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Glycogen storage diseases. Phenotypic, genetic, and biochemical characteristics, and therapy.
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10609121
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10609121%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
review article
1 reference
stated in
Europe PubMed Central
title
Glycogen storage diseases. Phenotypic, genetic, and biochemical characteristics, and therapy
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10609121
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10609121%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
main subject
glycogen metabolic process
1 reference
based on heuristic
inferred from title
author
Ingrid A Holm
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10609121
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10609121%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
author name string
J I Wolfsdorf
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10609121
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10609121%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
D A Weinstein
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10609121
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10609121%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
publication date
1 December 1999
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10609121
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10609121%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
published in
Endocrinology and Metabolism Clinics of North America
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10609121
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10609121%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
volume
28
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10609121
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10609121%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10609121
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10609121%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
page(s)
801-823
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10609121
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10609121%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
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1 reference
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Crossref
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Crossref
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7 January 2021
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Hyperfiltration and renal disease in glycogen storage disease, type I
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Crossref
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https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
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Human glycogen debranching enzyme gene (AGL): complete structural organization and characterization of the 5' flanking region
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7 January 2021
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Oral complications in type 1B glycogen storage disease
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Crossref
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7 January 2021
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Neutropenia and impaired neutrophil migration in type IB glycogen storage disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
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Glycogen storage disease I and hepatocellular tumours
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7 January 2021
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Cornstarch therapy in a patient with type III glycogen storage disease
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Crossref
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https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
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Construction of a transcription map surrounding the BRCA1 locus of human chromosome 17
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
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Molecular pathology of glucose-6-phosphatase
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
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The molecular basis of the type 1 glycogen storage diseases
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Glucose-6-phosphatase proteins of the endoplasmic reticulum
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Diagnosis of type 1B and 1C glycogen storage disease
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Crossref
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https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
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A new microtechnique for the analysis of the human hepatic microsomal glucose-6-phosphatase system
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
DIAGNOSIS OF TYPE 1a AND TYPE 1c GLYCOGEN STORAGE DISEASES IN ADULTS
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
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Identification of the human hepatic microsomal glucose-6-phosphatase enzyme.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
The molecular basis of the hepatic microsomal glucose-6-phosphatase system
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Comparison of the effects of total parenteral nutrition, continuous intragastric feeding, and portacaval shunt on a patient with type I glycogen storage disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
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Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinase PHKA2 gene
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7 January 2021
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Mutations in the liver glycogen phosphorylase gene (PYGL) underlying glycogenosis type VI
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal glycogenosis of liver and muscle due to phosphorylase kinase deficiency is caused by mutations in the phosphorylase kinase beta subunit (PHKB).
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
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inferred from DOI database lookup
Liver glycogenosis due to phosphorylase kinase deficiency: PHKG2 gene structure and mutations associated with cirrhosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Renal disease in type I glycogen storage disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Cornstarch therapy in type I glycogen-storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Amelioration of proximal renal tubular dysfunction in type I glycogen storage disease with dietary therapy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation analysis in 24 French patients with glycogen storage disease type 1a.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Glycogen debranching enzyme deficiency: Long‐term study of serum enzyme activities and clinical features
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Glycogen storage disease type III (glycogen debranching enzyme deficiency): correlation of biochemical defects with myopathy and cardiomyopathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Type la glycogenosis associated with hepatocellular carcinoma
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Use of platelets, mononuclear and polymorphonuclear cells in the diagnosis of glycogen storage disease type VI
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
cDNA cloning of a liver isoform of the phosphorylase kinase alpha subunit and mapping of the gene to Xp22.2-p22.1, the region of human X-linked liver glycogenosis
1 reference
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Crossref
reference URL
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7 January 2021
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Debrancher deficiency: Neuromuscular disorder in 5 adults
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Immunoblot analyses of glycogen debranching enzyme in different subtypes of glycogen storage disease type III
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Value of the glucagon test in screening for hepatic glycogen storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Localisation of the gene for glycogen storage disease type 1c by homozygosity mapping to 11q
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ketosis in hepatic glycogenosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glucose-6-phosphatase structure, regulation, and function: an update
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Type I glycogen storage disease with vasoconstrictive pulmonary hypertension
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sequence of a putative glucose 6-phosphate translocase, mutated in glycogen storage disease type Ib
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Continuous nocturnal intragastric feeding for management of type 1 glycogen-storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Type I glycogen storage disease: five years of management with nocturnal intragastric feeding
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hyperlipidemia and fatty acid composition in patients treated for type IA glycogen storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Efficacy of cornstarch therapy in type III glycogen-storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Type IIIb glycogen storage disease associated with end-stage cirrhosis and hepatocellular carcinoma. The Liver Transplant Group
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pulmonary hypertension in type I glycogen storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of cornstarch treatment in very young children with type I glycogen storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new model for the membrane topology of glucose-6-phosphatase: the enzyme involved in von Gierke disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked liver glycogenosis: localization and isolation of a candidate gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of a new type of X-linked liver glycogenosis to the chromosomal region Xp22 containing the liver alpha-subunit of phosphorylase kinase (PHKA2)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Control of Glycogen Metabolism in the Liver
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatic Adenomata With Type 1 Glycogen Storage Disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type Ia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phosphorylase b kinase deficiency glycogenosis with cirrhosis of the liver
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new mutation of the glucose-6-phosphatase gene in a 4-year-old girl with oligosymptomatic glycogen storage disease type 1a
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chronic pancreatitis in a child with glycogen storage disease type 1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pulmonary hypertension in glycogen storage disease type I
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A case of glycogen storage disease type III (glycogen debranching enzyme deficiency) with liver cirrhosis and hypertrophic cardiomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular analysis of glycogen storage disease type Ib: identification of a prevalent mutation among Japanese patients and assignment of a putative glucose-6-phosphate translocase gene to chromosome 11
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatocellular adenomas in glycogen storage disease type I and III: a series of 43 patients and review of the literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen-storage disease. A study of phosphorylase kinase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The hepatic glycogen storage diseases--problems beyond childhood
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hyperlipidaemia does not impair vascular endothelial function in glycogen storage disease type 1a
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glomerular and tubular function in glycogen storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparison of the functional significance of left ventricular hypertrophy in hypertrophic cardiomyopathy and glycogenosis type III
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic analysis of the glucose-6-phosphatase mutation of type 1a glycogen storage disease in a Chinese family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glucose-6-phosphatase dependent substrate transport in the glycogen storage disease type-1a mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of mutations in the gene for glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1a
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the glucose-6-phosphatase gene are associated with glycogen storage disease types 1a and 1aSP but not 1b and 1c
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Infantile Hypoglycaemia due to Inherited Deficiency of Glycogen Synthetase in Liver
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatocellular carcinoma in type I glycogen storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phosphorylase b kinase deficiency in a boy with glycogenosis affecting both liver and muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the testis/liver isoform of the phosphorylase kinase gamma subunit (PHKG2) cause autosomal liver glycogenosis in the gsd rat and in humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biochemical diagnosis of hepatic glycogen storage diseases: 20 years French experience
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure and mutation analysis of the glycogen storage disease type 1b gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A man with type III glycogenosis associated with cirrhosis and portal hypertension
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Verification of diagnosis in a 17-year-old boy with clinical glycogen storage disease type Ia by mutation screening
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Proximal renal tubular acidosis in a child with type 1 glycogen storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hemorrhagic pancreatitis in a patient with glycogen storage disease type I
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gross cardiac involvement in glycogen storage disease type 3
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Radiography of glycogen storage diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Case report: hepatic adenoma with bone marrow metaplasia in a patient with glycogen storage disease type 1a
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiac involvement in glycogen storage disease type III
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Proximal renal tubular acidosis associated with glycogen storage disease, type 9
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Uncooked cornstarch treatment for hepatic phosphorylase kinase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new variant of glycogen storage disease Type I probably due to a defect in the glucose-6-phosphate transport system
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glycogen storage disease type 1b: genetic disorder involving the transport system of intracellular membrane.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of human hepatic microsomal glucose-6-phosphatase in clinical conditions where the T2 pyrophosphate/phosphate transport protein is absent
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Human Liver Glycogen Synthase Isozyme Gene Is Located on the Short Arm of Chromosome 12
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive pulmonary hypertension: a fatal complication of type I glycogen storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a point mutation (G727T) in the glucose-6-phosphatase gene in Japanese patients with glycogen storage disease type 1a, and carrier screening in healthy volunteers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiac involvement in glycogen storage disease III: morphologic and biochemical characterization with endomyocardial biopsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the liver glycogen synthase gene in children with hypoglycemia due to glycogen storage disease type 0
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transmembrane topology of glucose-6-phosphatase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glycogen storage disease type 1a in Israel: biochemical, clinical, and mutational studies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of the mutations in the glucose-6-phosphatase gene in Israeli patients with glycogen storage disease type 1a: R83C in six Jews and a novel V166G mutation in a Muslim Arab
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatic adenoma: MR characteristics and correlation with pathologic findings
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Roentgenographic skeletal changes in the glycogen storage diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Renal function and kidney size in glycogen storage disease type I.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Renal complications in glycogen storage disease type I
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nephrolithiasis, hypocitraturia, and a distal renal tubular acidification defect in type 1 glycogen storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Brief report: treatment of chronic inflammatory bowel disease in glycogen storage disease type Ib with colony-stimulating factors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inflammatory bowel disease in glycogen storage disease type Ib
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Management of hepatic adenoma in glycogen storage disease Ia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oral manifestations in glycogen storage disease type 1b
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chronic inflammatory bowel disease in glycogen storage disease type 1B
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glycogen storage disease type Ib.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glucose-6-phosphate: a key compound in glycogenosis I and favism leading to hyper- or hypolipidaemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Odd forms of inflammatory bowel disease: What can they tell us?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in exon 3 of the glycogen debranching enzyme gene are associated with glycogen storage disease type III that is differentially expressed in liver and muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Amino acid disturbances in type III glycogenosis: Differences from type I glycogenosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reversal of debrancher deficiency myopathy by the use of high-protein nutrition.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The long-term outcome of patients with glycogen storage disease type Ia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The dietary treatment of children with type I glycogen storage disease with slow release carbohydrate.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pathologic studies of the osteoporosis of Von Gierke's disease (glycogenosis 1a)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glycogen storage disease type III associated with ventricular tachycardia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glycogen storage disease in adults
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Subgroups of Type III Glycogenosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A gene on chromosome 11q23 coding for a putative glucose- 6-phosphate translocase is mutated in glycogen-storage disease types Ib and Ic.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A direct method for the diagnosis of human hepatic type 1b and type 1c glycogen-storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transverse topology of glucose-6-phosphatase in rat hepatic endoplasmic reticulum
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The identification of T2; the phosphate/pyrophosphate transport protein of the hepatic microsomal glucose-6-phosphatase system
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification and characterization of a hepatic microsomal glucose transport protein. T3 of the glucose-6-phosphatase system?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning and expression of a hepatic microsomal glucose transport protein. Comparison with liver plasma-membrane glucose-transport protein GLUT 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Regional mapping of a liver alpha-subunit gene of phosphorylase kinase (PHKA) to the distal region of human chromosome Xp
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inflammatory bowel disease in glycogen storage disease type Ib
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The natural history of liver glycogenosis due to phosphorylase kinase deficiency: a longitudinal study of 41 patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biochemical evidence for the requirement of continuous glucose therapy in young adults with type 1 glycogen storage disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Optimal daytime feeding regimen to prevent postprandial hypoglycemia in type 1 glycogen storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glucose therapy for glycogenosis type 1 in infants: comparison of intermittent uncooked cornstarch and continuous overnight glucose feedings
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Metabolic control and renal dysfunction in type I glycogen storage disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Continuous glucose for treatment of patients with type 1 glycogen-storage disease: comparison of the effects of dextrose and uncooked cornstarch on biochemical variables
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of the human glycogen debrancher gene to chromosome 1p21.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Renal lesion of type Ia glycogen storage disease: the glomerular size and renal localization of apolipoprotein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatorenal glycogenosis (type I glycogenosis) and carcinoma of the liver.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0889-8529%2805%2970103-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0889-8529(05)70103-1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10609121
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10609121%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
PubMed publication ID
10609121
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10609121
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10609121%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
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