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Molecular Genetics & Genomic Medicine|April 7, 2021
Genetic and clinical spectrums in Korean Charcot-Marie-Tooth disease patients with myelin protein zero mutationsHye Jin Kim, Soo Hyun Nam, Hye Mi Kwon, et al.
Journal of the Peripheral Nervous System : JPNS|November 23, 2021
Variants of aminoacyl-tRNA synthetase genes in Charcot-Marie-Tooth disease: A Korean cohort studyDa Eun Nam, Jin Hee Park, Cho Eun Park, et al.
Molecular Genetics & Genomic Medicine|January 19, 2022
Phenotypic heterogeneity in patients with NEFL-related Charcot-Marie-Tooth diseaseHye Jin Kim, Sang Beom Kim, Hyun Su Kim, et al.
Tumori|May 5, 2010
Pilot study of stereotactic body radiotherapy for huge hepatocellular carcinoma unsuitable for other therapiesYoung-Joo Shin, Mi-Sook Kim, Seong Yul Yoo, et al.
Orphanet Journal of Rare Diseases|July 13, 2013
Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth diseaseHyeon Jin Kim, Young Bin Hong, Jin-Mo Park, et al.
Taehan Kan Hakhoe Chi = the Korean Journal of Hepatology|December 25, 2002
[Isolation and culture of pig hepatocyte in large scale for the application of bioartificial liver system]Yu Jeong Chung, Hyuk Joon Lee, Young Taeg Koh, et al.
Multiple Sclerosis and Related Disorders|June 5, 2020
Bone health in neuromyelitis optica: Bone mineral density and fracturesYoung Nam Kwon, Sun Young Im, Yong-Shik Park, et al.
BMC Neurology|October 7, 2015
A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathyYu-Ri Choi, Young Bin Hong, Sung-Chul Jung, et al.
Human Mutation|April 12, 2011
A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14Byung-Ok Choi, Sung Hee Kang, Young Se Hyun, et al.
Oncotarget|January 13, 2017
Association between metformin use and mortality in patients with type 2 diabetes mellitus and localized resectable pancreatic cancer: a nationwide population-based study in koreaWon Il Jang, Mi-Sook Kim, Shin Hee Kang, et al.
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