(Q34954560)

5 August 2017

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title

Historical highlights and unsolved problems in glycogen storage disease type 1. (English)

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5 August 2017

main subject

glycogen storage disease

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Shimon W Moses

1

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5 August 2017

language of work or name

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23 August 2002

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European Journal of Pediatrics

5 August 2017

published in

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5 August 2017

volume

161 Suppl 1

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5 August 2017

page(s)

S2-9

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https://scigraph.springernature.com/pub.10.1007/bf02679988

5 August 2017

exact match

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cites work

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

1 reference

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Deficient glucose phosphorylation as a possible common denominator and its relation to abnormal leucocyte function, in glycogen storage disease 1b patients.

21 January 2018

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Glycogen storage disease I and hepatocellular tumours

21 January 2018

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21 January 2018

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The molecular basis of the hepatic microsomal glucose-6-phosphatase system

21 January 2018

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Cloning and expression of a hepatic microsomal glucose transport protein. Comparison with liver plasma-membrane glucose-transport protein GLUT 2

21 January 2018

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

21 January 2018

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

21 January 2018

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Renal tranplantation in type 1 glycogenosis. Failure to improve glucose metabolism

21 January 2018

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

21 January 2018

1 reference

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Defective neutrophil and monocyte functions in glycogen storage disease type Ib: a literature review

21 January 2018

1 reference

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Normal hepatic glucose production in the absence of GLUT2 reveals an alternative pathway for glucose release from hepatocytes

21 January 2018

1 reference

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Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1b.

21 January 2018

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Hepatic Adenomata With Type 1 Glycogen Storage Disease

21 January 2018

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Studies on dietary correction of metabolic abnormalities in hepatorenal glycogenosis

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF02679988

Impaired metabolic function and signaling defects in phagocytic cells in glycogen storage disease type 1b

21 January 2018

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

21 January 2018

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A new variant of glycogen storage disease Type I probably due to a defect in the glucose-6-phosphate transport system

21 January 2018

1 reference

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Analysis of human hepatic microsomal glucose-6-phosphatase in clinical conditions where the T2 pyrophosphate/phosphate transport protein is absent

21 January 2018

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Transmembrane topology of glucose-6-phosphatase

21 January 2018

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Endogenous glucose production in Type I glycogen storage disease.

21 January 2018

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Brief report: treatment of chronic inflammatory bowel disease in glycogen storage disease type Ib with colony-stimulating factors

21 January 2018

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Liver transplantation for type I and type IV glycogen storage disease

21 January 2018

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21 January 2018

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Bisphosphonates: from grandparents to grandchildren

21 January 2018

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Glycogen storage disease in adults

21 January 2018

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

21 January 2018

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Correction of glycogen storage disease type 1a in a mouse model by gene therapy

21 January 2018

1 reference

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21 January 2018

Identifiers

DOI

10.1007/BF02679988

1 reference

Dimensions Publication ID

5 August 2017

1009299119

0 references

1 reference