Glycogen storage disease type Ia in canines: a model for human metabolic and genetic liver disease (Q34521347)

2 August 2017

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Glycogen storage disease type Ia in canines: a model for human metabolic and genetic liver disease (English)

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glycogen storage disease I

2 August 2017

main subject

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biomedical investigative technique

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19 September 2019

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1 October 2020

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3 December 2020

glycogen metabolic process

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inferred from title

author

Martha Campbell-Thompson

object named as

Martha Campbell-Thompson

6

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author name string

Andrew Specht

1

1 reference

2 August 2017

Laurie Fiske

2

1 reference

2 August 2017

Kirsten Erger

3

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2 August 2017

Travis Cossette

4

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2 August 2017

John Verstegen

5

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2 August 2017

Maggie B Struck

7

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2 August 2017

Young Mok Lee

8

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2 August 2017

Janice Y Chou

9

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2 August 2017

Barry J Byrne

10

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2 August 2017

Catherine E Correia

11

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2 August 2017

Cathryn S Mah

12

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2 August 2017

David A Weinstein

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2 August 2017

Thomas J Conlon

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2 August 2017

publication date

3 January 2011

10 references

Journal of Biomedicine and Biotechnology

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2011

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2 August 2017

page(s)

646257

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Creative Commons Attribution 3.0 Unported

2 August 2017

copyright license

start time

1 January 2011

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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April 2022 Public Data File from Crossref

copyrighted

0 references

cites work

Complete normalization of hepatic G6PC deficiency in murine glycogen storage disease type Ia using gene therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Adeno-associated virus-mediated correction of a canine model of glycogen storage disease type Ia.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Use of modified cornstarch therapy to extend fasting in glycogen storage disease types Ia and Ib.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Necrotic foci, elevated chemokines and infiltrating neutrophils in the liver of glycogen storage disease type Ia.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Neutrophilia and elevated serum cytokines are implicated in glycogen storage disease type Ia.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Glycogen storage diseases: new perspectives

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Gene therapy for type I glycogen storage diseases

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Glycogen storage disease types I and II: treatment updates

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Glycogen storage diseases

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Effect of continuous glucose therapy with uncooked cornstarch on the long-term clinical course of type 1a glycogen storage disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I).

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Canine model and genomic structural organization of glycogen storage disease type Ia (GSD Ia).

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Glycogen storage disease type Ia: recent experience with mutation analysis, a summary of mutations reported in the literature and a newly developed diagnostic flow chart

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Gene repair using chimeric RNA/DNA oligonucleotides

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Glucose-6-phosphatase dependent substrate transport in the glycogen storage disease type-1a mouse

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Identification of mutations in the gene for glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1a

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Mutations in the glucose-6-phosphatase gene are associated with glycogen storage disease types 1a and 1aSP but not 1b and 1c

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Genetic basis of glycogen storage disease type 1a: prevalent mutations at the glucose-6-phosphatase locus

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

The dietary treatment of children with type I glycogen storage disease with slow release carbohydrate.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Growth in glycogen-storage disease type 1. Evaluation of endocrine function.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Glycogen storage disease: recommendations for treatment

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Physical growth and development of children with type 1 glycogen-storage disease: comparison of the effects of long-term use of dextrose and uncooked cornstarch.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

Continuous glucose for treatment of patients with type 1 glycogen-storage disease: comparison of the effects of dextrose and uncooked cornstarch on biochemical variables

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

The long-term outcome of patients with glycogen storage diseases

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3027000

A novel starch for the treatment of glycogen storage diseases.

7 July 2018

1 reference

https://api.crossref.org/works/10.1155%2F2011%2F646257

The regulation of growth in glycogen storage disease type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2011%2F646257

Exercise capacity and biochemical profile during exercise in patients with glycogen storage disease type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2011%2F646257

Glycogen storage disease type Ia in two littermate Maltese puppies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2011%2F646257

Isolation and nucleotide sequence of canine glucose-6-phosphatase mRNA: identification of mutation in puppies with glycogen storage disease type Ia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2011%2F646257

Delivery of glucose-6-phosphatase in a canine model for glycogen storage disease, type Ia, with adeno-associated virus (AAV) vectors

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2011%2F646257

AAV vector-mediated reversal of hypoglycemia in canine and murine glycogen storage disease type Ia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2011%2F646257

Sustained hepatic and renal glucose-6-phosphatase expression corrects glycogen storage disease type Ia in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2011%2F646257

Continuous nocturnal intragastric feeding for management of type 1 glycogen-storage disease

21 January 2018

1 reference

12 December 2020

Cornstarch therapy in type I glycogen-storage disease

1 reference

12 December 2020

Complex carbohydrates in the dietary management of patients with glycogenosis caused by glucose-6-phosphatase deficiency

1 reference

12 December 2020

Optimal daytime feeding regimen to prevent postprandial hypoglycemia in type 1 glycogen storage disease

1 reference

12 December 2020

Identifiers

DOI

10.1155/2011/646257

1 reference

2 August 2017

1 reference

2 August 2017

1 reference