBO Molecular Medicine
Pompe Disease
Pompe Disease: Presentation and Management of Early Onset Type with Perioperative Considerations | Insight Medical Publishing
Pattern and prognostic value of cardiac involvement in patients with late-onset pompe disease: a comprehensive cardiovascular magnetic resonance approach | Journal of Cardiovascular Magnetic Resonance | Full Text
Pathophysiology of late-onset Pompe disease. Abbreviations: GAA, acid... | Download Scientific Diagram
Pattern and prognostic value of cardiac involvement in patients with late-onset pompe disease: a comprehensive cardiovascular magnetic resonance approach | Journal of Cardiovascular Magnetic Resonance | Full Text
![PDF] The infantile-onset form of Pompe disease: an autopsy diagnosis | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/5650831eafb2c4380f4c63b62c9b7d061055fbf2/3-Figure2-1.png "PDF] The infantile-onset form of Pompe disease: an autopsy diagnosis | Semantic Scholar")
PDF] The infantile-onset form of Pompe disease: an autopsy diagnosis | Semantic Scholar
Rescue of Advanced Pompe Disease in Mice with Hepatic Expression of Secretable Acid α-Glucosidase - ScienceDirect
Therapeutic Benefit of Autophagy Modulation in Pompe Disease: Molecular Therapy
Late-onset Pompe Patients Have Low Heart Disease Risk, Study Finds
Characterization of pre- and post-treatment pathology after enzyme replacement therapy for pompe disease | Laboratory Investigation
Pompe Disease: Presentation and Management of Early Onset Type with Perioperative Considerations | Insight Medical Publishing
Non-specificity of symptoms in infantile-onset Pompe disease may delay the diagnosis and institution of treatment | BMJ Case Reports
About Pompe Disease - SaveChloe
Pompe Disease: Causes, Symptoms, and Treatment | LSDSS India
Biomolecules | Free Full-Text | Pompe Disease: New Developments in an Old Lysosomal Storage Disorder
Pompe Disease: Causes Types Symptoms Signs Diagnosis Treatment FAQs
Pompe Disease (also called Glycogen storage disease type 2) | CheckRare
![PDF] Towards a molecular therapy for glycogen storage disease type II (Pompe disease). | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/23096233713bb3c15c35b98768f1ecd3d20e276c/4-Figure3-1.png "PDF] Towards a molecular therapy for glycogen storage disease type II (Pompe disease). | Semantic Scholar")
PDF] Towards a molecular therapy for glycogen storage disease type II (Pompe disease). | Semantic Scholar
Frontiers | Case Report: Identification of Compound Heterozygous Mutations in a Patient With Late-Onset Glycogen Storage Disease Type II (Pompe Disease )
Electrocardiogram in a patient with Pompe disease. Prominent R waves,... | Download Scientific Diagram
