23070616 21491105 20699197 32428104 34627694 29972110 23412857 21620087 25633903 21599942 28914857 24011870 23738826 - Search Results

Year	Number of Results
2010	1
2011	3
2012	1
2013	4
2015	1
2017	1
2018	1
2020	1
2021	1
2022	0

1

iPS cell modeling of cardiometabolic diseases.

Nakamura K, Hirano K, Wu SM. Nakamura K, et al. J Cardiovasc Transl Res. 2013 Feb;6(1):46-53. doi: 10.1007/s12265-012-9413-4. Epub 2012 Oct 16. J Cardiovasc Transl Res. 2013. PMID: 23070616 Free PMC article. Review.

2

Dietary dilemmas in the management of glycogen storage disease type I.

Bhattacharya K. Bhattacharya K. J Inherit Metab Dis. 2011 Jun;34(3):621-9. doi: 10.1007/s10545-011-9322-8. Epub 2011 Apr 14. J Inherit Metab Dis. 2011. PMID: 21491105 Review.

3

Ischemic stroke in an adult with glycogen storage disease type I.

Goulart JM, Yoo JY, Kirchoff-Torres KF, Delman BN, Tuhrim S. Goulart JM, et al. J Clin Neurosci. 2010 Nov;17(11):1467-9. doi: 10.1016/j.jocn.2010.03.026. Epub 2010 Aug 10. J Clin Neurosci. 2010. PMID: 20699197

4

Glycogen Storage Disease Type I (Von Gierke disease): Report of Two Cases with Severe Dyslipidemia.

Ballavenuto JMA, Oliveira JDÓD, Alves RJ. Ballavenuto JMA, et al. Arq Bras Cardiol. 2020 Apr;114(4 Suppl 1):23-26. doi: 10.36660/abc.20190037. Epub 2020 May 18. Arq Bras Cardiol. 2020. PMID: 32428104 Free PMC article. English, Portuguese. No abstract available.

5

Glycogen storage disease type I patients with hyperlipidemia have no signs of early vascular dysfunction and premature atherosclerosis.

Schmitt J, Wurm M, Schwab KO, Spiekerkoetter U, Hannibal L, Grünert SC. Schmitt J, et al. Nutr Metab Cardiovasc Dis. 2021 Nov 29;31(12):3384-3392. doi: 10.1016/j.numecd.2021.08.027. Epub 2021 Aug 13. Nutr Metab Cardiovasc Dis. 2021. PMID: 34627694

6

De novo aortopathy and cardiovascular outcomes in paediatric liver transplant recipients.

Huang JG, Lim T, Quek SC, Quak SH, Aw MM. Huang JG, et al. Cardiol Young. 2018 Aug;28(8):986-994. doi: 10.1017/S104795111800063X. Epub 2018 Jul 4. Cardiol Young. 2018. PMID: 29972110

7

Asymmetric dimethylarginine (ADMA) and L-arginine levels in children with glycogen storage disease type I.

Kasapkara ÇS, Tümer L, Biberoglu G, Kasapkara A, Hasanoğlu A. Kasapkara ÇS, et al. J Pediatr Endocrinol Metab. 2013;26(5-6):427-31. doi: 10.1515/jpem-2012-0306. J Pediatr Endocrinol Metab. 2013. PMID: 23412857

8

Preemptive liver-kidney transplantation in von Gierke disease: a case report.

Marega A, Fregonese C, Tulissi P, Vallone C, Gropuzzo M, Toniutto PL, Baccarani U, Bresadola F, Toso F, Montanaro D. Marega A, et al. Transplant Proc. 2011 May;43(4):1196-7. doi: 10.1016/j.transproceed.2011.03.003. Transplant Proc. 2011. PMID: 21620087

9

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

Derks TG, van Rijn M. Derks TG, et al. J Inherit Metab Dis. 2015 May;38(3):537-43. doi: 10.1007/s10545-015-9811-2. Epub 2015 Jan 30. J Inherit Metab Dis. 2015. PMID: 25633903 Free PMC article. Review.

10

Glucose-6-phosphatase deficiency.

Froissart R, Piraud M, Boudjemline AM, Vianey-Saban C, Petit F, Hubert-Buron A, Eberschweiler PT, Gajdos V, Labrune P. Froissart R, et al. Orphanet J Rare Dis. 2011 May 20;6:27. doi: 10.1186/1750-1172-6-27. Orphanet J Rare Dis. 2011. PMID: 21599942 Free PMC article. Review.

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