Focal fatty liver change in glycogenosis type 1 a-Reference-Cited by-同舟云学术

Focal fatty liver change in glycogenosis type 1 a

Published:1995-04 Issue:4 Volume:154 Page:332-332
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Lee Philip J.,Leonard James V.,Dicks-Mireaux Claire

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/BF01957374.pdf

Reference7 articles.

1. Bianchi L (1993) Glycogen storage disease I and hepatocellular tumours. Eur J Pediatr 152 [Suppl 1]:S63-S70

2. Chong VFH, Fan YF (1994) Ultrasonographic hepatic pseudolesions: normal parenchyma mimicking mass lesions in fatty liver. Clin Radiol 49:326–329

3. Conti JA, Kemeny N (1992) Type Ia glycogenosis associated with hepatocellular carcinoma. Cancer 69:1320–1322

4. Fink AS, Appelman HD, Thompson NW (1985) Hemorrhage into a hepatic adenoma and type Ia glycogen storage disease: a case report and review of the literature. Surgery 97:117–123

5. Igarashi M, Akiyama Y, Nakamura T, Ohtsuki S, Nakashima Y (1994) Focal fatty liver change in a 12-year-old Japanese boy. Eur J Pediatr 155: 429–431

Cited by 5 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. Guidelines for management of glycogen storage disease type I—European study on glycogen storage disease type I (ESGSD I);European Journal of Pediatrics;2002-10

2. Glycogen storage disease type I: pathophysiology of liver adenomas;European Journal of Pediatrics;2002-10

3. Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European study on glycogen storage disease type I (ESGSD I);European Journal of Pediatrics;2002-10

4. Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I);European Journal of Pediatrics;2002-01-01

5. The hepatic glycogen storage diseases ? problems beyond childhood;Journal of Inherited Metabolic Disease;1995