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Journal of Human Genetics|December 24, 2005
Mutation analysis of the GNE gene in Korean patients with distal myopathy with rimmed vacuolesByoung Joon Kim, Chang-Seok Ki, Jong-Won Kim, et al.
Sensors (Basel, Switzerland)|July 2, 2021
Patch-Type Vibration Visualization (PVV) Sensor System Based on Triboelectric EffectSun-Jin Kim, Myeong-Lok Seol, Byun-Young Chung, et al.
Journal of Human Genetics|February 9, 2020
Erratum to: Mutation analysis of the GNE gene in Korean patients with distal myopathy with rimmed vacuolesByoung Joon Kim, Chang-Seok Ki, Jong-Won Kim, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|August 24, 2019
Proteomic analysis of the skeletal muscles from dysferlinopathy patientsYoung-Chul Choi, Ji-Man Hong, Kee Duk Park, et al.
Yonsei Medical Journal|March 9, 2004
A case of congenital neuromuscular disease with uniform type 1 fiberSang-Jun Na, Seong-Woong Kang, Kee-Oog Lee, et al.
Journal of Clinical Neurology (Seoul, Korea)|January 16, 2010
Clinical Diversity of SCN4A-Mutation-Associated Skeletal Muscle Sodium ChannelopathySang-Chan Lee, Hyang-Sook Kim, Yeong-Eun Park, et al.
Yonsei Medical Journal|August 28, 2007
A case of adult polyglucosan body diseaseSeung-Yeob Lee, Jae-Hyeon Park, So Hun Kim, et al.
Neuromuscular Disorders : NMD|February 3, 2012
Two common mutations (p.Gln832X and c.663+1G>C) account for about a third of the DYSF mutations in Korean patients with dysferlinopathyYoung-Eun Park, Hyang-Sook Kim, Chang-Hoon Lee, et al.
Journal of Korean Medical Science|June 18, 2004
Clinical and pathological characteristics of four Korean patients with limb-girdle muscular dystrophy type 2BSeung-Hun Oh, Seong-Woong Kang, Jin-Goo Lee, et al.
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