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A recurrent case of SCN4A related Paramyotonia congenita in two Korean brothers: a case report
Minsung Kang, Sohyeon Kim, Hyungseok Hah, Hung Youl Seok, Jin-Sung Park
Ann Clin Neurophysiol. 2024; 26(1): 22-25.   Published online March 25, 2024
doi: https://doi.org/10.14253/acn.23008
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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
doi: https://doi.org/10.14253/acn.2021.23.1.61
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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
doi: https://doi.org/10.14253/acn.2020.22.1.8
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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
doi: https://doi.org/10.14253/acn.2019.21.1.57
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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
doi: https://doi.org/10.14253/acn.2018.20.2.89
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