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Adrenomyeloneuropathy with cerebral involvement due to a novel frameshift variant in ABCD1 gene   
Hye Weon Kim, Hyunjin Kim, Dongyoung Jeong, Kyuyoon Chung, Eun-Jae Lee, Young-Min Lim, Kwang-Kuk Kim
Ann Clin Neurophysiol. 2021; 23(1): 61-64.   Published online April 29, 2021
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Insight into the prognostic factors of chronic inflammatory demyelinating polyneuropathy   
Seol-Hee Baek
Ann Clin Neurophysiol. 2020; 22(1): 8-12.   Published online April 30, 2020
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A novel p.Leu699Pro mutation in MFN2 gene causes Charcot-Marie-Tooth disease type 2A   
Sa-Yoon Kang, Keun Hyuk Ko, Jung-Hwan Oh
Ann Clin Neurophysiol. 2019; 21(1): 57-60.   Published online January 29, 2019
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Novel recessive mutations of COL6A1 identified in the early severe phenotype of ullrich congenital muscular dystrophy   
Young-Eun Park, Jin-Hong Shin, Hyang-Sook Kim, Dae-Seong Kim
Ann Clin Neurophysiol. 2018; 20(2): 89-92.   Published online July 31, 2018
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