The use of acarbose inhibition in the measurement of acid alpha-glucosidase activity in blood lymphocytes for the diagnosis of Pompe disease (Q83350404)

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scientific article published on 01 May 2006

Language	Label	Description	Also known as
English	The use of acarbose inhibition in the measurement of acid alpha-glucosidase activity in blood lymphocytes for the diagnosis of Pompe disease	scientific article published on 01 May 2006

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16702881%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

The use of acarbose inhibition in the measurement of acid alpha-glucosidase activity in blood lymphocytes for the diagnosis of Pompe disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16702881%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

author name string

Rhona M Jack

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16702881%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Cindy Gordon

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16702881%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

C R Scott

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16702881%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Priya S Kishnani

4

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16702881%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Deeksha Bali

5

1 reference

Europe PubMed Central

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21 January 2020

publication date

1 May 2006

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21 January 2020

Genetics in Medicine

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16702881%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

8

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21 January 2020

5

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21 January 2020

307-312

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21 January 2020

Pompe disease in infants and children

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

Infantile onset Pompe disease: a report of physician narratives from an epidemiologic study

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

The natural course of infantile Pompe's disease: 20 original cases compared with 133 cases from the literature

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

Carrier frequency for glycogen storage disease type II in New York and estimates of affected individuals born with the disease

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

Alpha-glucosidase activity in human leucocytes: Choice of lymphocytes for the diagnosis of Pompe's disease and the carrier state

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

White blood cells and the diagnosis of alpha-glucosidase deficiency

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

High-level production of recombinant human lysosomal acid alpha-glucosidase in Chinese hamster ovary cells which targets to heart muscle and corrects glycogen accumulation in fibroblasts from patients with Pompe disease

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

Enzyme replacement and enhancement therapies for lysosomal diseases

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

Enzyme replacement therapy in classical infantile pompe disease: results of a ten-month follow-up study

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

Recombinant human alpha-glucosidase from rabbit milk in Pompe patients.

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

Enzyme therapy for pompe disease with recombinant human alpha-glucosidase from rabbit milk

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

Anaesthetic management of infants with glycogen storage disease type II: a physiological approach

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

Glycogen storage disease type II: enzymatic screening in dried blood spots on filter paper

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

Direct multiplex assay of lysosomal enzymes in dried blood spots for newborn screening

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000217785.19262.9E

21 January 2018

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