Glycogenosis type Ib complicated by severe granulocytopenia resembling inherited neutropenia (Q72017785)

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22 October 2019

title

Glycogenosis type Ib complicated by severe granulocytopenia resembling inherited neutropenia (English)

1 reference

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22 October 2019

author name string

C R Bartram

1

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22 October 2019

H Przyrembel

2

1 reference

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22 October 2019

U Wendel

3

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22 October 2019

H J Bremer

4

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22 October 2019

J Schaub

5

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22 October 2019

J R Haas

6

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22 October 2019

publication date

1 September 1981

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European Journal of Pediatrics

22 October 2019

published in

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22 October 2019

volume

137

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22 October 2019

issue

1

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22 October 2019

page(s)

81-84

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https://scigraph.springernature.com/pub.10.1007/bf00441175

22 October 2019

exact match

0 references

cites work

Differentiation between glycogenosis types Ia and Ib by measurement of extra respiration during phagocytosis by polymorphonuclear leukocytes?

1 reference

12 December 2020

Neutropenia in a patient with type IB glycogen storage disease: In vitro response to lithium chloride

1 reference

12 December 2020

Studies on a patient with in vivo evidence of type I glycogenosis and normal enzyme activities in vitro

1 reference

12 December 2020

A new variant of glycogen storage disease type 1: Probably due to a defect in the glucose‐6‐phosphate transport system

1 reference

12 December 2020

Nocturnal Gastric Drip Feeding in Glucose-6-Phosphatase Deficient Children

1 reference

12 December 2020

Human bone marrow colony growth in agar-gel

1 reference

12 December 2020

In vivo evidence for defective activity of glucose-6-phosphatase in type IB glycogenosis

1 reference

12 December 2020

Congenital Neutropenia: In Vitro Growth of Colonies Mimicking the Disease

1 reference

12 December 2020

Two cases of unusual type I glycogenosis

1 reference

12 December 2020

[Hepatic glycogenosis without known enzyme deficiency with clinical and biological signs of type I Cori disease]

1 reference

12 December 2020

STUDIES OF GLYCOGEN METABOLISM IN LIVER GLYCOGEN DISEASE (VON GIERKE'S DISEASE): SIX CASES WITH SIMILAR METABOLIC ABNORMALITIES AND RESPONSES TO GLUCAGON

1 reference

12 December 2020

[Glycogen storage disease type I with normal in vitro activity of glucose-6-phosphatase (author's transl)]

1 reference

12 December 2020

Type Ib glycogen storage disease is caused by a defect in the glucose-6-phosphate translocase of the microsomal glucose-6-phosphatase system

1 reference

12 December 2020

Functional differentiation of glycogenoses of the liver with respect to the use of glycerol.

1 reference

12 December 2020

Type I glycogen storage disease: five years of management with nocturnal intragastric feeding

1 reference

12 December 2020

Nocturnal Intragastric Infusion of Glucose in Management of Defective Gluconeogenesis With Hypoglycemia

1 reference

12 December 2020

Glycogenosis type Ib. Further evidence for a membrane disease

1 reference

12 December 2020

Studies of liver glycogenoses, with particular reference to the metabolism of intravenously administered glycerol.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Clinical aspects and enzymologic diagnosis of glycogenosis type 1

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00441175

1 reference

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22 October 2019

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