• Plasma Amino Acid and Urine Organic Acid Analyses in Leigh Syndrome

• Na Ji-Hoon

• Lee Hyun-Joo, Lee Hae-In, Huh Eui-Ra, Lee Young-Mock

• Journal of the Korean Society of Inherited Metabolic Disease   2022  Volume.22  No.1 28 ~ 36

• Very Long Chain Acyl-coenzyme A Dehydrogenase Deficiency: A Review of Pathophysiology, Clinical Mani...

• Kang Seok-Jin

• Journal of the Korean Society of Inherited Metabolic Disease   2022  Volume.22  No.1 21 ~ 27

• Neurological Outcome of Patients with Late-onset Ornithine Transcarbamylase Deficiency

• Jang Kyung-Mi

• Hwang Su-Kyeong

• Journal of the Korean Society of Inherited Metabolic Disease   2022  Volume.22  No.1 15 ~ 20

• Glutaric Aciduria Type I: The Newborn Screening Program Changes the Outcomes of the Disease

• Kim Su-Jin

• Journal of the Korean Society of Inherited Metabolic Disease   2022  Volume.22  No.1 9 ~ 14

• Long-chain Fatty Acid Oxidation Disorders and Therapeutic Approach

• Lee Jung-Hyun

• Journal of the Korean Society of Inherited Metabolic Disease   2022  Volume.22  No.1 1 ~ 8