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Items: 1 to 20 of 21

1.

Clinical and laboratory findings in four patients with the non-progressive hepatic form of type IV glycogen storage disease.

McConkie-Rosell A, Wilson C, Piccoli DA, Boyle J, DeClue T, Kishnani P, Shen JJ, Boney A, Brown B, Chen YT.

J Inherit Metab Dis. 1996;19(1):51-8.

PMID:
8830177
2.
3.

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.

4.

Glycogen Storage Disease Type IV.

Magoulas PL, El-Hattab AW.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2013 Jan 3.

5.

Nutrition therapy for hepatic glycogen storage diseases.

Goldberg T, Slonim AE.

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

PMID:
8245377
6.

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
7.

Glycogen storage disease type III-hepatocellular carcinoma a long-term complication?

Demo E, Frush D, Gottfried M, Koepke J, Boney A, Bali D, Chen YT, Kishnani PS.

J Hepatol. 2007 Mar;46(3):492-8. Epub 2006 Nov 9. Review.

8.

[Severe cardiomyopathy revealing amylopectinosis. Two cases in adolescents from the same family].

de La Blanchardière A, Vayssier C, Duboc D, Jacquemin IE, Eymard B, Fardeau M, Maire I, Dreyfus G, Guérin F.

Presse Med. 1994 Jun 25;23(24):1124-7. Review. French.

PMID:
7971833
9.

Glycogen storage diseases.

Hug G.

Birth Defects Orig Artic Ser. 1976;12(6):145-75. Review.

PMID:
788807
10.

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
11.

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

Shin YS.

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

PMID:
17027861
12.

Pompe disease (glycogen storage disease type II): clinical features and enzyme replacement therapy.

van der Beek NA, Hagemans ML, van der Ploeg AT, Reuser AJ, van Doorn PA.

Acta Neurol Belg. 2006 Jun;106(2):82-6. Review.

PMID:
16898258
13.

Glycogen storage disease type III with muscle involvement: reappraisal of phenotypic variability and prognosis.

Momoi T, Sano H, Yamanaka C, Sasaki H, Mikawa H.

Am J Med Genet. 1992 Mar 1;42(5):696-9. Review.

PMID:
1632441
14.

Molecular characterization of glycogen storage disease type III.

Shen JJ, Chen YT.

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

PMID:
11949933
15.

Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex.

Chou JY, Matern D, Mansfield BC, Chen YT.

Curr Mol Med. 2002 Mar;2(2):121-43. Review.

PMID:
11949931
16.

[Differential diagnosis of glycogenoses].

Rozenfel'd EL, Popova IA.

Arkh Patol. 1980;42(12):61-71. Review. Russian.

PMID:
7011274
17.

Glycogen storage diseases: new perspectives.

Ozen H.

World J Gastroenterol. 2007 May 14;13(18):2541-53. Review.

18.

Liver transplantation in children with glycogen storage disease: controversies and evaluation of the risk/benefit of this procedure.

Davis MK, Weinstein DA.

Pediatr Transplant. 2008 Mar;12(2):137-45. doi: 10.1111/j.1399-3046.2007.00803.x. Review.

PMID:
18307661
19.

The hepatic glycogen storage diseases--problems beyond childhood.

Lee PJ, Leonard JV.

J Inherit Metab Dis. 1995;18(4):462-72. Review.

PMID:
7494404
20.

Investigation and management of the hepatic glycogen storage diseases.

Bhattacharya K.

Transl Pediatr. 2015 Jul;4(3):240-8. doi: 10.3978/j.issn.2224-4336.2015.04.07. Review.

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