Hepatic Manifestations in Glycogen Storage Disease Type III-Reference-Cited by-同舟云学术

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Hepatic Manifestations in Glycogen Storage Disease Type III

Published:2018-11-05 Issue:4 Volume:6 Page:233-240
ISSN:2167-485X
Container-title:Current Pathobiology Reports
language:en
Short-container-title:Curr Pathobiol Rep

Author:

Korlimarla Aditi,Austin Stephanie,Sun Baodong,Kishnani Priya

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Cell Biology,Molecular Biology,Pathology and Forensic Medicine

Link

http://link.springer.com/article/10.1007/s40139-018-0182-x/fulltext.html

Reference50 articles.

1. Illingworth B, Cori GT, Cori CF. Amylo-1, 6-glucosidase in muscle tissue in generalized glycogen storage disease. J Biol Chem. 1956;218(1):123–9.

2. Bao Y, Dawson JTL, Chen Y-T. Human glycogen debranching enzyme gene (AGL): complete structural organization and characterization of the 5′ flanking region. Genomics. 1996;38(2):155–65.

3. Ding J-H, de Barsy T, Brown BI, Coleman RA, Chen YT. Immunoblot analyses of glycogen debranching enzyme in different subtypes of glycogen storage disease type III. J Pediatr. 1990;116(1):95–100.

4. Coleman RA, Winter HS, Wolf B, Chen YT. Glycogen debranching enzyme deficiency: long-term study of serum enzyme activities and clinical features. J Inherit Metab Dis. 1992;15(6):869–81.

5. Talente GM, Coleman RA, Alter C, Baker L, Brown BI, Cannon RA, et al. Glycogen storage disease in adults. Ann Intern Med. 1994;120(3):218–26.

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1. Glycogen Storage Diseases;Nutrition Management of Inherited Metabolic Diseases;2022

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