H. Kim

发表

Cytokines secreted by mesenchymal stem cells reduce demyelination in an animal model of Charcot-Marie-Tooth disease.

Myoung-Woo Lee, H. Jeon, H. Kim, 2022, Biochemical and biophysical research communications.

Charcot‐Marie‐Tooth Disease Type 4H Resulting from Compound Heterozygous Mutations in FGD4 from Nonconsanguineous Korean Families

Deok‐Ho Kim, H. Koo, H. Kim, 2015, Annals of human genetics.

Genetic and clinical spectrums in Korean Charcot‐Marie‐Tooth disease patients with myelin protein zero mutations

Ji Eun Lee, H. Kim, Byung-Ok Choi, 2021, Molecular genetics & genomic medicine.

Farnesol Ameliorates Demyelinating Phenotype in a Cellular and Animal Model of Charcot-Marie-Tooth Disease Type 1A

H. Kim, H. Doo, G. Kwak, 2021, Current issues in molecular biology.

ADSSL1 mutation relevant to autosomal recessive adolescent onset distal myopathy

Ji Eun Lee, H. Kim, Won Min Mo, 2016, Annals of neurology.

Phenotypic heterogeneity in patients with NEFL‐related Charcot–Marie–Tooth disease

H. Kim, Y. Hong, Hyun Su Kim, 2022, Molecular genetics & genomic medicine.

Clinical and Neuroimaging Features in Charcot-Marie-Tooth Patients with GDAP1 Mutations

H. Kim, Byung-Ok Choi, Hyun Su Kim, 2020, Journal of clinical neurology.

Analysis of Microsatellite Loci for Swimming Crab Portunus trituberculatus Populations in the Korean Side of the Yellow Sea

H. Kim, Y. S. Hyun, K. Chung, 2013 .

Compound heterozygous mutations of TYMP as underlying causes of mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).

Ji Hoon Park, H. Kim, Byung-Ok Choi, 2013, Molecular medicine reports.

Distal Myopathy with Rimmed Vacuoles Confirmed by Whole Exome Sequencing

Hyun Seok Song, H. Kim, Byung-Ok Choi, 2014 .

MPZ-, GDAP1-, and NEFL-Related Charcot-Marie-Tooth Disease with Diverse Clinical and Electrophysiological Phenotypes

H. Kim, Byung-Ok Choi, Sang Beom Kim, 2022, Journal of Electrodiagnosis and Neuromuscular Diseases.

Ser135Phe mutation in HSPB1 (HSP27) from Charcot–Marie–Tooth disease type 2F families

H. Kim, Byung-Ok Choi, Y. Hong, 2015, Genes & Genomics.

A novel INF2 mutation in a Korean family with autosomal dominant intermediate Charcot‐Marie‐Tooth disease and focal segmental glomerulosclerosis

H. Kim, Byung-Ok Choi, Y. Hong, 2014, Journal of the peripheral nervous system : JPNS.

Whole-genome sequencing in clinically diagnosed Charcot–Marie–Tooth disease undiagnosed by whole-exome sequencing

Hyemi Kwon, H. Kim, Ja-Hyun Jang, 2023, Brain communications.

Compound mitochondrial DNA mutations in a neurological patient with ataxia, myoclonus and deafness

H. Kim, Byung-Ok Choi, B. R. Yoon, 2014, Journal of Genetics.

miR-381 Attenuates Peripheral Neuropathic Phenotype Caused by Overexpression of PMP22

H. Kim, G. Kwak, Byung-Ok Choi, 2019, Experimental neurobiology.