Search Results - Ning Su

Current Aspects in the Molecular Genetics and Diagnostics of Spinal Muscular Atrophy by Shu-Chin Chien, Yi-Ning Su

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PHOX2B Mutation in a Taiwanese Newborn with Congenital Central Hypoventilation Syndrome by Tzu-Chiang Wang, Yi-Ning Su, Ming-Chi Lai

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Lethal fetal stroke in utero by Tzu-Hung Lin, Chien-Nan Lee, Yi-Ning Su

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A blended face-to-face and eHealth lifestyle intervention on physical activity, diet, and health outcomes in Hong Kong community-dwelling older adults: a study protocol for a rando... by Min Yang, Yanping Duan, Sonia Lippke, Wei Liang, Ning Su

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Pelizaeus-Merzbacher Disease, Easily Misdiagnosed as Cerebral Palsy: A Report of a Three-generation Family by Yen-Chun Chen, Wen-Chen Liang, Yi-Ning Su, Yuh-Jyh Jong

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Effects of dietary intake of Colla corii asini on skin parameters and appearance: Results of a 12-week randomized, controlled, open-labeled trial by Yumei Fan, Wenwen Ru, Ning Su, Hongyan Zheng, Juan Liu, Haiqing Zhao, Feng Liao

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Prenatal diagnosis of microvillus inclusion disease by Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Pei-Chen Wu, Wayseen Wang

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Septic Shock after Intracervical Laminaria Insertion by Shin-Yu Lin, Wen-Fang Cheng, Yi-Ning Su, Chi-An Chen, Chien-Nan Lee

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Split hand/foot malformations with microdeletions at chromosomes 7 and 19 detected using array comparative genomic hybridization by Chin-Jui Wu, Yi-Ning Su, Tzu-Hung Lin, Li-Hui Tseng, Kuang-Han Chao

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Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus ass... by Ya-Lien Hsueh, Yi-Ning Su, Hsin-Yu Lin, Chien-Nan Lee, Jin-Chung Shih

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Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: Prenatal diagnosis and literature review by Chih-Ping Chen, Yi-Ning Su, Tzu-Hung Lin, Tung-Yao Chang, Jun-Wei Su, Wayseen Wang

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Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism by Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

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Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome by Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

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Identification of a deletion mutation in the short flanking repeat region of exon 44 of the COL1A1 gene in a fetus with osteogenesis imperfecta type II by Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

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Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene by Chih-Ping Chen, Yi-Ning Su, Yu-Ting Chen, Wen-Lin Chen, Lee James Hsu, Wayseen Wang

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Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II by Chih-Ping Chen, Yi-Ning Su, Fang-Yu Hung, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

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Prenatal diagnosis of proximal femoral focal deficiency: A case report and literature review by Tzu-Hung Lin, Chi-Hsien Chung, Jin-Chung Shih, Chia-Hui Lin, Chien-Nan Lee, Yi-Ning Su

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Intraperitoneal and intracardiac transfusion of recurrent fetal erythroblastosis due to anti-M alloimmunization with unfavorable outcome by Tzu-Hung Lin, Jin-Chung Shih, Chia-Hui Lin, Shin-Yu Lin, Yi-Ning Su, Chien-Nan Lee

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Manifesting Pediatric Carrier of Isolated Dystrophinopathy with Initial Presentation of Myalgia and Persistent HyperCKemia by Chien-Hua Wang, Wen-Chen Liang, Yi-Ning Su, Wen-Chieh Lee, Ching-Chyuan Su, Yuh-Jyh Jong

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Electronic Health Literacy Scale-Web3.0 for Older Adults with Noncommunicable Diseases: Validation Study by Wenfei Cai, Wei Liang, Huaxuan Liu, Rundong Zhou, Jie Zhang, Lin Zhou, Ning Su, Hanxiao Zhu, Yide Yang

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