Repeated Intrathecal Mesenchymal Stem Cells for Amyotrophic Lateral Sclerosis von Oh, Ki‐Wook, Noh, Min‐Young, Kwon, Min‐Soo, Kim, Hyun Young, Oh, Seong‐il, Park, Jinseok, Kim, Hee‐Jin, Ki, Chang‐Seok, Kim, Seung Hyun

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MERS-CoV outbreak following a single patient exposure in an emergency room in South Korea: an epidemiological outbreak study von Cho, Sun Young, MD, Kang, Ji-Man, MD, Ha, Young Eun, MD, Park, Ga Eun, MD, Lee, Ji Yeon, MD, Ko, Jae-Hoon, MD, Lee, Ji Yong, MD, Kim, Jong Min, MD, Kang, Cheol-In, MD, Jo, Ik Joon, MD, Ryu, Jae Geum, RN, Choi, Jong Rim, RN, Kim, Seonwoo, PhD, Huh, Hee Jae, MD, Ki, Chang-Seok, Prof, Kang, Eun-Suk, Prof, Peck, Kyong Ran, Prof, Dhong, Hun-Jong, Prof, Song, Jae-Hoon, Prof, Chung, Doo Ryeon, Prof, Kim, Yae-Jean, Dr

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KCNJ3 is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing von Lee, Woong‐Woo, Lee, Cha Gon, Ki, Chang‐Seok

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Mutations in DDX58, which Encodes RIG-I, Cause Atypical Singleton-Merten Syndrome von Jang, Mi-Ae, Kim, Eun Kyoung, Now, Hesung, Nguyen, Nhung T.H., Kim, Woo-Jong, Yoo, Joo-Yeon, Lee, Jinhyuk, Jeong, Yun-Mi, Kim, Cheol-Hee, Kim, Ok-Hwa, Sohn, Seongsoo, Nam, Seong-Hyeuk, Hong, Yoojin, Lee, Yong Seok, Chang, Sung-A, Jang, Shin Yi, Kim, Jong-Won, Lee, Myung-Shik, Lim, So Young, Sung, Ki-Sun, Park, Ki-Tae, Kim, Byoung Joon, Lee, Joo-Heung, Kim, Duk-Kyung, Kee, Changwon, Ki, Chang-Seok

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Outcomes of Mycobacterium avium complex lung disease based on clinical phenotype von Koh, Won-Jung, Moon, Seong Mi, Kim, Su-Young, Woo, Min-Ah, Kim, Seonwoo, Jhun, Byung Woo, Park, Hye Yun, Jeon, Kyeongman, Huh, Hee Jae, Ki, Chang-Seok, Lee, Nam Yong, Chung, Myung Jin, Lee, Kyung Soo, Shin, Sung Jae, Daley, Charles L, Kim, Hojoong, Kwon, O Jung

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High prevalence of increased sitosterol levels in hypercholesterolemic children suggest underestimation of sitosterolemia incidence von Lee, Joon Hee, Song, Da Young, Jun, Sun-Hee, Song, Sang Hoon, Shin, Choong Ho, Ki, Chang-Seok, Lee, Kyunghoon, Song, Junghan

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Mycobacterial Characteristics and Treatment Outcomes in Mycobacterium abscessus Lung Disease von Koh, Won-Jung, Jeong, Byeong-Ho, Kim, Su-Young, Jeon, Kyeongman, Park, Kyoung Un, Jhun, Byung Woo, Lee, Hyun, Park, Hye Yun, Kim, Dae Hun, Huh, Hee Jae, Ki, Chang-Seok, Lee, Nam Yong, Kim, Hong Kwan, Choi, Yong Soo, Kim, Jhingook, Lee, Seung-Heon, Kim, Chang Ki, Shin, Sung Jae, Daley, Charles L., Kim, Hojoong, Kwon, O. Jung

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Carrier frequency and incidence estimation of Smith-Lemli-Opitz syndrome in East Asian populations by Genome Aggregation Database (gnomAD) based analysis von Park, Jong Eun, Lee, Taeheon, Ha, Kyeongsu, Ki, Chang-Seok

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Recent Advances in the Clinical Application of Next-Generation Sequencing von Ki, Chang-Seok

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Molecular classification of follicular thyroid carcinoma based on TERT promoter mutations von Park, Hyunju, Shin, Hyeong Chan, Yang, Heera, Heo, Jung, Ki, Chang-Seok, Kim, Hye Seung, Kim, Jung-Han, Hahn, Soo Yeon, Chung, Yun Jae, Kim, Sun Wook, Chung, Jae Hoon, Oh, Young Lyun, Kim, Tae Hyuk

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Age-associated mortality is partially mediated by TERT promoter mutation status in differentiated thyroid carcinoma von Heo, Jung, Lee, Sungjoo, Park, Jun, Yang, Heera, Park, Hyunju, Ki, Chang-Seok, Oh, Young Lyun, Kim, Hye In, Kim, Sun Wook, Chung, Jae Hoon, Kim, Kyunga, Kim, Tae Hyuk

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The first familial case of inherited intellectual developmental disorder with dysmorphic facies and behavioral abnormalities (IDDFBA) with a novel FBXO11 variant von Lee, Cha Gon, Seol, Chang Ahn, Ki, Chang‐Seok

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De novo mutations in SOD1 are a cause of ALS von Müller, Kathrin, Oh, Ki-Wook, Nordin, Angelica, Panthi, Sudhan, Kim, Seung Hyun, Nordin, Frida, Freischmidt, Axel, Ludolph, Albert C., Ki, Chang Seok, Forsberg, Karin, Weishaupt, Jochen, Kim, Young-Eun, Andersen, Peter Munch

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High-Resolution Magnetic Resonance Wall Imaging Findings of Moyamoya Disease von Ryoo, Sookyung, Cha, Jihoon, Kim, Suk Jae, Choi, Jin Wook, Ki, Chang-Seok, Kim, Keon Ha, Jeon, Pyoung, Kim, Jong-Soo, Hong, Seung-Chyul, Bang, Oh Young

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A nonsense variant in NME5 causes human primary ciliary dyskinesia with radial spoke defects von Cho, Eun Hye, Huh, Hee Jae, Jeong, Inyoung, Lee, Nam Yong, Koh, Won‐Jung, Park, Hae‐Chul, Ki, Chang‐Seok

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Carrier frequency and incidence estimation of RPE65-associated inherited retinal diseases in East Asian population by population database-based analysis von Cho, Eun Hye, Park, Jong Eun, Lee, Taeheon, Ha, Kyeongsu, Ki, Chang-Seok

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Intermittent antibiotic therapy for nodular bronchiectatic Mycobacterium avium complex lung disease von Jeong, Byeong-Ho, Jeon, Kyeongman, Park, Hye Yun, Kim, Su-Young, Lee, Kyung Soo, Huh, Hee Jae, Ki, Chang-Seok, Lee, Nam Yong, Shin, Sung Jae, Daley, Charles L, Koh, Won-Jung

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Long-term natural history of non-cavitary nodular bronchiectatic nontuberculous mycobacterial pulmonary disease von Moon, Seong Mi, Jhun, Byung Woo, Baek, Sun-Young, Kim, Seonwoo, Jeon, Kyeongman, Ko, Ryoung-Eun, Shin, Sun Hye, Lee, Hyun, Kwon, O Jung, Huh, Hee Jae, Ki, Chang-Seok, Lee, Nam Yong, Chung, Myung Jin, Lee, Kyung Soo, Shin, Sung Jae, Daley, Charles L., Koh, Won-Jung

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Molecular genotyping of the non‐invasive encapsulated follicular variant of papillary thyroid carcinoma von Kim, Tae Hyuk, Lee, Minju, Kwon, Ah‐Young, Choe, Jun‐Ho, Kim, Jung‐Han, Kim, Jee Soo, Hahn, Soo Yeon, Shin, Jung Hee, Chung, Man Ki, Son, Young Ik, Ki, Chang‐Seok, Yim, Hyun Sook, Kim, Yoo‐Li, Chung, Jae Hoon, Kim, Sun Wook, Oh, Young Lyun

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A Polymorphism in RNF213 Is a Susceptibility Gene for Intracranial Atherosclerosis von Bang, Oh Young, Chung, Jong-Won, Cha, Jihoon, Lee, Mi Ji, Yeon, Je Young, Ki, Chang-Seok, Jeon, Pyoung, Kim, Jong-Soo, Hong, Seung Chyul

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