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| 1 |
Long-chain Fatty Acid Oxidation Disorders and Therapeutic Approach
Lee, Jung Hyun;
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The Korea Society of Inherited Metabolic Disease
, v.22, no.1, pp.1-8,
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| 2 |
Glutaric Aciduria Type I: The Newborn Screening Program Changes the Outcomes of the Disease
Kim, Su Jin;
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The Korea Society of Inherited Metabolic Disease
, v.22, no.1, pp.9-14,
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| 3 |
Neurological Outcome of Patients with Late-onset Ornithine Transcarbamylase Deficiency
Jang, Kyung Mi;Hwang, Su-Kyeong;
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The Korea Society of Inherited Metabolic Disease
, v.22, no.1, pp.15-20,
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| 4 |
Very Long Chain Acyl-coenzyme A Dehydrogenase Deficiency: A Review of Pathophysiology, Clinical Manifestations, Diagnosis, and Treatment
Kang, Seokjin;
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The Korea Society of Inherited Metabolic Disease
, v.22, no.1, pp.21-27,
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| 5 |
Plasma Amino Acid and Urine Organic Acid Analyses in Leigh Syndrome
Na, Ji-Hoon;Lee, Hyunjoo;Lee, Hae-in;Huh, Euira;Lee, Young-Mock;
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The Korea Society of Inherited Metabolic Disease
, v.22, no.1, pp.28-36,
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