Glycogen storage disease - Wikipedia, the free encyclopedia
Glycogen storage disease (GSD, also glycogenosis and dextrinosis) is the result of defects in the processing of glycogen synthesis or breakdown within ...
http://en.wikipedia.org/wiki/Glycogen_storage_disease...
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Glycogen Storage Disease Type I -- GeneReviews -- NCBI Bookshelf
2 Sep 2008 ... Disease characteristics. Glycogen storage disease type I (GSDI) is characterized by accumulation of glycogen and fat in the liver and ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...
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Glycogen storage disease type I - Wikipedia, the free encyclopedia
Glycogen storage disease type I (GSD I) or von Gierke's disease, is the most common of the glycogen storage diseases. This genetic disease results from ...
http://en.wikipedia.org/wiki/Glycogen_storage_disease_type_I...
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OMIM - GLYCOGEN STORAGE DISEASE II
MIM #232300 · Text · Description · Clinical Features · Genotype/Phenotype Correlations · Pathogenesis · Diagnosis · Clinical Management · Inheritance ...
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=232300...
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Disorders of Carbohydrate Metabolism: Hereditary Metabolic ...
Glycogen storage diseases occur when there is a defect in the enzymes that are involved in the metabolism of ...
http://www.merck.com/mmhe/sec23/ch282/ch282b.html...
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Glycogen Storage Disease Type II (Pompe Disease) -- GeneReviews ...
5 Aug 2008 ... Disease characteristics. Glycogen storage disease type II (GSD II), or Pompe disease, is classified by age of onset, organ involvement, ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...
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Glycogen storage disease type II - Wikipedia, the free encyclopedia
Glycogen storage disease type II (also called Pompe disease or acid maltase deficiency) is a neuromuscular, autosomal recessive metabolic disorder in the
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http://en.wikipedia.org/wiki/Glycogen_storage_disease_type_I...
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Glycogen Storage Disease Type V -- GeneReviews -- NCBI Bookshelf
12 May 2009 ... Disease characteristics. Glycogen storage disease type V (GSDV, McArdle disease) is a metabolic myopathy characterized by exercise ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...
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Glycogen storage disease type V - Wikipedia, the free encyclopedia
Glycogen storage disease type V (GSD-V) is a metabolic disorder, more specifically a glycogen storage disease, caused by a deficiency of
myophosphorylase. ...
http://en.wikipedia.org/wiki/Glycogen_storage_disease_type_V...
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OMIM - GLYCOGEN STORAGE DISEASE III
MIM #232400 · Text · Description · Clinical Features · Biochemical Features · Diagnosis · Molecular Genetics · Population Genetics ...
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=232400...
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