• A Case of Ornithine Transcarbamylase Deficiency in 11-month-old Female who Presented Periodic Vomiti...

• Kim Jin-Ah

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

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.3 165 ~ 170

• A Case of Hunter Syndrome Presented with Chronic Purulent Rhinorrhea in 24-month-old Boy

• Kim I-An

• Jin Jang-Yong, Park Jae-Ock, Hong Young-Hee

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.3 160 ~ 164

• An Infant Case of Citrin Deficiency with Corresponding Biochemical Features and a Heterozygous SLC25...

• Kang Su-Min

• Chi Yang-Hyun, Lee Jun-Hwa

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.3 155 ~ 159

• Ketolytic Defects in Children and Adolescents

• Choi Joon-Wan

• Ahn Seok-Min, Kim Young-Han, Baek Joon-Woo, Ryu Hye-Won, Bae Eun-Joo, Lee Hong-Jin

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.3 147 ~ 154

• A Rapid, Simple Determination of Sulfur-containing Compounds and Methylmalonic Acid on Plasma using ...

• Yoon Hye-Ran

• Maheshwor Thapa

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.3 138 ~ 146

• MicroRNA Expression Profiling in Cell and Mouse Models of Fabry Disease to Identify Biomarkers for F...

• Jung Nam-Hee

• Park Sae-Young, Jeon Yeo-Jin, Choi Yoon-Young, Jung Sung-Chul

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.3 127 ~ 137

• Long-term Follow-up of Patients with BH4 Deficiency in Korea

• Bang Hyun-Ho

• Lee Jeong-Ho, Lee Dong-Hwan

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.3 118 ~ 126

• Differential Diagnosis of Hyperphenylalaninemias

• Lee Jeong-Ho

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.3 110 ~ 117

• A Diagnostic Algorithm of Newborn Screening for Galactosemia

• Sohn Young-Bae

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.3 101 ~ 109

• 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

• A Clinically Diagnosed Case of Multiple Epiphyseal Dysplasia

• Kim Sun-Ja

• Cho Sung-Yoon, Kim Jin-Sup, Huh Rimm, Kwun Young-Hee, Lee Ji-Eun, Shim Jong-Sup, Kim ok-Hw...

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.1 49 ~ 54

• A Case Report for a Korean Patient with Mucopolysaccharidosis IIIA Confirmed by Biochemical and Mole...

• Kim Bo-Rahm

• Cho Sung-Yoon, Sohn Young-Bae, Park Hyung-Doo, Lee Soo-Youn, Song Jung-Han, Jin Dong-Kyu

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.1 44 ~ 48

• A Case of Short-chain Acyl-CoA Dehydrogenase Deficiency Detected by Newborn Screening

• Park Kyung-Won

• Ko Jung-Min, Jung Go-Un, Lee Hee-Chul, Yoon So-Young, Ko Sun-Young, Lee Yeon-Kyung, Shin S...

• Journal of the Korean Society of Inherited Metabolic Disease   2015  Volume.15  No.1 40 ~ 43