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Journal of Neurochemistry|June 1, 1995
Monoaminergic effects of folinic acid, L-DOPA, and 5-hydroxytryptophan in dihydropteridine reductase deficiencyD S Goldstein, S H Hahn, C Holmes, et al.Physical Review Letters|May 28, 2013
Physics of stimulated L→H transitionsK Miki, P H Diamond, S-H Hahn, et al.Molecular Genetics and Metabolism|June 3, 2004
Rapid, comprehensive screening of the human medium chain acyl-CoA dehydrogenase geneJ T McKinney, N Longo, S H Hahn, et al.ASDC Journal of Dentistry for Children|July 31, 2001
In vivo rehardening of enamel eroded by a cola drinkJ W Kim, K T Jang, S H Lee, et al.AJR. American Journal of Roentgenology|August 23, 2000
MR arthrography of the labral capsular ligamentous complex in the shoulder: imaging variations and pitfallsY H Park, J Y Lee, S H Moon, et al.Human Mutation|April 29, 1998
Identification of three novel mutations and a high frequency of the Arg778Leu mutation in Korean patients with Wilson diseaseE K Kim, O J Yoo, K Y Song, et al.The Review of Scientific Instruments|July 10, 2021
Multi-chord IR-visible two-color interferometer on KSTARJune-Woo Juhn, K C Lee, T G Lee, et al.Yonsei Medical Journal|August 1, 1996
Linear and whorled nevoid hypermelanosis with delayed psychomotor developmentS Y Yim, I Y Lee, U W Rah, et al.The Journal of Pediatrics|August 4, 1999
Very long chain acyl coenzyme A dehydrogenase deficiency in a 5-month-old Korean boy: identification of a novel mutationS H Hahn, E H Lee, J W Jung, et al.Human Genetics|July 9, 2004
A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type IIJ W Kim, S H Nam, K T Jang, et al.Pageof 4