Sleep Related Problems as a Nonmotor Symptom of Dentatorubropallidoluysian Atrophy

por Kim, Hyeyun, Yun, Ji Young, Choi, Kyoung-Gyu, Koo, Heasoo, Han, Hyun Jeong
Publicado 2018

Zonal Difference and Prognostic Significance of Foxp3 Regulatory T Cell Infiltration in Breast Cancer

por Kim, Sewha, Lee, Anbok, Lim, Woosung, Park, Sanghui, Cho, Min Sun, Koo, Heasoo, Moon, Byung-In, Sung, Sun Hee
Publicado 2014

Recurrent Episodes of Rhabdomyolysis after Seizures in a Patient with Glycogen Storage Disease Type V

por Park, Hyung Jun, Chang, Yoonkyung, Lee, Jee Eun, Koo, Heasoo, Oh, Jeeyoung, Choi, Young-Chul, Park, Kee Duk
Publicado 2016

Novel Compound Heterozygous Nonsense PRX Mutations in a Korean Dejerine-Sottas Neuropathy Family

por Choi, Ye Ji, Hyun, Young Se, Nam, Soo Hyun, Koo, Heasoo, Hong, Young Bin, Chung, Ki Wha, Choi, Byung-Ok
Publicado 2015

Electron Microscopy Pathology of ADSSL1 Myopathy

por Park, Hyung Jun, Lee, Jee Eun, Choi, Gyeong Seon, Koo, Heasoo, Han, Soo Jeong, Yoo, Jeong Hyun, Choi, Young-Chul, Park, Kee Duk
Publicado 2017

Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1

por LEE, JINHO, JUNG, SUNG-CHUL, HONG, YOUNG BIN, YOO, JEONG HYUN, KOO, HEASOO, LEE, JA HYUN, HONG, HYUN DAE, KIM, SANG-BEOM, CHUNG, KI WHA, CHOI, BYUNG-OK
Publicado 2016

A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth disease

por Hong, Young Bin, Lee, Ja Hyun, Park, Jin-Mo, Choi, Yu-Ri, Hyun, Young Se, Yoon, Bo Ram, Yoo, Jeong Hyun, Koo, Heasoo, Jung, Sung-Chul, Chung, Ki Wha, Choi, Byung-Ok
Publicado 2013

Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease

por Kim, Hyeon Jin, Hong, Young Bin, Park, Jin-Mo, Choi, Yu-Ri, Kim, Ye Jin, Yoon, Bo Ram, Koo, Heasoo, Yoo, Jeong Hyun, Kim, Sang Beom, Park, Minhwa, Chung, Ki Wha, Choi, Byung-Ok
Publicado 2013

Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy

por Park, Mi-Hyun, Woo, Hae-Mi, Hong, Young Bin, Park, Ji Hoon, Yoon, Bo Ram, Park, Jin-Mo, Yoo, Jeong Hyun, Koo, Heasoo, Chae, Jong-Hee, Chung, Ki Wha, Choi, Byung-Ok, Koo, Soo Kyung
Publicado 2014

A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathy

por Choi, Yu-Ri, Hong, Young Bin, Jung, Sung-Chul, Lee, Ja Hyun, Kim, Ye Jin, Park, Hyung Jun, Lee, Jinho, Koo, Heasoo, Lee, Ji-Su, Jwa, Dong Hwan, Jung, Namhee, Woo, So-Youn, Kim, Sang-Beom, Chung, Ki Wha, Choi, Byung-Ok
Publicado 2015

A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy

por Hong, Young Bin, Joo, Jaesoon, Hyun, Young Se, Kwak, Geon, Choi, Yu-Ri, Yeo, Ha Kyung, Jwa, Dong Hwan, Kim, Eun Ja, Mo, Won Min, Nam, Soo Hyun, Kim, Sung Min, Yoo, Jeong Hyun, Koo, Heasoo, Park, Hwan Tae, Chung, Ki Wha, Choi, Byung-Ok
Publicado 2016