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Items: 10

1.

Generation of a novel mouse model that recapitulates early and adult onset glycogenosis type IV.

Akman HO, Sheiko T, Tay SK, Finegold MJ, Dimauro S, Craigen WJ.

Hum Mol Genet. 2011 Nov 15;20(22):4430-9. doi: 10.1093/hmg/ddr371. Epub 2011 Aug 19.

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3.

Diffuse reticuloendothelial system involvement in type IV glycogen storage disease with a novel GBE1 mutation: a case report and review.

Magoulas PL, El-Hattab AW, Roy A, Bali DS, Finegold MJ, Craigen WJ.

Hum Pathol. 2012 Jun;43(6):943-51. doi: 10.1016/j.humpath.2011.10.001. Epub 2012 Feb 2. Review.

PMID:
22305237
4.

Neonatal presentation of lethal neuromuscular glycogen storage disease type IV.

Escobar LF, Wagner S, Tucker M, Wareham J.

J Perinatol. 2012 Oct;32(10):810-3. doi: 10.1038/jp.2011.178. Review.

PMID:
23014386
5.

[Glycogenosis type IV (branching enzyme deficiency, amylopectinosis, Andersen disease, polyglucosan body disease)].

Inui K.

Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):43-4. Review. Japanese. No abstract available.

PMID:
9589984
6.

Molecular characterization of glycogen storage disease type III.

Shen JJ, Chen YT.

Curr Mol Med. 2002 Mar;2(2):167-75. Review.

PMID:
11949933
7.

Glycogen storage disease: clinical, biochemical, and molecular heterogeneity.

Shin YS.

Semin Pediatr Neurol. 2006 Jun;13(2):115-20. Review.

PMID:
17027861
8.

Progress and problems in muscle glycogenoses.

DiMauro S, Spiegel R.

Acta Myol. 2011 Oct;30(2):96-102. Review.

9.

Liver transplantation for glycogen storage disease types I, III, and IV.

Matern D, Starzl TE, Arnaout W, Barnard J, Bynon JS, Dhawan A, Emond J, Haagsma EB, Hug G, Lachaux A, Smit GP, Chen YT.

Eur J Pediatr. 1999 Dec;158 Suppl 2:S43-8. Review.

10.

Nutrition therapy for hepatic glycogen storage diseases.

Goldberg T, Slonim AE.

J Am Diet Assoc. 1993 Dec;93(12):1423-30. Review.

PMID:
8245377

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