• A Case of asymptomatic Short-chain Acyl-CoA Dehydrogenase Deficiency

• Lee Hwa-Pyung

• Kim Jin-Sup, Huh Rimm, Cho Sung-Yoon, Jin Dong-Kyu

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.2 98 ~ 100

• Short-chain Acyl-CoA Dehydrogenase Deficiency in an Asymptomatic Neonate

• Lee Yeon-Hee

• Kim Jin-Sup, Huh Rimm, Cho Sung-Yoon, Jin Dong-Kyu

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.2 93 ~ 97

• A Case of Mucopolysaccharidosis Type 2 Diagnosed Early through Brain MRI

• Lee Yoon-Kyoung

• Cho Sung-Yoon, Kim Jin-Sup, Huh Rimm, Jin Dong-Kyu

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.2 87 ~ 92

• Clinical Features and Genetic Analysis of Homocystinuria Patients in Korea

• Lee Ye-Na

• Lee Jeong-Ho, Lee Dong-Hwan

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.2 78 ~ 86

• Clinical and Biochemical Diagnosis in Children with Leigh Syndrome

• Lee Sun-Ho

• Jeon Mi-Na, Lee Hyun-Joo, Park Dae-Young, Kim Se-Hoon, Lee Young-Mock

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.2 72 ~ 77

• Diagnostic Method for Inborn Metabolic Disorders using differentiation between D- and R- Isomers on ...

• Yoon Hye-Ran

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.2 65 ~ 71

• Simultaneous Quantification of Urinary L-, and D-Lactate by Reversed-Phase Liquid Chromatography Tan...

• Moon Chul-Jin

• Yang Song-Hyun

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.2 59 ~ 64

• Role of Tetrahydrobiopterin (BH4) Therapy in PKU

• Shintaku Haruo

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.2 55 ~ 58