• Kim Yoo-Mi

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 122 ~ 122

• Lee Jeong-Ho

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 119 ~ 121

• Pompe Disease: Long Term Management & Unmet Needs

• Ko Jung-Min

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 97 ~ 118

• Long-term Effectiveness of Enzyme Replacement Therapy in Fabry Disease

• Kim Ja-Hye

• Cho Ja-Hyang, Choi Jin-Ho, Leel Beom-Hee, Yoo Han-Wook

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 96 ~ 96

• Sohn Young-Bae

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 95 ~ 95

• Inborn Errors of Metabolism with Bony Manifestation

• Jin Dong-Kyu

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 94 ~ 94

• Shin Young-Lim

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 90 ~ 93

• Inborn Errors of Metabolism with Seizure Disorder and Neurologic Deficits

• Hwang Su-Kyeong

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 75 ~ 89

• Systematic Approach for the Diagnosis of IEM in the Neonatal Period

• Lee Hong-Jin

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 74 ~ 74

• Discovery of Tetrahydrobiopterin-responsive Phenylalanine Hydroxylase Deficiency

• Kure Shigeo

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 72 ~ 73

• The Past, Present, Future of Newborn Screening in Korea

• Lee Dong-Hwan

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 71 ~ 71

• A Case of Adrenoleukodystrophy Diagnosed as Hyponatremic Dehydration

• Lee Sang-Heon

• Kim Hyung-Jin, Kwon Young-Se, Kim Soon-Ki, Lee Ji-Eun

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 66 ~ 70

• A Case of Smith-Lemli-Opitz Syndrome in DHCR7 Mutation

• Jeong Yu-Ju

• Huh Rimm, Kwun Young-Hee, Lee Ji-Eun, Cho Sung-Yoon, Ki Chang-Seok, Jin Dong-Kyu

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 60 ~ 65

• A Case of Cerebral Adrenoleukodystrophy with c.1252C>T Mutation inABCD1 Gene

• Kim Yoo-Seon

• Huh Rimm, Kwun Young-Hee, Lee Ji-Eun, Cho Sung-Yoon, Ki Chang-Seok, Jin Dong-Kyu

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 54 ~ 59

• Clinical and Molecular Genetic Characteristics of Korean Patients with Smith-Lemli-Opitz Syndrome: A...

• Ko Jung-Min

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 48 ~ 53

• Longterm Benefit and Unmet Needs in Enzyme Replacement Therapy of Gaucher

• Kim Yoo-Mi

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 42 ~ 47

• Long-term Effectiveness of Enzyme Replacement Therapy in Fabry Disease

• Kim Ja-Hye

• Cho Ja-Hyang, Choi Jin-Ho, Leel Beom-Hee, Yoo Han-Wook

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 37 ~ 41

• Sohn Young-Bae

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 29 ~ 36

• Inborn Errors of Metabolism with Bony Manifestation

• Huh Rimm

• Cho Sung-Yoon, Jin Dong-Kyu

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 19 ~ 28

• Systematic Approach for the Diagnosis of IEM in the Neonatal Period

• Lee Hong-Jin

• Journal of the Korean Society of Inherited Metabolic Disease   2014  Volume.14  No.1 10 ~ 18