(Q79707389)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17270480%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

title

Rapid diagnosis of late-onset Pompe disease by fluorometric assay of alpha-glucosidase activities in dried blood spots (English)

1 reference

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25 December 2019

3

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25 December 2019

author name string

Helmut Kallwass

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17270480%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Cortney Carr

2

1 reference

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25 December 2019

Mariah Titlow

4

1 reference

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25 December 2019

Robert Pomponio

5

1 reference

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25 December 2019

Deeksha Bali

6

1 reference

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25 December 2019

Jian Dai

7

1 reference

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25 December 2019

Priya Kishnani

8

1 reference

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25 December 2019

Alison Skrinar

9

1 reference

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25 December 2019

Deyanira Corzo

10

1 reference

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25 December 2019

Joan Keutzer

11

1 reference

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25 December 2019

publication date

31 January 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17270480%20AND%20SRC:MED&resulttype=core&format=json

Molecular Genetics and Metabolism

25 December 2019

published in

1 reference

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25 December 2019

volume

90

1 reference

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25 December 2019

issue

4

1 reference

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25 December 2019

page(s)

449-452

1 reference

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

25 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

The natural course of non-classic Pompe's disease; a review of 225 published cases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: results of a phase I/II clinical trial

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

Chinese hamster ovary cell-derived recombinant human acid alpha-glucosidase in infantile-onset Pompe disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

Safety and efficacy of recombinant acid alpha-glucosidase (rhGAA) in patients with classical infantile Pompe disease: results of a phase II clinical trial.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

Acid alpha-glucosidase deficiency (glycogenosis type II, Pompe disease).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

Alpha glucosidases in white blood cells, with reference to the detection of acid α 1–4 glucosidase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

Lysosomal storage of glycogen as a sequel of alpha-glucosidase inhibition by the absorbed deoxynojirimycin derivative emiglitate (BAYo1248). A drug-induced pattern of hepatic glycogen storage mimicking Pompe's disease (glycogenosis type II)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

Lysosomal glycogen accumulation in rat liver and its in vivo kinetics after a single intraperitoneal injection of acarbose, an alpha-glucosidase inhibitor

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

Lysosomal glycogen storage induced by Acarbose, a 1,4-alpha-glucosidase inhibitor

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

A new diagnostic assay for glycogen storage disease type II in mixed leukocytes.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

Comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid alpha-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2006.12.006

10.1016/J.YMGME.2006.12.006

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17270480%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

1 reference