삼성서울병원

Ko En

신경과 최병옥 교수

진료분야
손발저림, 통증, 샤르코마리투스병, 루게릭병, 중증 근육무력증, 길랑-바레 증후군, 근육병, 척수질환
진료일정 12 月
날짜
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오전
오후
진료일정 01 月
날짜
01
02
03
04
05
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오전
오후

학력

학력
2001.02 연세대학교 의과대학원, 신경과학 박사
1996.02 연세대학교 의과대학원 석사
1989.02 연세대학교 의과대학 의학사

경력

경력
2018.01 ~현재 성균관대학교 의학연구소장
2018.01 ~현재 성균관대학교 의과대학 연구부학장
2018.01 ~현재 대한의학유전학회 임상유전학 인증의
2015.02 ~현재 성균관대학교 신경과 교수
2013.09 ~현재 보건복지부 신경계희귀질환 중개연구센터장
2009.03 ~현재 이화여자대학교 연구활성화위원
2005.01 ~현재 대한의사협회 교육위원
2012.05 ~ 2013.08 이화여자대학교 신경과 교수
2010.03 ~ 2013.08 대한근전도전기진단의학회 근전도 인증의
2008.12 ~ 2010.07 대한신경과학회 용어위원
2005.03 ~ 2010.02 한국희귀난치성질환연합회 이사
2005.11 ~ 2008.02 이화여자대학교 신경과 부교수
2004.05 ~ 2007.05 이화여자대학교 신경과 조교수
2003.01 ~ 2005.02 CHA의과대학 신경과 조교수
2000.05 ~ 2002.12 전임의
1993.03 ~ 2000.02 연세대학교 세브란스병원 신경과 전공의

학회활동

학회활동
2015.01 ~ 현재 대한신경근육질환학회 이사
2015.01 ~ 현재 대한의학유전학회 임원
2015.01 ~ 현재 대한근전도전기진단의학회 이사
2013.03 ~ 현재 대한퇴행성신경질환학회 이사
2003.01 ~ 현재 국제말초신경학회 회원 (PNS)
2000.10 ~ 현재 미국신경과학회 회원 (AAN)
2000.03 ~ 현재 대한근전도전기진단의학회 회원
1995.03 ~ 현재 대한신경과학회 회원

수상이력

수상이력
2014 연구자상 수상
2014 보건복지부 장관상 (우수연구자 부문) 수상
2014 대한의학유전학회
2012 국제학회 (ICNMD
2012 International Congress on Neuromuscular Disorder)
2010 우수발표상 수상
2008 우수논문상 수상
2008 대한근전도전기진단의학회
2007 대한치매학회
2006 대한신경과학회
2006 우수발표상 수상
2005 젊은연구자상 수상
2004 International Society of Hematology)
2002 국제학회 (ISH
  • BMC MED GENOMICS 2021 10.1186/s12920-021-01019-5 Novel homozygous mutations in Pakistani families with Charcot-Marie-Tooth disease Kanwal1, S; Choi, YJ; Lim, SO; Choi, HJ; Park, JH; Nuzhat, R; Khan, A; Perveen, S; Choi, BO; Chung, KW
    View PubMed
  • LIFE-BASEL 2021 10.3390/life11060494 Clinical and Neuroimaging Features in Charcot-Marie-Tooth Patients with GNB4 Mutations Kwon1, HM; Kim, HS; Kim, SB; Park, JH; Nam, DE; Lee, AJ; Nam, SH; Hwang, S; Chung, KW; Choi, BO
    View PubMed
  • MOL GENET GENOM MED 2021 10.1002/mgg3.1678 Genetic and clinical spectrums in Korean Charcot-Marie-Tooth disease patients with myelin protein zero mutations Kim1, HJ; Nam, SH; Kwon, HM; Lim, SO; Park, JH; Kim, HS; Kim, SB; Lee, KS; Lee, JE; Choi, BO; Chung, KW
    View PubMed
  • ANIM CELLS SYST 2021 10.1080/19768354.2021.1880967 Gait parameters as tools for analyzing phenotypic alterations of a mouse model of Charcot-Marie-Tooth disease Hwang1, SH; Chang, EH; Kwak, G; Jeon, H; Choi, BO; Hong, YB
    View PubMed
  • J CLIN NEUROL 2021 10.3988/jcn.2021.17.1.52 Clinical and Neuroimaging Features in Charcot-Marie-Tooth Patients with GDAP1 Mutations Kim1, HS; Kim, HJ; Nam, SH; Kim, SB; Choi, YJ; Lee, KS; Chung, KW; Yoon, YC; Choi, BO
    View PubMed
  • MOL MED REP 2020 10.3892/mmr.2020.11579 Short hairpin RNA treatment improves gait in a mouse model of Charcot-Marie-Tooth disease type 1A Doo1, HM; Hong, YB; Han, J; Moon, HW; Hwang, H; Kwak, G; Nam, SH; Kim, SB; Chung, KW; Kim, JH; Choi, BO
    View PubMed
  • J NEUROENG REHABIL 2020 10.1186/s12984-020-00777-0 Wearable hip-assist robot modulates cortical activation during gait in stroke patients a functional near-infrared spectroscopy study Lee1, SH; Lee, HJ; Shim, Y; Chang, WH; Choi, BO; Ryu, GH; Kim, YH
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  • STEM CELLS 2020 10.1002/stem.3287 Fibulin 5, a human Wharton's jelly-derived mesenchymal stem cells-secreted paracrine factor, attenuates peripheral nervous system myelination defects through the Integrin-RAC1 signaling axis Won1, SY; Kwon, S; Jeong, HS; Chung, KW; Choi, BO; Chang, JW; Lee, JE
    View PubMed
  • EUR RADIOL 2020 10.1007/s00330-020-07435-y Texture analysis using T1-weighted images for muscles in Charcot-Marie-Tooth disease patients and volunteers Lee1, JH; Yoon, YC; Kim, HS; Kim, JH; Choi, BO
    View PubMed
  • BRIT J PHARMACOL 2020 10.1111/bph.15231 A novel histone deacetylase 6 inhibitor improves myelination of Schwann cells in a model of Charcot-Marie-Tooth disease type 1A Ha1, N; Choi, YI; Jung, N; Song, JY; Bae, DK; Kim, MC; Lee, YJ; Song, H; Kwak, G; Jeong, S; Park, S; Nam, SH; Jung, SC; Choi, BO
    View PubMed
  • MOL GENET GENOM MED 2020 10.1002/mgg3.1380 Paternal gender specificity and mild phenotypes in Charcot-Marie-Tooth type 1A patients with de novo 17p12 rearrangements Lee1, AJ; Nam, D; Choi, YJ; Noh, SW; Nam, SH; Lee, HJ; Kim, SJ; Song, GJ; Choi, BO; Chung, KW
    View PubMed
  • GENES GENOM 2020 10.1007/s13258-020-00933-9 Alanyl-tRNA synthetase 1 (AARS1) gene mutation in a family with intermediate Charcot-Marie-Tooth neuropathy Lee1, AJ; Nam, DE; Choi, YJ; Nam, SH; Choi, BO; Chung, KW
    View PubMed
  • GLIA 2020 10.1002/glia.23805 Loss-of-function of EBP50 is a new cause of hereditary peripheral neuropathy: EBP50 functions in peripheral nerve system Song1, GJ; Gupta, DP; Rahman, MH; Park, HT; Al Ghouleh, I; Bisello, A; Lee, MG; Park, JY; Park, HH; Jun, JH; Chung, KW; Choi, BO; Suk, K
    View PubMed
  • EMBO REP 2020 10.15252/embr.201948290 CEP41-mediated ciliary tubulin glutamylation drives angiogenesis through AURKA-dependent deciliation Ki1, SM; Kim, JH; Won, SY; Oh, SJ; Lee, IY; Bae, YK; Chung, KW; Choi, BO; Park, B; Choi, EJ; Lee, JE
    View PubMed
  • NUCLEIC ACIDS RES 2020 10.1093/nar/gkz1070 Targeted PMP22 TATA-box editing by CRISPR/Cas9 reduces demyelinating neuropathy of Charcot-Marie-Tooth disease type 1A in mice Lee1, JS; Lee, JY; Song, DW; Bae, HS; Doo, HM; Yu, HS; Lee, KJ; Kim, HK; Hwang, H; Kwak, G; Kim, D; Kim, S; Hong, YB; Lee, JM; Choi, BO
    View PubMed
  • BIOCHEM BIOPH RES CO 2020 10.1016/j.bbrc.2019.10.110 Human HSPB1 mutation recapitulates features of distal hereditary motor neuropathy (dHMN) in Drosophila Kang1, KH; Han, JE; Hong, YB; Nam, SH; Choi, BO; Koh, H
    View PubMed
  • Neurogenetics/ 2019 Aug;20(3):117-127 Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family Tey S11, Shahrizaila N2, Drew AP3,4, Samulong S1, Goh KJ2, Battaloglu E5, Atkinson D6, Parman Y7, Jordanova A6, Chung KW8, Choi BO9, Li YC10, Auer-Grumbach M11, Nicholson GA3,4,12, Kennerson ML13,14,15, Ahmad-Annuar A16.
    View PubMed
  • Genes & genomics / 2019 Sep;41(9):993-1000 Zebrafish is a central model to dissect the peripheral neuropathy Won SY11, Choi BO2, Chung KW3, Lee JE4,5.
    View PubMed
  • Annals of clinical and translational neurology / 2019 Jul;6(7):1292-1301 p75 and neural cell adhesion molecule 1 can identify pathologic Schwann cells in peripheral neuropathies Kim YH11, Kim YH2, Shin YK1, Jo YR1, Park DK2, Song MY2, Yoon BA1,3, Nam SH4, Kim JH5, Choi BO4,6, Shin HY7, Kim SW7, Kim SH8, Hong YB9, Kim JK1,3, Park HT1,10.
    View PubMed
  • Stroke / 2019 Dec;50(12):3545-3552 Training for Walking Efficiency With a Wearable Hip-Assist Robot in Patients With Stroke: A Pilot Randomized Controlled Trial Lee HJ11,2, Lee SH1, Seo K3, Lee M3, Chang WH1, Choi BO4, Ryu GH5, Kim YH1,6.
    View PubMed
  • Scientific reports / 2019 Nov 11;9(1):16535 Serum CXCL13 reflects local B-cell mediated inflammatory demyelinating peripheral neuropathy Kim YH11, Jang SY1, Shin YK1, Jo YR1, Yoon BA1,2,3, Nam SH4, Choi BO4,5, Shin HY6, Kim SW6, Kim SH7, Kim JK8,9, Park HT10,11.
    View PubMed
  • Journal of cachexia, sarcopenia and muscle / 2019 Jun;10(3):574-585 Muscle fat quantification using magnetic resonance imaging: case-control study of Charcot-Marie-Tooth disease patients and volunteers Kim HS11, Yoon YC1, Choi BO2, Jin W3, Cha JG4
    View PubMed
  • Annals of neurology/ 2019 Jul;86(1):55-67 A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs). Pareyson D11, Stojkovic T2, Reilly MM3, Leonard-Louis S2, Laur? M3, Blake J3,4, Parman Y5, Battaloglu E6, Tazir M7, Bellatache M7, Bonello-Palot N8, L?vy N8, Sacconi S9, Guimar?es-Costa R2, Attarian S10, Latour P11, Sol? G12, Megarbane A13,14, Horvath R15,16, Ricci G15,17, Choi BO18, Schenone A19, Gemelli C19, Geroldi A19, Sabatelli M20,21, Luigetti M21,22, Santoro L23, Manganelli F23, Quattrone A24, Valentino P24, Murakami T25, Scherer SS26, Dankwa L26, Shy ME27, Bacon CJ27, Herrmann DN28, Zambon A29, Tramacere I30, Pisciotta C1, Magri S31, Previtali SC29, Bolino A29.
    View PubMed
  • Journal of neuromuscular diseases / 2019;6(2):201-211 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study Tao F11, Beecham GW1, Rebelo AP1, Blanton SH1, Moran JJ2, Lopez-Anido C2, Svaren J2, Abreu L1, Rizzo D3, Kirk CA3, Wu X4, Feely S4, Verhamme C5, Saporta MA6, Herrmann DN7, Day JW8, Sumner CJ9,10, Lloyd TE9,10, Li J11, Yum SW12, Taroni F13, Baas F14, Choi BO15, Pareyson D13, Scherer SS16, Reilly MM17, Shy ME4, Z?chner S1; Inherited Neuropathy Consortium.
    View PubMed
  • STROKE 2019 10.1161/STROKEAHA.119.025950 Training for Walking Efficiency With a Wearable Hip-Assist Robot in Patients With Stroke: A Pilot Randomized Controlled Trial Lee1, HJ; Lee, SH; Seo, K; Lee, M; Chang, WH; Choi, BO; Ryu, GH; Kim, YH
    View PubMed
  • SCI REP-UK 2019 10.1038/s41598-019-52643-2 Serum CXCL13 reflects local B-cell mediated inflammatory demyelinating peripheral neuropathy Kim1, YH; Jang, SY; Shin, YK; Jo, YR; Yoon, BA; Nam, SH; Choi, BO; Shin, HY; Kim, SW; Kim, SH; Kim, JK; Park, HT
    View PubMed
  • J HUM GENET 2019 10.1038/s10038-019-0636-y Compound heterozygous mutations of SH3TC2 in Charcot-Marie-Tooth disease type 4C patients Lee1, AJ; Nam, SH; Park, JM; Kanwal, S; Choi, YJ; Lee, HJ; Lee, KS; Lee, JE; Park, JS; Choi, BO; Chung, KW
    View PubMed
  • ACTA BIOMATER 2019 10.1016/j.actbio.2018.12.011 Nanotopographical regulation of pancreatic islet-like cluster formation from human pluripotent stem cells using a gradient-pattern chip Kim1, JH; Park, BG; Kim, SK; Lee, DH; Lee, GG; Kim, DH; Choi, BO; Lee, KB; Kim, JH
    View PubMed
  • GENES GENOM 2019 10.1007/s13258-019-00838-2 Zebrafish is a central model to dissect the peripheral neuropathy Won1, SY; Choi, BO; Chung, KW; Lee, JE
    View PubMed
  • NEUROGENETICS 2019 10.1007/s10048-019-00576-3 Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family Tey1, S; Shahrizaila, N; Drew, AP; Samulong, S; Goh, KJ; Battaloglu, E; Atkinson, D; Parman, Y; Jordanova, A; Chung, KW; Choi, BO; Li, YC; Auer-Grumbach, M; Nicholson, GA; Kennerson, ML; Ahmad-Annuar, A
    View PubMed
  • ANN CLIN TRANSL NEUR 2019 10.1002/acn3.50828 p75 and neural cell adhesion molecule 1 can identify pathologic Schwann cells in peripheral neuropathies Kim1, YH; Kim, YH; Shin, YK; Jo, YR; Park, DK; Song, MY; Yoon, BA; Nam, SH; Kim, JH; Choi, BO; Shin, H; Kim, SW; Kim, SH; Hong, YB; Kim, JK; Park, HT
    View PubMed
  • ANN NEUROL 2019 10.1002/ana.25500 A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs) Pareyson1, D; Stojkovic, T; Reilly, MM; Leonard-Louis, S; Laura, M; Blake, J; Parman, Y; Battaloglu, E; Tazir, M; Bellatache, M; Bonello-Palot, N; Levy, N; Sacconi, S; Guimaraes-Costa, R; Attarian, S; Latour, P; Sole, G; Megarbane, A; Horvath, R; Ricci, G; Choi, BO; Schenone, A; Gemelli, C; Geroldi, A; Sabatelli, M; Luigetti, M; Santoro, L; Manganelli, F; Quattrone, A; Valentino, P; Murakami, T; Scherer, SS; Dankwa, L; Shy, ME; Bacon, CJ; Herrmann, DN; Zambon, A; Tramacere, I; Pisciotta, C; Magri, S; Previtali, SC; Bolino, A
    View PubMed
  • INT J MOL MED 2019 10.3892/ijmm.2019.4178 Aminosalicylic acid reduces ER stress and Schwann cell death induced by MPZ mutations Chang1, EH; Mo, WM; Doo, HM; Lee, JS; Park, HT; Choi, BO; Hong, YB
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  • J CLIN NEUROL 2019 10.3988/jcn.2019.15.3.418 A POLG2 Homozygous Mutation in an Autosomal Recessive Epilepsy Family Without Ophthalmoplegia Lee1, SJ; Kanwal, S; Yoo, DH; Park, HR; Choi, BO; Chung, KW
    View PubMed
  • J CACHEXIA SARCOPENIA MUSCLE 2019 10.1002/jcsm.12415 Muscle fat quantification using magnetic resonance imaging: case-control study of Charcot-Marie-Tooth disease patients and volunteers Kim1, HS; Yoon, YC; Choi, BO; Jin, W; Cha, JG
    View PubMed
  • EUR RADIOL 2019 10.1007/s00330-018-5958-1 Diffusion tensor imaging of the sciatic nerve in Charcot-Marie-Tooth disease type I patients: a prospective case-control study Kim1, HS; Yoon, YC; Choi, BO; Jin, W; Cha, JG; Kim, JH
    View PubMed
  • Exp Neurobiol 2019 10.5607/en.2019.28.2.279 miR-381 Attenuates Peripheral Neuropathic Phenotype Caused by Overexpression of PMP22 Lee1, JS; Kwak, G; Kim, HJ; Park, HT; Choi, BO; Hong, YB
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  • ANN NEUROL 2019 10.1002/ana.25426 Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1A Tao1, FF; Beecham, GW; Rebelo, AP; Svaren, J; Blanton, SH; Moran, JJ; Lopez-Anido, C; Morrow, JM; Abreu, L; Rizzo, D; Kirk, CA; Wu, XY; Feely, S; Verhamme, C; Saporta, MA; Herrmann, DN; Day, JW; Sumner, CJ; Lloyd, TE; Li, J; Yum, SW; Taroni, F; Baas, F; Choi, BO; Pareyson, D; Scherer, SS; Reilly, MM; Shy, ME; Zuchner, S; Lewis, R; Acsadi, G; Finkel, R; Fridman, V; Ramchandren, S; Walk, D; Logigian, E; Stanton, M; Eichinger, K; Guntrum, D; Gibson, C; Burns, J; Moroni, I; Pisciotta, C; Laura, M; Muntoni, F; Sowden, JE; Mountain, J; Bai, YH; Bacon, C; Gutmann, L; Grider, T; Phetteplace, J; Seyedsadjadi, R; Houlden, H; Cortese, A; Pandraud, A; Calabrese, D; Saveri, P; Richardson, J; Dankwa, L; Lee, D; Siskind, C; Maciel, R; Bis, D
    View PubMed
  • NEUROMUSCULAR DISORD 2019 Replication studies of MIR149 association in Charcot-Marie-Tooth disease type 1A in a European population - response Choi1, BO; Nam, SH; Chung, KW
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  • American journal of human genetics / 2018 Mar 1;102(3):505-514 Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2. Lassuthova P11, Rebelo AP2, Ravenscroft G3, Lamont PJ4, Davis MR5, Manganelli F6, Feely SM7, Bacon C7, Bro?kov? D?1, Haberlova J8, Mazanec R9, Tao F2, Saghira C2, Abreu L2, Courel S2, Powell E10, Buglo E2, Bis DM2, Baxter MF3, Ong RW3, Marns L5, Lee YC11, Bai Y7, Isom DG12, Barro-Soria R13, Chung KW14, Scherer SS15, Larsson HP13, Laing NG3, Choi BO16, Seeman P1, Shy ME7, Santoro L6, Zuchner S17.
    View PubMed
  • GENES GENOM 2018 10.1007/s13258-018-0721-1 BAG3 mutation in a patient with atypical phenotypes of myofibrillar myopathy and Charcot-Marie-Tooth disease Kim1, SJ; Nam, SH; Kanwal, S; Nam, DE; Yoo, DH; Chae, JH; Suh, YL; Chung, KW; Choi, BO
    View PubMed
  • J CLIN NEUROL 2018 10.3988/jcn.2018.14.4.591 A Novel Nonsense Mutation in Leucine-Rich, Glioma-Inactivated-1 Gene as the Underlying Cause of Familial Temporal Lobe Epilepsy Kanwal1, S; Yoo, DH; Tahir, S; Lee, SJ; Lee, MH; Choi, BO; Chung, KW
    View PubMed
  • BMC Geriatr 2018 10.1186/s12877-018-0921-1 A wearable hip-assist robot reduces the cardiopulmonary metabolic energy expenditure during stair ascent in elderly adults: a pilot cross-sectional study Kim1, DS; Lee, HJ; Lee, SH; Chang, WH; Jang, J; Choi, BO; Ryu, GH; Kim, YH
    View PubMed
  • INT J MOL SCI 2018 10.3390/ijms19082393 Differentiation of Human Tonsil-Derived Mesenchymal Stem Cells into Schwann-Like Cells Improves Neuromuscular Function in a Mouse Model of Charcot-Marie-Tooth Disease Type 1A Park1, S; Jung, N; Myung, S; Choi, Y; Chung, KW; Choi, BO; Jung, SC
    View PubMed
  • SCI REP-UK 2018 10.1038/s41598-018-28501-y Hidden hearing loss in patients with Charcot-Marie-Tooth disease type 1A Choi1, JE; Seok, JM; Ahn, J; Ji, YS; Lee, KM; Hong, SH; Choi, BO; Moon, IJ
    View PubMed
  • NEUROMUSCULAR DISORD 2018 10.1016/j.nmd.2018.04.002 Association of miR-149 polymorphism with onset age and severity in Charcot-Marie-Tooth disease type 1A Nam1, SH; Kanwal, S; Nam, DE; Lee, MH; Kang, TH; Jung, SC; Choi, BO; Chung, KW
    View PubMed
  • J PERIPHER NERV SYST 2018 10.1111/jns.12249 Small heat shock protein B3 (HSPB3) mutation in an axonal Charcot-Marie-Tooth disease family Nam1, DE; Nam, SH; Lee, AJ; Hong, YB; Choi, BO; Chung, KW
    View PubMed
  • MUSCLE NERVE 2018 10.1002/mus.25763 Application of differentiated human tonsil-derived stem cells to trembler-J mice Park1, S; Choi, Y; Kwak, G; Hong, YB; Jung, N; Kim, J; Choi, BO; Jung, SC
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  • AM J HUM GENET 2018 10.1016/j.ajhg.2018.01.023 Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2 Lassuthova1, P; Rebelo, AP; Ravenscroft, G; Lamont, PJ; Davis, MR; Manganelli, F; Feely, SM; Bacon, C; Brozkova, DS; Haberlova, J; Mazanec, R; Tao, FF; Saghira, C; Abreu, L; Courel, S; Powell, E; Buglo, E; Bis, DM; Baxter, MF; Ong, RW; Marns, L; Lee, YC; Bai, YH; Isom, DG; Barro-Soria, R; Chung, KW; Scherer, SS; Larsson, HP; Laing, NG; Choi, BO; Seeman, P; Shy, ME; Santoro, L; Zuchner, S
    View PubMed
  • GENES GENOM 2018 10.1007/s13258-017-0612-x Wide phenotypic spectrum in axonal Charcot-Marie-Tooth neuropathy type 2 patients with KIF5A mutations Nam1, DE; Yoo, DH; Choi, SS; Choi, BO; Chung, KW
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  • J NEUROENG REHABIL 2017 10.1186/s12984-017-0333-z Gait performance and foot pressure distribution during wearable robot-assisted gait in elderly adults Lee1, SH; Lee, HJ; Chang, WH; Choi, BO; Lee, J; Kim, J; Ryu, GH; Kim, YH
    View PubMed
  • J PERIPHER NERV SYST 2017 10.1111/jns.12217 Clinical characterization and genetic analysis of Korean patients with X-linked Charcot-Marie-Tooth disease type 1 Hong1, YB; Park, JM; Yu, JS; Yoo, DH; Nam, DE; Park, HJ; Lee, JS; Hwang, SH; Chung, KW; Choi, BO
    View PubMed
  • IEEE T NEUR SYS REH 2017 10.1109/TNSRE.2017.2664801 A Wearable Hip Assist Robot Can Improve Gait Function and Cardiopulmonary Metabolic Efficiency in Elderly Adults Lee1, HJ; Lee, S; Chang, WH; Seo, K; Shim, Y; Choi, BO; Ryu, GH; Kim, YH
    View PubMed
  • J PERIPHER NERV SYST 2017 10.1111/jns.12223 Axonal Charcot-Marie-Tooth neuropathy concurrent with distal and proximal weakness by translational elongation of the 3 ' UTR in NEFH Nam1, DE; Jung, SC; Yoo, DH; Choi, SS; Seo, SY; Kim, GH; Kim, SJ; Nam, SH; Choi, BO; Chung, KW
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