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Clinical Neurology and Neurosurgery|October 20, 2020
Clinical characteristics of ataxia-telangiectasia presenting dystonia as a main manifestationMinkyeong Kim, Ah Reum Kim, Jongkyu Park, et al.Human Mutation|October 19, 2012
Destabilization and mislocalization of POU3F4 by C-terminal frameshift truncation and extension mutationByung Yoon Choi, Do-Hwan Kim, Taesu Chung, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 27, 2015
Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric populationNayoung K D Kim, Ah Reum Kim, Kyung Tae Park, et al.Journal of Movement Disorders|June 4, 2019
The Effect of Globus Pallidus Interna Deep Brain Stimulation on a Dystonia Patient with the GNAL Mutation Compared to Patients with DYT1 and DYT6Jong Hyeon Ahn, Ah Reum Kim, Nayoung K D Kim, et al.Journal of Translational Medicine|August 13, 2015
Strong founder effect of p.P240L in CDH23 in Koreans and its significant contribution to severe-to-profound nonsyndromic hearing loss in a Korean pediatric populationSo Young Kim, Ah Reum Kim, Nayoung K D Kim, et al.Molecules and Cells|August 6, 2015
Identification and Clinical Implications of Novel MYO15A Mutations in a Non-consanguineous Korean Family by Targeted Exome SequencingMun Young Chang, Ah Reum Kim, Nayoung K D Kim, et al.Parkinsonism & Related Disorders|September 22, 2020
Clarification of undiagnosed ataxia using whole-exome sequencing with clinical implicationsMinkyeong Kim, Ah Reum Kim, Ji Sun Kim, et al.Journal of Microbiology and Biotechnology|November 27, 2025
Upcycling of Adlay Bran via Lactobacillus Fermentation Enhances Anti-Melanogenic and Antioxidant Activities through MITF/Tyrosinase Pathway ModulationKyoung Mi Moon, Min-Kyeong Lee, Ji Yun Van, et al.Scientific Reports|May 14, 2026
Real-case applications of luminescence retrospective dosimetry in small-scale radiological accidentsHyoungtaek Kim, Hyungjoon Yu, Ah Reum Kim, et al.The Journal of Gene Medicine|November 26, 2016
Functional characterization of a novel loss-of-function mutation of PRPS1 related to early-onset progressive nonsyndromic hearing loss in Koreans (DFNX1): Potential implications on future therapeutic interventionSo Young Kim, Ah Reum Kim, Nayoung K D Kim, et al.Pageof 8