http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
내용 쓰기(writing to learn)를 통한 영어 학습의 효과 및 이에 대한 학생들의 인식
나은정(Na, Eun Jeong),김태은(Kim, Tae-Eun) 한국외국어교육학회 2014 Foreign languages education Vol.21 No.3
This study investigates the effects of writing to learn on sixth graders’ English development compared with speaking to learn and examines their perceptions. The study established the following research questions: (a) what are the effects of writing to learn on English speaking and writing abilities compared with speaking to learn? and (b) what are the students’ perceptions of writing to learn compared with speaking to learn? Students in the experiment group had experienced learning English through writing to learn, whereas those in the comparison group had learned English through speaking to learn. As for the results, writing to learn had significant effects on developing speaking and writing abilities in terms of complexity, accuracy and fluency. Also the students had more positive perceptions on writing to learn in cognitive and behavioral perspectives. Writing to learn has been confirmed as effective in learning English, leading students to use English to express their own ideas with more extensive vocabulary and complicated syntactic structures.
영아 연축과 Lennox-Gastaut 증후군을 동반한 Miller-Dieker 증후군 1례
나정민(Jeong Min Na),박찬희(Chan Hee Park),유은정(Eun Jung Yoo),정권(Kwon Jung),김경심(Kyoung Sim Kim),김용욱(Yong Wook Kim),김은영(Eun Young Kim) 대한소아신경학회 2008 대한소아신경학회지 Vol.16 No.1
근간대성 경련을 주소로 내원한 11일된 여아로, 1형 활택뇌증과 특징적인 안면 이상, FISH에서 17p13.3의 미세 결실을 보여 Miller-Dieker 증후군으로 진단되었다. 경련은 4개월에 영아 연축, 3년 6개월에 Lennox-Gastaut 증후군으로 진행되었고, 항경련제에 의해 잘 조절되지 않았다. 현재 환아는 8세로, 심한 정신 운동 발달 지연과 심한 성장 부진을 보인다. 저자들은 난치성 간질을 동반하면서 장기간 생존해 있는 증례를 경험하였기에 문헌고찰과 함께 보고하며, 유전학의 최근 진전, 동반 간질, 유전상담을 중점적으로 기술하고자 하였다. Miller-Dieker syndrome is a contiguous gene deletion syndrome involving chromosome 17p13.3, which is characterized by type 1(classical) lissencephaly and typical craniofacial abnormalities. Children with Miller-Dieker syndrome have profound psychomotor retardation, seizures that often are intractable, chronic feeding problems that lead to recurrent pneumonia, and shortened lifespan. We have experienced a Miller-Dieker syndrome female who has lived to 8years, showing severe mental and motor retardation and intractable epilepsy. She was diagnosed as Miller-Dieker syndrome in the neonatal period, showing typical facial features, type 1 lissencephaly, and chromosome 17p13.3 microdeletion in fluorescence in situ hybridization. Infantile spasm occurred at 4 months of age and progressed to Lennox-Gastaut syndrome at 3 years and 6 months, both of which were not controlled by antiepileptic drugs.