Yang SH - Search Results

1

Atypical manifestation of carnitine palmitoyltransferase 1A deficiency: hepatosplenomegaly and nephromegaly.

Lee BH, Kim YM, Kim JH, Kim GH, Kim JM, Kim JH, Woo KH, Yang SH, Kim CJ, Choi IH, Yoo HW. Lee BH, et al. Among authors: yang sh. J Pediatr Gastroenterol Nutr. 2015 Mar;60(3):e19-22. doi: 10.1097/MPG.0b013e3182a95a42. J Pediatr Gastroenterol Nutr. 2015. PMID: 23969540 No abstract available.

2

Allele frequency of a 24 bp duplication in exon 10 of the CHIT1 gene in the general Korean population and in Korean patients with Gaucher disease.

Woo KH, Lee BH, Heo SH, Kim JM, Kim GH, Kim YM, Kim JH, Choi IH, Yang SH, Yoo HW. Woo KH, et al. Among authors: yang sh. J Hum Genet. 2014 May;59(5):276-9. doi: 10.1038/jhg.2014.16. Epub 2014 Mar 13. J Hum Genet. 2014. PMID: 24621582

3

Mutations of the GLA gene in Korean patients with Fabry disease and frequency of the E66Q allele as a functional variant in Korean newborns.

Lee BH, Heo SH, Kim GH, Park JY, Kim WS, Kang DH, Choe KH, Kim WH, Yang SH, Yoo HW. Lee BH, et al. Among authors: yang sh. J Hum Genet. 2010 Aug;55(8):512-7. doi: 10.1038/jhg.2010.58. Epub 2010 May 27. J Hum Genet. 2010. PMID: 20505683

4

Low prevalence of classical galactosemia in Korean population.

Lee BH, Cheon CK, Kim JM, Kang M, Kim JH, Yang SH, Kim GH, Choi JH, Yoo HW. Lee BH, et al. Among authors: yang sh. J Hum Genet. 2011 Jan;56(1):94-6. doi: 10.1038/jhg.2010.152. Epub 2010 Dec 9. J Hum Genet. 2011. PMID: 21150919

5

Maternal 3-methylcrotonyl-coenzyme A carboxylase deficiency with elevated 3-hydroxyisovalerylcarnitine in breast milk.

Cho KL, Kim YJ, Yang SH, Kim GH, Lee JH. Cho KL, et al. Among authors: yang sh. Korean J Pediatr. 2016 Nov;59(Suppl 1):S41-S44. doi: 10.3345/kjp.2016.59.11.S41. Epub 2016 Nov 30. Korean J Pediatr. 2016. PMID: 28018443 Free PMC article.

6

Evaluation of Serum Cotinine Cut-Off to Distinguish Smokers From Nonsmokers in the Korean Population.

Ko K, Kwon MJ, Yang SH, Moon CJ, Lee EH, Woo HY, Park H. Ko K, et al. Among authors: yang sh. Ann Lab Med. 2016 Sep;36(5):427-33. doi: 10.3343/alm.2016.36.5.427. Ann Lab Med. 2016. PMID: 27374707 Free PMC article.

7

Acromicric Dysplasia Caused by a Novel Heterozygous Mutation of FBN1 and Effects of Growth Hormone Treatment.

Jin HS, Song HY, Cho SY, Ki CS, Yang SH, Kim OH, Kim SJ. Jin HS, et al. Among authors: yang sh. Ann Lab Med. 2017 Jan;37(1):92-94. doi: 10.3343/alm.2017.37.1.92. Ann Lab Med. 2017. PMID: 27834076 Free PMC article. No abstract available.

8

Novel compound heterozygous mutations in the fructose-1,6-bisphosphatase gene cause hypoglycemia and lactic acidosis.

Moon S, Kim JH, Han JH, Ko SH, Ahn YB, Kim JH, Yang SH, Song KH. Moon S, et al. Among authors: yang sh. Metabolism. 2011 Jan;60(1):107-13. doi: 10.1016/j.metabol.2009.12.021. Epub 2010 Jan 25. Metabolism. 2011. PMID: 20096900

9

Effect of Light Regime on Candidatus Puniceispirillum marinum IMCC1322 in Nutrient-Replete Conditions.

Oh HM, Lee JH, Choi A, Yang SH, Shin GH, Kang SG, Cho JC, Kim HJ, Kwon KK. Oh HM, et al. Among authors: yang sh. J Microbiol Biotechnol. 2024 Nov 27;35:e2410034. doi: 10.4014/jmb.2410.10034. J Microbiol Biotechnol. 2024. PMID: 39809517 Free article.

10

Cholesterol-Lowering Activity of Lactiplantibacillus pentosus KS6I1 in High-Cholesterol Diet-Induced Hypercholesterolemic Mice.

Damodharan K, Palaniyandi SA, Yang SH, Balaji S. Damodharan K, et al. Among authors: yang sh. J Microbiol Biotechnol. 2024 Nov 21;35:e2404029. doi: 10.4014/jmb.2409.04029. J Microbiol Biotechnol. 2024. PMID: 39809508 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

2,881 results

Search Page

Filters