(Q84395634)

English

Urine analysis of glucose tetrasaccharide by HPLC; a useful marker for the investigation of patients with Pompe and other glycogen storage diseases

scientific article published on 18 June 2011

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21687968%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

Urine analysis of glucose tetrasaccharide by HPLC; a useful marker for the investigation of patients with Pompe and other glycogen storage diseases (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21687968%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

author name string

Victoria Manwaring

1

1 reference

Europe PubMed Central

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5 February 2020

Helen Prunty

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21687968%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

Katie Bainbridge

3

1 reference

Europe PubMed Central

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5 February 2020

Derek Burke

4

1 reference

Europe PubMed Central

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5 February 2020

Niamh Finnegan

5

1 reference

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5 February 2020

Rebecca Franses

6

1 reference

Europe PubMed Central

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5 February 2020

Amanda Lam

7

1 reference

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5 February 2020

Ashok Vellodi

8

1 reference

Europe PubMed Central

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5 February 2020

Simon Heales

9

1 reference

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5 February 2020

publication date

18 June 2011

1 reference

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5 February 2020

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

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5 February 2020

35

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5 February 2020

2

1 reference

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5 February 2020

311-316

1 reference

Europe PubMed Central

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5 February 2020

https://scigraph.springernature.com/pub.10.1007/s10545-011-9360-2

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Therapeutic approaches in glycogen storage disease type II/Pompe Disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The identity and origin of oligosaccharides present in the faeces and urine of sick infants

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucose tetrasaccharide as a biomarker for monitoring the therapeutic response to enzyme replacement therapy for Pompe disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzyme analysis for Pompe disease in leukocytes; superior results with natural substrate compared with artificial substrates.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term intravenous treatment of Pompe disease with recombinant human alpha-glucosidase from milk

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitation of a urinary tetrasaccharide by gas chromatography and mass spectrometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methods for a prompt and reliable laboratory diagnosis of Pompe disease: report from an international consensus meeting

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term monitoring of patients with infantile-onset Pompe disease on enzyme replacement therapy using a urinary glucose tetrasaccharide biomarker.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of a glucose tetrasaccharide elevated in Pompe disease by stable isotope dilution–electrospray ionization tandem mass spectrometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electrochemical determination of carbohydrates: enzyme electrodes and amperometric detection in liquid chromatography and capillary electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Liquid chromatographic assay for a glucose tetrasaccharide, a putative biomarker for the diagnosis of Pompe disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21687968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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