Lysosomal dysfunction in muscle with special reference to glycogen storage disease type II. (Q35084348)

6 August 2017

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title

Lysosomal dysfunction in muscle with special reference to glycogen storage disease type II. (English)

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ORCID Public Data File 2021

6 August 2017

glycogen storage disease

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author name string

Reinout P Hesselink

1

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6 August 2017

Anton J M Wagenmakers

2

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6 August 2017

Maarten R Drost

3

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6 August 2017

Ger J Van der Vusse

4

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6 August 2017

language of work or name

English

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publication date

1 March 2003

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6 August 2017

7

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Biochimica et Biophysica Acta

inferred from page(s)

published in

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6 August 2017

1637

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6 August 2017

164-170

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6 August 2017

2

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Lysosomal storage diseases

6 August 2017

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Lysosomal Storage Diseases

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Cellular pathology of lysosomal storage disorders.

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alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease).

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Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling

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Autocatalytic inactivation of lysosomal cathepsins is associated with inhibition of protein breakdown by insulin-like growth factor-1 (IGF-1) in myotubes

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Identifiers

DOI

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6 August 2017

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