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Journal of the Neurological Sciences|December 17, 2017
Clinical and genetic diversity of nemaline myopathy from a single neuromuscular center in KoreaJong-Mok Lee, Jeong Geun Lim, Jin-Hong Shin, et al.
Journal of the Neurological Sciences|March 22, 2017
RNF213 rs112735431 polymorphism in intracranial artery steno-occlusive disease and moyamoya disease in KoreansMin-Gyu Park, Jin-Hong Shin, Sang Weon Lee, et al.
Molecular Therapy. Methods & Clinical Development|June 25, 2020
rAAV8 and rAAV9-Mediated Long-Term Muscle Transduction with Tacrolimus (FK506) in Non-Human PrimatesAkiko Ishii, Hironori Okada, Hiromi Hayashita-Kinoh, et al.
The Korean Journal of Physiology & Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology|July 15, 2017
Electrophysiological characteristics of R47W and A298T mutations in CLC-1 of myotonia congenita patients and evaluation of clinical featuresHyung Jin Chin, Chan Hyeong Kim, Kotdaji Ha, et al.
Human Gene Therapy|December 14, 2022
Lifelong Outcomes of Systemic Adeno-Associated Virus Micro-Dystrophin Gene Therapy in a Murine Duchenne Muscular Dystrophy ModelNalinda B Wasala, Yongping Yue, Bryan Hu, et al.
Plos One|September 14, 2012
Dystrophin deficiency compromises force production of the extensor carpi ulnaris muscle in the canine model of Duchenne muscular dystrophyHsiao T Yang, Jin-Hong Shin, Chady H Hakim, et al.
European Journal of Gastroenterology & Hepatology|January 7, 2016
NUDT15 variant is the most common variant associated with thiopurine-induced early leukopenia and alopecia in Korean pediatric patients with Crohn's diseaseYeoun Joo Lee, Eun Ha Hwang, Jae Hong Park, et al.
IEEE Transactions on Neural Systems and Rehabilitation Engineering : a Publication of the IEEE Engineering in Medicine and Biology Society|April 7, 2023
Digital Biomarkers for Diagnosis of Muscle Disorders Using Stimulated Muscle Contraction SignalKwangsub Song, Sangui Choi, Jin-Hong Shin, et al.
Plos One|February 12, 2014
Characterization of 65 epitope-specific dystrophin monoclonal antibodies in canine and murine models of duchenne muscular dystrophy by immunostaining and western blotKasun Kodippili, Lauren Vince, Jin-Hong Shin, et al.
Neurocase|February 21, 2023
Clinical, electrophysiological, and genetic characteristics of cerebrotendinous xanthomatosis in South KoreaSunyoung Kim, Jin-Sung Park, Jae-Hyeok Lee, et al.
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