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Bhupesh Sangrur, IN
greathealthinspired California
I am former Pharmaeutical Rep that worked in the areas of Alz., Heart Disease & Mental... More

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Genetics Home Reference: glycogen storage disease type V by nih.gov Reviewed July 2010 What is glycogen storage disease type V? Glycogen storage disease type V... such as poor stamina; others do not experience any symptoms. How common is glycogen storage disease...
Genetics Home Reference: glycogen storage disease type III by nih.gov September 2010 What is glycogen storage disease type III? Glycogen storage disease... is glycogen storage disease type III? The incidence of GSDIII in the United States is 1 in 100,000...
Genetics Home Reference: glycogen storage disease type VI by nih.gov September 2010 What is glycogen storage disease type VI? Glycogen storage disease type VI... have any related health problems. How common is glycogen storage disease type VI? The exact...
Genetics Home Reference: glycogen storage disease type IX by nih.gov  definitions Reviewed September 2012 What is glycogen storage disease type IX? Glycogen... are usually mild. How common is glycogen storage disease type IX? GSD IX that affects the liver...
Genetics Home Reference: glycogen storage disease type IV by nih.gov Reviewed February 2013 What is glycogen storage disease type IV? Glycogen storage disease... is glycogen storage disease type IV? GSD IV is estimated to occur in 1 in 600,000 to 800,000 individuals...
Genetics Home Reference: glycogen storage disease type 0 by nih.gov Reviewed January 2014 What is glycogen storage disease type 0? Glycogen storage disease... they can include developmental delay and growth failure. How common is glycogen storage disease type 0...
Genetics Home Reference: glycogen storage disease type VII by nih.gov Reviewed April 2014 What is glycogen storage disease type VII? Glycogen storage disease... or weakness related to the disorder. How common is glycogen storage disease type VII...
Modulating Autophagy as a Treatment for Lysosomal Storage Diseases by nih.gov of lysosomal storage diseases by inhibition of autophagy. Pompe disease is an example of a genetic lysosomal storage disease caused by a reduction or absence of acid alpha-glucosidase (GAA). Patients with Pompe...
Alpha-Glucosidase Chaperones and Inhibitors for Treatment of Pompe Disease and Type 2 Diabetes by nih.gov that can act as chaperones and correct the misfolding of mutated alpha-glucosidase enzyme. Pompe disease... disease is enzyme replacement, which in this case costs approximately $300,000 per year and elicits...
Genetics Home Reference: Danon disease by nih.gov What other names do people use for Danon disease? glycogen storage disease type 2B glycogen storage disease type IIb lysosomal glycogen storage disease with normal acid maltase For more information...

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Facts ... toring food: Most products have storage instructions on the label its important to follow these ... » Read on
Prevention ... sure that chopping boards are washed and dried properly before storage to reduce the risk of bacteria growing, ... » Read on