Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I). (Q51952874)

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scientific article published on 22 August 2002

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English	Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I).	scientific article published on 22 August 2002

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scholarly article

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12373567

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

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12373567

glycogen storage disease

1 reference

based on heuristic

inferred from title

author name string

Jan Peter Rake

1

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12373567

Gepke Visser

2

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12373567

Philippe Labrune

3

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12373567

James V Leonard

4

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12373567

Kurt Ullrich

5

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12373567

G Peter A Smit

6

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12373567

publication date

22 August 2002

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Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12373567

European Journal of Pediatrics

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Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12373567

161 Suppl 1

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Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12373567

S20-34

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Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12373567

https://scigraph.springernature.com/pub.10.1007/bf02679990

0 references

The gene for glycogen-storage disease type 1b maps to chromosome 11q23.

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

On the involvement of a glucose 6-phosphate transport system in the function of microsomal glucose 6-phosphatase

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Direct evidence for the involvement of two glucose 6-phosphate-binding sites in the glucose-6-phosphatase activity of intact liver microsomes. Characterization of T1, the microsomal glucose 6-phosphate transport protein by a direct binding assay.

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Increased lipogenesis and resistance of lipoproteins to oxidative modification in two patients with glycogen storage disease type 1a.

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Glycogen storage disease I and hepatocellular tumours

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Type I glycogen storage disease: kidney involvement, pathogenesis and its treatment

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Type I glycogen storage disease: nine years of management with cornstarch

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Impaired platelet function in glucose-6-phosphatase deficiency

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Long-term outcome of liver transplantation in patients with glycogen storage disease type Ia.

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Lactate as a cerebral metabolic fuel for glucose-6-phosphatase deficient children.

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

STUDIES IN GLYCOGEN STORAGE DISEASES. I. INTESTINAL GLUCOSE-6-PHOSPHATASE ACTIVITY IN PATIENTS WITH VON GIERKE'S DISEASE AND THEIR PARENTS

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Triglyceride Clearing in Glycogen Storage Disease

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

The "muscle-bone unit" in children and adolescents: a 2000 overview

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Sequence of a putative glucose 6-phosphate translocase, mutated in glycogen storage disease type Ib

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Effects of cornstarch treatment in very young children with type I glycogen storage disease

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Defect of platelet function associated with chronic hypoglycaemia

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Effect of liver transplantation on hepatic glucose metabolism in a patient with type I glycogen storage disease.

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Hepatocellular adenomas in glycogen storage disease type I and III: a series of 43 patients and review of the literature

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

The prevalence of polycystic ovaries in the hepatic glycogen storage diseases: its association with hyperinsulinism

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Liver transplantation for glycogen storage disease types I, III, and IV

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Disordered intestinal function in glycogen storage disease

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Renal function and kidney size in glycogen storage disease type I.

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Glucose-6-phosphate: a key compound in glycogenosis I and favism leading to hyper- or hypolipidaemia

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

The long-term outcome of patients with glycogen storage diseases

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Glycogen storage disease in adults

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

The putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Decreased urinary citrate excretion in type 1a glycogen storage disease

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Plasma antioxidants in pediatric patients with glycogen storage disease, diabetes mellitus, and hypercholesterolemia.

1 reference

https://api.crossref.org/works/10.1007%2FBF02679990

21 January 2018

Identifiers

10.1007/BF02679990

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12373567

1 reference

Europe PubMed Central

18 April 2018

http://europepmc.org/abstract/MED/12373567

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