PubMed for id: 369842

Year	Number of Results
1992	1
1993	1
1996	1
1997	1
1998	3
1999	1
2000	3
2001	1
2002	1
2004	1
2005	1
2007	2
2008	4
2009	1
2010	1
2011	3
2012	6
2013	3
2014	4
2015	2
2016	2
2018	2
2019	2
2020	5
2021	2
2022	6
2024	0

1

Inherent lipid metabolic dysfunction in glycogen storage disease IIIa.

Li XH, Gong QM, Ling Y, Huang C, Yu DM, Gu LL, Liao XW, Zhang DH, Hu XQ, Han Y, Kong XF, Zhang XX. Li XH, et al. Biochem Biophys Res Commun. 2014 Dec 5;455(1-2):90-7. doi: 10.1016/j.bbrc.2014.10.096. Biochem Biophys Res Commun. 2014. PMID: 25451272

2

Genetic analysis and long-term treatment monitoring of 11 children with glycogen storage disease type IIIa.

Du C, Wei H, Zhang M, Hu M, Li Z, Zhang C, Luo X, Liang Y. Du C, et al. J Pediatr Endocrinol Metab. 2020 Jul 28;33(7):923-930. doi: 10.1515/jpem-2019-0453. J Pediatr Endocrinol Metab. 2020. PMID: 32623374

3

Genetic analysis and clinical assessment of four patients with Glycogen Storage Disease Type IIIa in China.

Zhang Y, Xu M, Chen X, Yan A, Zhang G, Liu Z, Qiu W. Zhang Y, et al. BMC Med Genet. 2018 Apr 4;19(1):54. doi: 10.1186/s12881-018-0560-6. BMC Med Genet. 2018. PMID: 29614965 Free PMC article.

4

[Analysis of clinical features and AGL gene mutations in a family with glycogen storage disease type IIIa].

Guo L, Lin W, Zhang Z, Zhao X, Zhang S, Cai X, Zhou Q, Song Y. Guo L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Aug;32(4):502-5. doi: 10.3760/cma.j.issn.1003-9406.2015.04.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26252094 Chinese.

5

Liver cirrhosis treated by living donor liver transplantation in a patient with AGL mutation c.2607-2610delATTC and c.1672dupA.

Kondo Y, Usui H, Ishige-Wada M, Murase T, Owada M, Okubo M. Kondo Y, et al. Clin Chim Acta. 2013 Sep 23;424:19-21. doi: 10.1016/j.cca.2013.05.007. Epub 2013 May 13. Clin Chim Acta. 2013. PMID: 23688858

6

Bulbar muscle weakness and fatty lingual infiltration in glycogen storage disorder type IIIa.

Horvath JJ, Austin SL, Jones HN, Drake EJ, Case LE, Soher BJ, Bashir MR, Kishnani PS. Horvath JJ, et al. Mol Genet Metab. 2012 Nov;107(3):496-500. doi: 10.1016/j.ymgme.2012.09.025. Epub 2012 Sep 28. Mol Genet Metab. 2012. PMID: 23062577

7

Glycogen storage disease type IIIa presenting as non-ketotic hypoglycemia: use of a newly approved commercially available mutation analysis to non-invasively confirm the diagnosis.

Seigel J, Weinstein DA, Hillman R, Colbert B, Matthews B, Bachrach B. Seigel J, et al. J Pediatr Endocrinol Metab. 2008 Jun;21(6):587-90. J Pediatr Endocrinol Metab. 2008. PMID: 18717245

8

An adult case of glycogen storage disease type IIIa.

Kim KO, Lee HJ, Choi JW, Eun JR, Choi JH. Kim KO, et al. Korean J Hepatol. 2008 Jun;14(2):219-25. doi: 10.3350/kjhep.2008.14.2.219. Korean J Hepatol. 2008. PMID: 18617770

9

A Japanese patient with cardiomyopathy caused by a novel mutation R285X in the AGL gene.

Ogimoto A, Okubo M, Okayama H, Shin YS, Endo Y, Ebara T, Inoue K, Ohtsuka T, Tahara H, Murase T, Higaki J. Ogimoto A, et al. Circ J. 2007 Oct;71(10):1653-6. doi: 10.1253/circj.71.1653. Circ J. 2007. PMID: 17895567 Free article.

10

Glycogen storage disease type IIIa in curly-coated retrievers.

Gregory BL, Shelton GD, Bali DS, Chen YT, Fyfe JC. Gregory BL, et al. J Vet Intern Med. 2007 Jan-Feb;21(1):40-6. doi: 10.1892/0891-6640(2007)21[40:gsdtii]2.0.co;2. J Vet Intern Med. 2007. PMID: 17338148 Free article.

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