A new variant of type IV glycogenosis: Deficiency of branching enzyme activity without apparent progressive liver disease-Reference-Cited by-同舟云学术

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A new variant of type IV glycogenosis: Deficiency of branching enzyme activity without apparent progressive liver disease

Published:1988-03 Issue:2 Volume:8 Page:302-306
ISSN:0270-9139
Container-title:Hepatology
language:en
Short-container-title:Hepatology

Author:

Greene Harry L.,Brown Barbara I.,McClenathan Daniel T.,Agostini Rocco M.,Taylor Suzanne R.

Publisher

Wiley

Subject

Hepatology

Reference18 articles.

1. Lack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis.

2. Diagnosis of glycogen storage disease. In: ed. Congenital metabolic diseases: diagnosis and treatment. New York: Marcel Dekker, Inc., 1985: 227–250.

3. Type IV Glycogen-storage Disease: Light-microscopic, Electron-microscopic, and Enzymatic Study

4. A juvenile variant of glycogenosis IV (Andersen disease)

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1. Glycogen storage diseases: An update;World Journal of Gastroenterology;2023-07-07

2. Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource;Molecular Genetics and Metabolism;2023-03

3. A novel approach to characterize phenotypic variation in GSD IV: Reconceptualizing the clinical continuum;Frontiers in Genetics;2022-09-13

4. Prenatal Diagnosis of Disorders of Carbohydrate Metabolism;Genetic Disorders and the Fetus;2021-04-20

5. Liver Transplantation for Glycogen Storage Disease Type IV;Frontiers in Pediatrics;2021-02-19

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