Purevsuren J - Search Results

1

Overview of Telemedicine Services in Mongolia.

Enkhmaa D, Munkhuu B, Baatar T, Purevsuren J, Minjuur E, Luuzanbadam G, MacKenzie R, Warburton D, Enkhtur S. Enkhmaa D, et al. Among authors: purevsuren j. Curr Pediatr Rep. 2021;9(3):77-82. doi: 10.1007/s40124-021-00245-w. Epub 2021 Jul 9. Curr Pediatr Rep. 2021. PMID: 34258106 Free PMC article. Review.

2

The first Mongolian cases of phenylketonuria in selective screening of inborn errors of metabolism.

Purevsuren J, Bolormaa B, Narantsetseg C, Batsolongo R, Enkhchimeg O, Bayalag M, Hasegawa Y, Shintaku H, SeijiYamaguchi. Purevsuren J, et al. Mol Genet Metab Rep. 2016 Oct 28;9:71-74. doi: 10.1016/j.ymgmr.2016.10.008. eCollection 2016 Dec. Mol Genet Metab Rep. 2016. PMID: 27830119 Free PMC article.

3

Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screening.

Shibata N, Hasegawa Y, Yamada K, Kobayashi H, Purevsuren J, Yang Y, Dung VC, Khanh NN, Verma IC, Bijarnia-Mahay S, Lee DH, Niu DM, Hoffmann GF, Shigematsu Y, Fukao T, Fukuda S, Taketani T, Yamaguchi S. Shibata N, et al. Among authors: purevsuren j. Mol Genet Metab Rep. 2018 May 21;16:5-10. doi: 10.1016/j.ymgmr.2018.05.003. eCollection 2018 Sep. Mol Genet Metab Rep. 2018. PMID: 29946514 Free PMC article.

4

Urinary organic metabolite screening of children with influenza-associated encephalopathy for inborn errors of metabolism using GC/MS.

Purevsuren J, Hasegawa Y, Kobayashi H, Endo M, Yamaguchi S. Purevsuren J, et al. Brain Dev. 2008 Sep;30(8):520-6. doi: 10.1016/j.braindev.2008.01.001. Epub 2008 Feb 11. Brain Dev. 2008. PMID: 18262742

5

Clinical and molecular aspects of Japanese patients with mitochondrial trifunctional protein deficiency.

Purevsuren J, Fukao T, Hasegawa Y, Kobayashi H, Li H, Mushimoto Y, Fukuda S, Yamaguchi S. Purevsuren J, et al. Mol Genet Metab. 2009 Dec;98(4):372-7. doi: 10.1016/j.ymgme.2009.07.011. Epub 2009 Jul 23. Mol Genet Metab. 2009. PMID: 19699128

6

Clinical and molecular investigation of 19 Japanese cases of glutaric acidemia type 1.

Mushimoto Y, Fukuda S, Hasegawa Y, Kobayashi H, Purevsuren J, Li H, Taketani T, Yamaguchi S. Mushimoto Y, et al. Among authors: purevsuren j. Mol Genet Metab. 2011 Mar;102(3):343-8. doi: 10.1016/j.ymgme.2010.11.159. Epub 2010 Nov 25. Mol Genet Metab. 2011. PMID: 21176883

7

Study of deep intronic sequence exonization in a Japanese neonate with a mitochondrial trifunctional protein deficiency.

Purevsuren J, Fukao T, Hasegawa Y, Fukuda S, Kobayashi H, Yamaguchi S. Purevsuren J, et al. Mol Genet Metab. 2008 Sep-Oct;95(1-2):46-51. doi: 10.1016/j.ymgme.2008.06.013. Epub 2008 Aug 9. Mol Genet Metab. 2008. PMID: 18693053

8

A novel molecular aspect of Japanese patients with medium-chain acyl-CoA dehydrogenase deficiency (MCADD): c.449-452delCTGA is a common mutation in Japanese patients with MCADD.

Purevsuren J, Kobayashi H, Hasegawa Y, Mushimoto Y, Li H, Fukuda S, Shigematsu Y, Fukao T, Yamaguchi S. Purevsuren J, et al. Mol Genet Metab. 2009 Feb;96(2):77-9. doi: 10.1016/j.ymgme.2008.10.012. Epub 2008 Dec 6. Mol Genet Metab. 2009. PMID: 19064330

9

Clinical and molecular aspects of Japanese children with medium chain acyl-CoA dehydrogenase deficiency.

Purevsuren J, Hasegawa Y, Fukuda S, Kobayashi H, Mushimoto Y, Yamada K, Takahashi T, Fukao T, Yamaguchi S. Purevsuren J, et al. Mol Genet Metab. 2012 Sep;107(1-2):237-40. doi: 10.1016/j.ymgme.2012.06.010. Epub 2012 Jun 26. Mol Genet Metab. 2012. PMID: 22796001

10

Bezafibrate can be a new treatment option for mitochondrial fatty acid oxidation disorders: evaluation by in vitro probe acylcarnitine assay.

Yamaguchi S, Li H, Purevsuren J, Yamada K, Furui M, Takahashi T, Mushimoto Y, Kobayashi H, Hasegawa Y, Taketani T, Fukao T, Fukuda S. Yamaguchi S, et al. Among authors: purevsuren j. Mol Genet Metab. 2012 Sep;107(1-2):87-91. doi: 10.1016/j.ymgme.2012.07.004. Epub 2012 Jul 14. Mol Genet Metab. 2012. PMID: 22841441

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