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Journal of the Neurological Sciences|August 14, 2012
Limb-girdle phenotype is frequent in patients with myopathy associated with GNE mutationsYoung-Eun Park, Hyang-Suk Kim, Eun-Suk Choi, et al.Acta Neurologica Scandinavica|June 4, 2005
Phenotypic variability in Kennedy's disease: implication of the early diagnostic featuresJae-Hyeok Lee, Jin-Hong Shin, Kyung-Pil Park, et al.Brain : a Journal of Neurology|May 31, 2022
Characteristics of spinal and bulbar muscular atrophy in South Korea: a cross-sectional study of 157 patientsHee-Jin Cho, Jin-Hong Shin, Young-Eun Park, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 25, 2013
Possible anticipation associated with a novel splice site mutation in episodic ataxia type 2Kwang-Dong Choi, Ji-Won Yook, Min-Ji Kim, et al.Journal of Korean Medical Science|December 2, 2009
Novel CLCN1 mutations and clinical features of Korean patients with myotonia congenitaIn-Soo Moon, Hyang-Sook Kim, Jin-Hong Shin, et al.Journal of Vestibular Research : Equilibrium & Orientation|December 8, 2020
Neutrophil-mediated immune response as a possible mechanism of acute unilateral vestibulopathyEun Hye Oh, Je-Keun Rhee, Jin-Hong Shin, et al.Frontiers in Neurology|February 11, 2020
Rare Variants of Putative Candidate Genes Associated With Sporadic Meniere's Disease in East Asian PopulationEun Hye Oh, Jin-Hong Shin, Hyang-Sook Kim, et al.Journal of Neuropathology and Experimental Neurology|October 19, 2017
Pathologic Correlation of Paramagnetic White Matter Lesions in Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented GliaMinkyeong Kim, Hansol Lee, Hyung Joon Cho, et al.Journal of Clinical Neurology (Seoul, Korea)|July 22, 2014
Mutation analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic ParaplegiaTae-Hyoung Kim, Jae-Hyeok Lee, Young-Eun Park, et al.Journal of the Neurological Sciences|December 17, 2017
Patterns and modulations of Pendular nystagmus in a family with hereditary spastic paraplegiaEun Hye Oh, Jae-Hyeok Lee, Jin-Hong Shin, et al.Pageof 11