Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mei-Chyn Chao"'
Autor:
Dau Ming Niu, Huei Ching Chiu, Mei Chyn Chao, Ni-Chung Lee, Fuu Jen Tsai, Ru Yi Tu, Shuan-Pei Lin, Hsiang-Yu Lin, Yin-Hsiu Chien, Yen Yin Chou, You Hsin Huang, Chih-Kuang Chuang, Chung Lin Lee, Li Ping Tsai
Publikováno v:
American journal of medical genetics. Part A. 176(6)
Prader-Willi syndrome (PWS) is a genetic disorder with obesity, developmental delay, short stature, and behavioral abnormalities. The study aimed to assess the functional independence in children with PWS. The Functional Independence Measure for Chil
Autor:
Cheng Hung Huang, Pao Lin Kuo, Ming-Ren Chen, Mei-Chyn Chao, Jui-Lung Yen, Hsiang-Yu Lin, Li-Ping Tsai, Chi-Yu Huang, I-Ching Chou, Ju-Li Lin, Shuan-Pei Lin, Fuu Jen Tsai, Chih-Kuang Chuang, Pao-Ching Chiu
Publikováno v:
Journal of the Chinese Medical Association, Vol 71, Iss 6, Pp 305-309 (2008)
BackgroundInformation regarding the efficacy of growth hormone (GH) therapy in Asian Prader-Willi syndrome (PWS) patients is lacking. We report our experience with GH treatment in children with PWS in Taiwan.MethodsForty-six PWS patients (27 males, 1
Autor:
Li-Ping Tsai, Nan-Chang Chiu, Dau-Ming Niu, Che-Sheng Ho, Pao Lin Kuo, Jui-Lung Yen, Shuan-Pei Lin, Han-Yang Hung, Mei-Chyn Chao, Jui-Hsing Chang, Chi-Yu Huang, Hsiang-Yu Lin, Chyong-Hsin Hsu, Yann-Jinn Lee, Hsin-An Kao
Publikováno v:
Pediatrics International. 49:375-379
Background: Prader–Willi syndrome (PWS) is a congenital disorder caused by absent expression of paternal genes in 15q11-13 affecting multiple systems. The information concerning the clinical features of this genetic disorder is incomplete in Taiwan
Autor:
Hsiang-Yu, Lin, Shuan-Pei, Lin, Chih-Kuang, Chuang, Ming-Ren, Chen, Jui-Lung, Yen, Yann-Jinn, Lee, Chi-Yu, Huang, Li-Ping, Tsai, Dau-Ming, Niu, Mei-Chyn, Chao, Pao-Lin, Kuo
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 96(6)
Several different genetic defects have been found to result in the characteristic phenotypic expression of Prader-Willi syndrome (PWS).We performed a retrospective analysis of 67 cases of molecularly confirmed PWS diagnosed from January 1980 through