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  1. 1
    History of glycogen storage disease type Ⅱ
    by Cheng ZHANG, Liang WANG
    Published 2018-08-01
    Subjects: “...Glycogen storage disease type Ⅱ...”
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    Article
  2. 2
    Progress in genetic diagnosis and management of glycogen storage disease typeⅡ
    by Cheng ZHANG, Juan YANG
    Published 2014-05-01
    Subjects: “...Glycogen storage disease typeⅡ...”
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    Article
  3. 3
    Clinical features and genetic analysis of 7 patients with late-onset glycogen storage disease typeⅡ
    Subjects: “...Glycogen storage disease type Ⅱ...”
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  4. 4
    Late-onset Pompe disease: what is the prevalence of limb-girdle muscular weakness presentation?
    Subjects: “...glycogen storage disease type II...”
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  5. 5
    Clinical efficacy of Myozyme on one ventilator dependent patient with late-onset glycogen storage disease typeⅡ
    Subjects: “...Glycogen storage disease type Ⅱ...”
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  6. 6
    Clinical study of respiratory function in patients with late-onset glycogen storage disease typeⅡ
    Subjects: “...Glycogen storage disease typeⅡ...”
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  7. 7
    Insight into "Consensus recommendations for diagnosis and treatment of glycogen storage disease typeⅡ"
    by Hong-zhi GUAN, Li-ying CUI
    Published 2014-05-01
    Subjects: “...Glycogen storage disease type Ⅱ...”
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    Article
  8. 8
    Pompe disease, a storage cardiomyopathy
    by Tiziana Felice
    Published 2017-10-01
    Subjects: “...glycogen storage disease type II...”
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    Article
  9. 9
    The infantile-onset form of Pompe disease: an autopsy diagnosis
    by Otávio César Cruz dos Santos
    Published 2015-12-01
    Subjects: “...Glycogen Storage Disease Type II...”
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    Article
  10. 10
    Current pharmacotherapy and diagnostic methods of Pompe Disease in Poland
    Subjects: “...glycogen storage disease type ii...”
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    Article
  11. 11
    Uptake of moss‐derived human recombinant GAA in Gaa−/− mice
    Subjects: “...glycogen storage disease type II...”
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  12. 12
    Novel GAA Variants and Mosaicism in Pompe Disease Identified by Extended Analyses of Patients with an Incomplete DNA Diagnosis
    Subjects: “...glycogen storage disease type II...”
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    Article
  13. 13
    Moss-Derived Human Recombinant GAA Provides an Optimized Enzyme Uptake in Differentiated Human Muscle Cells of Pompe Disease
    Subjects: “...glycogen storage disease type II...”
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    Article
  14. 14
    Identification of Seven Novel Mutations in the Acid Alpha-glucosidase Gene in Five Chinese Patients with Late-onset Pompe Disease
    Subjects: “...Alpha-glucosidase; DNA Mutational Analysis; Genetic Heterogeneity; Glycogen Storage Disease Type II...”
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    Article
  15. 15
    Countermeasures of six difficult-to-wean patients with severe glycogen storage disease type Ⅱ
    Subjects: “...Glycogen storage disease type Ⅱ...”
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    Article
  16. 16
    A New Mutation Causing Severe Infantile-Onset Pompe Disease Responsive to Enzyme Replacement Therapy
    Subjects: “...Glycogen storage disease type II...”
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    Article
  17. 17
    Homozygotic intronic GAA mutation in three siblings with late-onset Pompe's disease Mutação homozigótica intrônica no gene GAA em três irmãos com doença de Pompe de início tardio
    Subjects: “...glycogen storage disease type II...”
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    Article
  18. 18
    Molecular basis and clinical management of Pompe disease
    Subjects: “...Pompe disease, glycogen storage disease type II, acid a-glucosidase, acid maltase, metabolic...”
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    Article
  19. 19
    Pregnancy Outcomes in Late Onset Pompe Disease
    Subjects: “...glycogen storage disease type II...”
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    Article
  20. 20
    Public support for neonatal screening for Pompe disease, a broad-phenotype condition
    Subjects: “...Glycogen storage disease type II...”
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    Article
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