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  1. Pompe disease: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/condition/pompe-disease
    ... but they typically do not show signs and symptoms of the condition. Other Names for This Condition Acid maltase deficiency Acid maltase deficiency disease Alpha-1,4-glucosidase ...
  2. TK2-Related Mitochondrial DNA Maintenance Defect, Myopathic Form - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK114628
    ... hypertrophic cardiomyopathy. The diagnosis is based on complete deficiency of activity of the ... Following Initial Diagnosis To establish the extent of disease and needs ...
  3. Conclusions From Draft Comparative Effectiveness Review of HSCT - Future Research Needs for Hematopoietic Stem-Cell ... 
    https://www.ncbi.nlm.nih.gov/books/NBK84479
    ... s disease, β-mannosidosis, mucolipidosis III or IV, glycogen storage disease type II ... HSCT compared with symptom management or disease natural history. All five patients ...
  4. xmlghr-summaries.xml 
    https://medlineplus.gov/download/ghr-summaries.xml
    ... maltase</synonym><synonym >Lysosomal glycogen storage disease without acid maltase deficiency</synonym><synonym >X-linked pseudoglycogenosis II</synonym><synonym > ...
  5. xmlTopicIndex.xml 
    https://medlineplus.gov/download/TopicIndex.xml
    ... name><other_name >Lysosomal glycogen storage disease without acid maltase deficiency</other_name><other_name >X-linked pseudoglycogenosis II</ ...
  6. Genetic Conditions 
    https://medlineplus.gov/genetics/condition
    ... Acid lipase deficiency, see Lysosomal acid lipase deficiency Acid maltase deficiency, see Pompe disease Acid maltase deficiency disease, see Pompe disease ACLS, see Acrocallosal syndrome ...
  7. Findings - Enzyme-Replacement Therapies for Lysosomal Storage Diseases - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK117223
    ... for the treatment of Type 1 Gaucher disease. Glycogen Storage Disease type II (Pompe Disease) Eight studies of alglucosidase alfa as treatment for glycogen storage disease type II (Pompe disease) are summarized in Table 10 . 72 – ...
  8. Danon disease: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/condition/danon-disease
    ... normal acid maltase Lysosomal glycogen storage disease without acid maltase deficiency X-linked pseudoglycogenosis II X-linked vacuolar cardiomyopathy ...
  9. Genetic Conditions: L 
    https://medlineplus.gov/genetics/condition-l
    ... see Danon disease Lysosomal glycogen storage disease without acid maltase deficiency, see Danon disease Lysosomal protective protein deficiency, see ...
  10. Resource Bibliography - Enzyme-Replacement Therapies for Lysosomal Storage Diseases - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK117228
    ... et al. Progress in enzyme replacement therapy in glycogen storage disease type II. Therapeutic Advances in Neurological Disorders. 2009; 2 (3): ... therapy on five patients with advanced late-onset glycogen storage disease type II: a 2-year follow-up study. J Inherit ...
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