Diagnosis of generalized glycogen storage disease (Pompe's disease)-Reference-Cited by-同舟云学术

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Diagnosis of generalized glycogen storage disease (Pompe's disease)

Published:1963-11 Issue:5 Volume:63 Page:984-987
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Huijing F.,van Creveld S.,Losekoot G.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference10 articles.

1. Glycogen storage disease;Humphreys;Am. J. Pathol.,1934

2. Heart disease in infancy and childhood;Keith,1958

3. Recent developments in the biochemistry of glycogen storage disease and of fructose intolerance;Hers;Chem. Weekblad,1961

4. α-Glucosidase deficiency in generalised glycogen storage disease (Pompe's disease);Hers;Biochem. J.,1963

5. Phosphorylase activity in leucocytes from patients with glycogen-storage disease;Hülsmann;Lancet,1961

Cited by 57 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. Identification of heterozygotes for glycogenosis 2 (Acid maltase deficiency);Clinical Genetics;2008-04-23

2. Sibling phenotype concordance in classical infantile Pompe disease;American Journal of Medical Genetics Part A;2007

3. Inborn Errors of Carbohydrate Metabolism;Principles of Perinatal—Neonatal Metabolism;1998

4. Skeletal Muscle and Peripheral Nerves;Fetal and Neonatal Pathology;1987

5. The “muscular variant” of Pompe disease: Clinical, biochemical and histologic characteristics;American Journal of Medical Genetics;1985-07

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