Sidt2 regulates hepatocellular lipid metabolism through autophagy von Chen, Xueru, Gu, Xuefan, Zhang, Huiwen

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Successful newborn screening for Gaucher disease using fluorometric assay in China von Kang, Lulu, Zhan, Xia, Gu, Xuefan, Zhang, Huiwen

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X-ray induced photodynamic therapy (PDT) with a mitochondria-targeted liposome delivery system von Gu, Xuefan, Shen, Chao, Li, Hua, Goldys, Ewa M., Deng, Wei

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Newborn screening of maple syrup urine disease and the effect of early diagnosis von Chen, Ting, Lu, Deyun, Xu, Feng, Ji, Wenjun, Zhan, Xia, Gao, Xiaolan, Qiu, Wenjuan, Zhang, Huiwen, Liang, Lili, Gu, Xuefan, Han, Lianshu

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Late-onset cblC defect: clinical, biochemical and molecular analysis von Ding, Si, Ling, Shiying, Liang, Lili, Qiu, Wenjuan, Zhang, Huiwen, Chen, Ting, Zhan, Xia, Xu, Feng, Gu, Xuefan, Han, Lianshu

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Clinical, biochemical, and genetic analysis of 28 Chinese patients with holocarboxylase synthetase deficiency von Ling, Shiying, Qiu, Wenjuan, Zhang, Huiwen, Liang, Lili, Lu, Deyun, Chen, Ting, Zhan, Xia, Wang, Yu, Gu, Xuefan, Han, Lianshu

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Determination of 7-ketocholesterol in plasma by LC-MS for rapid diagnosis of acid SMase-deficient Niemann-Pick disease von Lin, Na, Zhang, Huiwen, Qiu, Wenjuan, Ye, Jun, Han, Lianshu, Wang, Yu, Gu, Xuefan

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Synthesis and Evaluation of Hydroxymethyl Tetramides as Flow Improvers for Crude Oil von Xuefan Gu, Xuefan Gu, Peng Wang, Peng Wang, Zhen Guo, Zhen Guo, Weichao Du, Weichao Du, Sanbao Dong, Sanbao Dong

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Gene expression profiles in the brain of phenylketonuria mouse model reversed by the low phenylalanine diet therapy von Hong, Sha, Zhu, Tianwen, Zheng, Simin, Zhan, Xia, Xu, Feng, Gu, Xuefan, Liang, Lili

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Characteristics of Pompe disease in China: a report from the Pompe registry von Zhao, Yuying, Wang, Zhaoxia, Lu, Jiahong, Gu, Xuefan, Huang, Yonglan, Qiu, Zhengqing, Wei, Yanping, Yan, Chuanzhu

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Screening of 1.17 million newborns for inborn errors of metabolism using tandem mass spectrometry in Shanghai, China: A 19-year report von Hao, Lili, Liang, Lili, Gao, Xiaolan, Zhan, Xia, Ji, Wenjun, Chen, Ting, Xu, Feng, Qiu, Wenjuan, Zhang, Huiwen, Gu, Xuefan, Han, Lianshu

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Synthesis of New Hydrazone Compounds from Natural Grease and Investigation as Flow Improver for Crude Oil von Zhang, Shu, Wang, Longyu, Cao, Pengzhang, Gu, Xuefan, Zhang, Huani, Chen, Gang

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SID1 transmembrane family, member 2 (Sidt2): A novel lysosomal membrane protein von Jialin, Gao, Xuefan, Gu, Huiwen, Zhang

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Novel PYGL mutations in Chinese children leading to glycogen storage disease type VI: two case reports von Luo, Xiaomei, Hu, Jiacheng, Gao, Xueren, Fan, Yanjie, Sun, Yu, Gu, Xuefan, Qiu, Wenjuan

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Diagnostic yield of additional exome sequencing after the detection of long continuous stretches of homozygosity (LCSH) in SNP arrays von Fan, Yanjie, Wang, Lili, Sun, Yu, Xu, Ting, Gong, Zhuwen, Zhao, Qianfeng, Qiu, Wenjuan, Liang, Lili, Xiao, Bing, Zhang, Huiwen, Han, Lianshu, Lin, Fujun, Xu, Rang, Gu, Xuefan, Yu, Yongguo

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Clinical and molecular characteristics of 69 Chinese patients with ornithine transcarbamylase deficiency von Lu, Deyun, Han, Feng, Qiu, Wenjuan, Zhang, Huiwen, Ye, Jun, Liang, Lili, Wang, Yu, Ji, Wenjun, Zhan, Xia, Gu, Xuefan, Han, Lianshu

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Demographic characteristics and distribution of lysosomal storage disorder subtypes in Eastern China von Chen, Xueru, Qiu, Wenjuan, Ye, Jun, Han, Lianshu, Gu, Xuefan, Zhang, Huiwen

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Next-generation sequencing analysis of twelve known causative genes in congenital hypothyroidism von Fan, Xin, Fu, Chunyun, Shen, Yiping, Li, Chuan, Luo, Shiyu, Li, Qifei, Luo, Jingsi, Su, Jiasun, Zhang, Shujie, Hu, Xuyun, Chen, Rongyu, Gu, Xuefan, Chen, Shaoke

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Performance and Mechanism of Span Surfactants as Clean Flow Improvers for Crude Oil von Xuefan Gu, Gao, Long, Li, Yongfei, Chen, Shijun, Zhang, Jie, Du, Weichao, Qu, Chengtun, Chen, Gang

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Three novel mutations of the FBN1 gene in Chinese children with acromelic dysplasia von Wang, Yu, Zhang, Huiwen, Ye, Jun, Han, Lianshu, Gu, Xuefan

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