Glycogen Storage Disease Type III with Hypoketosis-Reference-Cited by-同舟云学术

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Glycogen Storage Disease Type III with Hypoketosis

Published:2010-01 Issue:8 Volume:23 Page:
ISSN:0334-018X
Container-title:Journal of Pediatric Endocrinology and Metabolism
language:
Short-container-title:

Author:

Clemente María,Gussinyer Miquel,Arranz José Antonio,Riudor Encarnació,Yeste Diego,Albisu Marian,Carrascosa Antonio

Publisher

Walter de Gruyter GmbH

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Link

https://www.degruyter.com/document/doi/10.1515/jpem.2010.134/pdf

Reference6 articles.

1. Disturbed lipid metabolism in glycogen storage disease type 1

2. Clinical and genetic variability of glycogen storage disease type IIIa: Seven novelAGL gene mutations in the mediterranean area

3. Glycogen storage diseases: New perspectives

4. Glycogen Storage Disease Type III (Glycogen Debranching Enzyme Deficiency): Correlation of Biochemical Defects with Myopathy and Cardiomyopathy

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Metabolic Cardiomyopathies and Cardiac Defects in Inherited Disorders of Carbohydrate Metabolism: A Systematic Review;International Journal of Molecular Sciences;2023-05-11

2. Normoglycemic Ketonemia as Biochemical Presentation in Ketotic Glycogen Storage Disease;JIMD Reports;2015

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