Current status of hepatic glycogen storage disease in Japan: clinical manifestations, treatments and long-term outcomes-Reference-Cited by-同舟云学术

Current status of hepatic glycogen storage disease in Japan: clinical manifestations, treatments and long-term outcomes

Published:2013-03-14 Issue:5 Volume:58 Page:285-292
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Kido Jun,Nakamura Kimitoshi,Matsumoto Shirou,Mitsubuchi Hiroshi,Ohura Toshihiro,Shigematsu Yosuke,Yorifuji Tohru,Kasahara Mureo,Horikawa Reiko,Endo Fumio

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/jhg201317.pdf

Reference49 articles.

1. Chen, Y. T., Coleman, R. A., Scheinman, J. I., Kolbeck, P. C. & Sidbury, J. B. Renal disease in type I glycogen storage disease. N. Engl. J. Med. 318, 7–11 (1988).

2. Reitsma-Bierens, W. C. Renal complications in glycogen storage disease type I. Eur. J. Pediatr. 152 (Suppl 1), S60–S62 (1993).

3. Zangeneh, F., Limbeck, G. A., Brown, B. I., Emch, J. R., Arcasoy, M. M., Goldenberg, V. E. et al. Hepatorenal glycogenosis (type I glycogenosis) and carcinoma of the liver. J. Pediatr. 74, 73–83 (1969).

4. Franco, L. M., Krishnamurthy, V., Bali, D., Weinstein, D. A., Arn, P., Clary, B. et al. Hepatocellular carcinoma in glycogen storage disease type Ia: a case series. J. Inherit. Metab. Dis. 28, 153–162 (2005).

5. Parvari, R., Moses, S., Shen, J., Hershkovitz, E., Lerner, A. & Chen, Y. T. A single-base deletion in the 3'-coding region of glycogen-debranching enzyme is prevalent in glycogen storage disease type IIIA in a population of North African Jewish patients. Eur. J. Hum. Genet. 5, 266–270 (1997).

Cited by 25 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. A case study of a liver transplant-treated patient with glycogen storage disease type Ia presenting with multiple inflammatory hepatic adenomas: an analysis of clinicopathologic and genetic data;BMC Medical Genomics;2024-05-06

2. Genotypic and phenotypic features of 39 Chinese patients with glycogen storage diseases type I, VI, and IX;Clinical Genetics;2024-04-05

3. A splice-switching oligonucleotide treatment ameliorates glycogen storage disease type 1a in mice with G6PC c.648G>T;Journal of Clinical Investigation;2023-12-01

4. Blood glucose trends in glycogen storage disease type Ia: A cross‐sectional study;Journal of Inherited Metabolic Disease;2023-06-14

5. Outcome of liver transplantation in hepatic glycogen storage disease: A systematic review and meta‐analysis;Clinical Transplantation;2022-12-07