Lipids in hepatic glycogen storage diseases: pathophysiology, monitoring of dietary management and future directions

Author:

Derks Terry G. J.,van Rijn Margreet

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference43 articles.

1. Bali DS, Chen YT, Goldstein JL (1993) Glycogen storage disease type I. In: Pagon RA, Adam MP, Ardinger HH et al (eds) GeneReviews(R). University of Washington, Seattle, Seattle

2. Bandsma RH, Prinsen BH, van Der Velden MS et al (2008) Increased de novo lipogenesis and delayed conversion of large VLDL into intermediate density lipoprotein particles contribute to hyperlipidemia in glycogen storage disease type 1a. Pediatr Res 63:702–707

3. Bernier AV, Sentner CP, Correia CE, Theriaque DW, Shuster JJ, Smit GP, Weinstein DA (2008) Hyperlipidemia in glycogen storage disease type III: effect of age and metabolic control. J Inherit Metab Dis 31:729–732

4. Bernier AV, Correia CE, Haller MJ, Theriaque DW, Shuster JJ, Weinstein DA (2009) Vascular dysfunction in glycogen storage disease type I. J Pediatr 154:588–591

5. Bernstein LE, Bums CE, Wilkinson LJ, Boney A, Balliet J, Van Hove J (2010) Treatment of elevated triglycerides in glycogen storage disease type 1a and hypertriglyceridemia with medium chain triglycerides sources. J Inherit Metab Dis 33:S173–S173

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