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전체 논문

190

121

Pmp22 mutant allele-specific siRNA alleviates demyelinating neuropathic phenotype in vivo
Lee, JS (Lee, Ji-Su), Chang, EH (Chang, Eun Hyuk), Koo, OJ (Koo, Ok Jae), Jwa, DH (Jwa, Dong Hwan), Mo, WM (Mo, Won Min), Kwak, G (Kwak, Geon), Moon, HW (Moon, Hyo Won), Park, HT (Park, Hwan Tae), Hong, YB (Hong, Young Bin), Choi, BO (Choi, Byung-Ok)
NEUROBIOLOGY OF DISEASE, 2017

122

Cerebral white matter abnormalities in patients with charcot-marie-tooth disease
Lee, M (Lee, Mina), Park, CH (Park, Chang-hyun), Chung, HK (Chung, Hwa-Kyung), Kim, HJ (Kim, Hyeon Jin), Choi, Y (Choi, Yunseo), Yoo, JH (Yoo, Jeong Hyun), Yoon, YC (Yoon, Young Chul), Bin Hong, Y (Hong, Young Bin), Chung, KW (Chung, Ki Wha), Choi, BO (Choi, Byung-Ok), Lee, HW (Lee, Hyang Woon)...Mo
ANNALS OF NEUROLOGY, 2017

123

A longitudinal clinicopathological study of two unrelated patients with Charcot-Marie-Tooth disease type 1E
Kim J.Y., Kim S.-H., Park J.-Y., Koo H., Park K.-D., Hong Y.B., Chung K.W., Chot B.-O.
Neurology India, 2017

124

Tonsil-Derived Mesenchymal Stem Cells Differentiate into a Schwann Cell Phenotype and Promote Peripheral Nerve Regeneration
Jung, N (Jung, Namhee), Park, S (Park, Saeyoung), Choi, Y (Choi, Yoonyoung), Park, JW (Park, Joo-Won), Bin Hong, Y (Bin Hong, Young), Park, HHC (Park, Hyun Ho Choi), Yu, Y (Yu, Yeonsil), Kwak, G (Kwak, Geon), Kim, HS (Kim, Han Su), Ryu, KH (Ryu, Kyung-Ha), Kim, JK (Kim, Jae Kwang), Jo, I (Jo, Inho), Choi, BO (Choi, Byung-Ok), Jung, SC (Jung, Sung-Chul)...M
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016

125

Distal hereditary motor neuropathy type 7B with Dynactin 1 mutation
Hwang, SH (Hwang, Sun Hee), Kim, EJ (Kim, Eun Ja), Hong, YB (Hong, Young Bin), Joo, J (Joo, Jaesoon), Kim, SM (Kim, Sung Min), Nam, SH (Nam, Soo Hyun), Hong, HD (Hong, Hyun Dae), Kim, SH (Kim, Seung Hyun), Oh, K (Oh, Kiwook), Lim, JG (Lim, Jeong-Geun), Cho, JH (Cho, Jeong Hee), Chung, KW (Chung, Ki Wha), Choi, BO (Choi, Byung-Ok)...Mo
MOLECULAR MEDICINE REPORTS, 2016

126

Clinico-genetics in Korean Charcot-Marie-Tooth disease type 2Z with MORC2 mutations
Hyun, YS (Hyun, Young Se), Hong, YB (Hong, Young Bin), Choi, BO (Choi, Byung-Ok), Chung, KW (Chung, Ki Wha)
BRAIN, 2016

127

Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1
Lee, J (Lee, Jinho), Jung, SC (Jung, Sung-Chul), Hong, YB (Hong, Young Bin), Yoo, JH (Yoo, Jeong Hyun), Koo, H (Koo, Heasoo), Lee, JH (Lee, Ja Hyun), Hong, HD (Hong, Hyun Dae), Kim, SB (Kim, Sang-Beom), Chung, KW (Chung, Ki Wha), Choi, BO (Choi, Byung-Ok)
MOLECULAR MEDICINE REPORTS, 2016

128

ADSSL1 mutation relevant to autosomal recessive adolescent onset distal myopathy.
홍영빈
ANNALS OF NEUROLOGY, 2016

129

A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy.
홍영빈, 정기화, 최병옥, 주재순
PLOS GENETICS, 2016

130

DGAT2 Mutation in a Family with Autosomal Dominant Early-Onset Axonal Charcot-Marie-Tooth Disease.
홍영빈, 정기화, 최병옥
HUMAN MUTATION, 2016