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가족 캠핑활동 참여자의 전문화 수준에 따른 장소 애착과 지각된 가치 : 레크리에이션 전문화 척도 비교
정하늘,류성옥 한국사회체육학회 2019 한국사회체육학회지 Vol.0 No.75
Purpose: Previous empirical studies have paid less attention to the slfe-classification measure for assessing respondents’ levels of recreation specialization since the multi-dimensional scale has been believed to more effectively encompass the three elements of specialization. The main purpose of this paper is to test the measurement effectiveness of recreation specialization by comparing the two scales. Using the context of South Korean campers, this study also aims to better understand how campers’ place attachment and perceived values are varied according to their levels of camping specialization. Method: The online interviewee of 692 people who went camping last year were chosen as subjects of the study. Results: The results of this study suggested that place identity and edpendence, the two domains of place attachment, increase as respondents’ levels of specialization increase. They also indicated a positive conceptual relationship between recreation specialization and perceived values. Most importantly, a series of tests fail to revealed significant differences between the two recreation specialization measures. Conclusion: Based on the study results, this paper suggests several usefl umarketing strategies to maximize camper’s satisfaction.
Clinical and Pathologic Findings of Korean Patients with RYR1-Related Congenital Myopathy
정하늘,박형준,이정환,신하영,김세훈,김승민,최영철 대한신경과학회 2018 Journal of Clinical Neurology Vol.14 No.1
Background and Purpose This study was designed to investigate clinical and pathologic characteristics of five Korean patients with RYR1-related congenital myopathy (CM). Methods Five patients from unrelated families were diagnosed with RYR1-related CM via direct or targeted sequencing of RYR1. Their clinical, mutational, and pathologic findings were then analyzed. Results Seven different mutations were identified, including two novel mutations: c.5915A> T and c.12250C>T. All of the patients presented at infancy with proximal dominant weakness and delayed motor milestones. Other clinical findings were scoliosis in three patients, winged scapula in two, hip dislocation in one, and pectus excavatum in one. Ophthalmoplegia was observed in one patient with a novel recessive mutation. Two of three muscle specimens revealed a myopathic pattern with core. Conclusions We have identified a novel compound heterozygous RYR1 mutation and demonstrated clinical and pathologic findings in five Korean patients with RYR1-related CM.