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- CASK Mutation in an Infant with Microcephaly, Pontocerebellar Hypoplasia, and Hearing Loss
- Jun Chul Byun, Jung Sook Ha
- Ann Child Neurol. 2022;30(4):216-219. Published online September 22, 2022
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- A Case of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease with Acute Bilateral Total Blindness
- Jiyoon Ko, Ji-Hoon Na, Hyunjoo Lee, Jun Chul Byun, Joon Sik Kim, Young-Mock Lee
- Ann Child Neurol. 2022;30(4):197-200. Published online September 8, 2022
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- TSEN54 Gene-Related Pontocerebellar Hypoplasia Type 2 in a Newborn with Refractory Myoclonic Seizures
- Jun Chul Byun, Jung Sook Ha, Chun Soo Kim
- Ann Child Neurol. 2022;30(3):152-154. Published online June 28, 2022
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- A SERPINC1 Mutation in a Patient with Cerebral Venous Thrombosis and Upper-Extremity Deep Vein Thrombosis
- Jun Chul Byun, Jeong-Ho Hong
- Ann Child Neurol. 2022;30(3):134-136. Published online May 25, 2022
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- Clinical Characteristics of Epilepsy and Its Risk Factors in Neurofibromatosis Type 1: A Single-Center Study
- Areum Shin, Jun Chul Byun, Su-Kyeong Hwang, Soonhak Kwon, Yun Jeong Lee
- Ann Child Neurol. 2021;29(1):1-7. Published online December 28, 2020
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