Severe hypoglycemia as a presenting symptom of carbohydrate-deficient glycoprotein syndrome (Q73243917)

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2 November 2019

title

Severe hypoglycemia as a presenting symptom of carbohydrate-deficient glycoprotein syndrome (English)

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2 November 2019

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D Babovic-Vuksanovic

1

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2 November 2019

M C Patterson

2

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2 November 2019

W F Schwenk

3

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2 November 2019

J F O'Brien

4

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2 November 2019

J Vockley

5

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2 November 2019

H H Freeze

6

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2 November 2019

D P Mehta

7

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2 November 2019

V V Michels

8

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2 November 2019

language of work or name

English

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publication date

1 December 1999

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The Journal of Pediatrics

2 November 2019

published in

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2 November 2019

volume

135

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2 November 2019

page(s)

775-781

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2 November 2019

issue

6

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The carbohydrate-deficient glycoprotein syndromes: an overview

2 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970103-4

Carbohydrate deficient glycoprotein (CDG) syndrome type I

7 January 2021

1 reference

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The carbohydrate-deficient glycoprotein syndrome: an experiment of nature in glycosylation

7 January 2021

1 reference

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Carbohydrate-deficient glycoprotein syndrome type V: deficiency of dolichyl-P-Glc:Man9GlcNAc2-PP-dolichyl glucosyltransferase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970103-4

Disorders in protein glycosylation and potential therapy: tip of an iceberg?

7 January 2021

1 reference

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Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970103-4

Phosphomannose isomerase deficiency: a carbohydrate-deficient glycoprotein syndrome with hepatic-intestinal presentation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970103-4

Carbohydrate deficient serum transferrin in a new systemic hereditary syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970103-4

Phosphomannomutase deficiency is a cause of carbohydrate-deficient glycoprotein syndrome type I

7 January 2021

1 reference

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Inhibition of phosphomannose isomerase by fructose 1-phosphate: an explanation for defective N-glycosylation in hereditary fructose intolerance

7 January 2021

1 reference

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Hypertrophic obstructive cardiomyopathy in a neonate with the carbohydrate‐deficient glycoprotein syndrome

7 January 2021

1 reference

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A case of the carbohydrate-deficient glycoprotein syndrome type 1 (CDGS type 1) with normal phosphomannomutase activity

7 January 2021

1 reference

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Hyperinsulinemic hypoglycemia as a presenting sign in phosphomannose isomerase deficiency: A new manifestation of carbohydrate-deficient glycoprotein syndrome treatable with mannose

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970103-4

A novel disorder of N-glycosylation due to phosphomannose isomerase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970103-4

Mannose enters mammalian cells using a specific transporter that is insensitive to glucose

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970103-4

Human fibroblasts prefer mannose over glucose as a source of mannose for N-glycosylation. Evidence for the functional importance of transported mannose

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970103-4

Oral ingestion of mannose elevates blood mannose levels: a first step toward a potential therapy for carbohydrate-deficient glycoprotein syndrome type I.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970103-4

10.1016/S0022-3476(99)70103-4

7 January 2021

Identifiers

DOI

1 reference

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2 November 2019

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