(Q39651448)

English

Glycogen storage disease: recommendations for treatment

scientific article published on April 1988

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

1 reference

Europe PubMed Central

Glycogen storage disease: recommendations for treatment (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

glycogen storage disease

1 reference

based on heuristic

inferred from title

author name string

J Fernandes

1

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

J V Leonard

2

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

S W Moses

3

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

M Odièvre

4

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

M di Rocco

5

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

J Schaub

6

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

G P Smit

7

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

K Ullrich

8

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

P Durand

9

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

publication date

1 April 1988

1 reference

Europe PubMed Central

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13 September 2017

European Journal of Pediatrics

1 reference

Europe PubMed Central

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13 September 2017

147

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13 September 2017

3

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13 September 2017

226-228

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13 September 2017

HYPOGLYCÆMIA COMPLICATING FEEDING REGIMENS FOR GLYCOGEN-STORAGE DISEASE

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperlipemia in children with liver glycogen disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hexose and protein tolerance tests in children with liver glycogenosis caused by a deficiency of the debranching enzyme system

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myopathy and growth failure in debrancher enzyme deficiency: improvement with high-protein nocturnal enteral therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regression of hepatic adenomas in type Ia glycogen storage disease with dietary therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neutropenia and impaired neutrophil function in glycogenosis type Ib

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hepatorenal glycogenosis (type I glycogenosis) and carcinoma of the liver.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haematological findings in type Ib glycogen storage disease before and after portacaval shunt

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glycogen storage disease type Ib.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intragastric feeding in type I glycogen storage disease: factors affecting the control of lactic acidemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Measurement of "true" glucose production rates in infancy and childhood with 6,6-dideuteroglucose

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Developmental changes of cerebral ketone body utilization in human infants.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effect of disaccharides on the hyperlactacidaemia of glucose-6-phosphatase-deficient children

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuromuscular involvement in glycogen storage disease type III.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cornstarch therapy in type I glycogen-storage disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urinary excretion of lactate, 2-oxoglutarate, citrate, and glycerol in patients with glycogenosis type I.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3292244

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00442683

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

release_6i5welk5lvgu3pidf6s6rdtody

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

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