A Metaheuristic Hybrid of Double-Target Multi-Layer Perceptron for Energy Performance Analysis in Residential Buildings von Lin, Cheng, Lin, Yunting

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Comparative Effects of Exosomes and Ectosomes Isolated From Adipose-Derived Mesenchymal Stem Cells on Achilles Tendinopathy in a Rat Model von Xu, Tengjing, Lin, Yunting, Yu, Xinning, Jiang, Guangyao, Wang, Jiajie, Xu, Kaiwang, Fang, Jinghua, Wang, Siheng, Dai, Xuesong

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Reproductive hormones and sex differences in relation to brachial-ankle pulse wave velocity in obese subjects: a retrospective case-control study von Lin, Yunting, Song, Endi, Jin, Han, Jin, Yong

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Two De Novo Mosaic Variants Within the Same Site of PHEX Gene in a Girl with X-Linked Hypophosphatemic Rickets von Lin, Yunting, Zhang, Wen, Huang, Xinjiang, Su, Ling, Cai, Yanna, Liang, Cuili, Rao, Min, Liu, Li, Zeng, Chunhua

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UBA5 Mutations Cause a New Form of Autosomal Recessive Cerebellar Ataxia von Duan, Ranhui, Shi, Yuting, Yu, Li, Zhang, Gehan, Li, Jia, Lin, Yunting, Guo, Jifeng, Wang, Junling, Shen, Lu, Jiang, Hong, Wang, Guanghui, Tang, Beisha

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Clinical and genetic analysis of methylmalonic aciduria in 60 patients from Southern China: a single center retrospective study von Su, Ling, Sheng, Huiying, Li, Xiuzhen, Cai, Yanna, Mei, Huifen, Cheng, Jing, Li, Duan, Lu, Zhikun, Lin, Yunting, Chen, Xiaodan, Peng, Minzhi, Huang, Yonglan, Zhang, Wen, Liu, Li

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Natural history and outcome of nonketotic hyperglycinemia in China von Zhou, Zhizi, Cai, Yanna, Li, Xiuzhen, Liu, Zongcai, Peng, Minzhi, Lin, Yunting, Mao, Xiaojian, Zeng, Chunhua, Liu, Li, Zhang, Wen

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Neddylation activity modulates the neurodegeneration associated with fragile X associated tremor/ataxia syndrome (FXTAS) through regulating Sima von Lin, Yunting, Xue, Jin, Deng, Jing, He, Hua, Luo, Shiyu, Chen, Jia, Li, Jia, Yu, Li, Zhao, Juan, Chen, Jing, Allen, Emily G., Jin, Peng, Duan, Ranhui

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Comparison of the ability of exosomes and ectosomes derived from adipose-derived stromal cells to promote cartilage regeneration in a rat osteochondral defect model von Xu, Tengjing, Yu, Xinning, Xu, Kaiwang, Lin, Yunting, Wang, Jiajie, Pan, Zongyou, Fang, Jinghua, Wang, Siheng, Zhou, Zhuxing, Song, Hongyun, Zhu, Sunan, Dai, Xuesong

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Assessment of the diagnostic value of serum ceruloplasmin for Wilson's disease in children von Lu, Xinshuo, Li, Simin, Zhang, Wen, Lin, Yunting, Lu, Zhikun, Cai, Yanna, Su, Xueying, Shao, Yongxian, Liu, Zongcai, Sheng, Huiying, Huang, Yonglan, Liu, Li, Zeng, Chunhua

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Activation of mTOR ameliorates fragile X premutation rCGG repeat-mediated neurodegeneration von Lin, Yunting, Tang, Chengyuan, He, Hua, Duan, Ranhui

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Amyotrophic Lateral Sclerosis-associated GGGGCC repeat expansion promotes Tau phosphorylation and toxicity von He, Hua, Huang, Wen, Wang, Ruoxi, Lin, Yunting, Guo, Yichen, Deng, Jing, Deng, Haitao, Zhu, Yanping, Allen, Emily G., Jin, Peng, Duan, Ranhui

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Novel variants and phenotypic heterogeneity in a cohort of 11 Chinese children with Wiedemann-Steiner syndrome von Lin, Yunting, Chen, Xiaohong, Xie, Bobo, Guan, Zhihong, Chen, Xiaodan, Li, Xiuzhen, Yi, Peng, Du, Rong, Mei, Huifen, Liu, Li, Zhang, Wen, Zeng, Chunhua

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Features of chinese patients with sitosterolemia von Zhou, Zhizi, Su, Xueying, Cai, Yanna, Ting, Tzer Hwu, Zhang, Wen, Lin, Yunting, Xu, Aijing, Mao, Xiaojian, Zeng, Chunhua, Liu, Li, Li, Xiuzhen

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Clinical Management and Gene Mutation Analysis of Children with Congenital Hyperinsulinism in South China von Xu, Aijing, Cheng, Jing, Sheng, Huiying, Wen, Zhe, Lin, Yunting, Zhou, Zhihong, Zeng, Chunhua, Shao, Yongxian, Li, Cuiling, Liu, Li, Li, Xiuzhen

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Chinese family with Blau syndrome: Mutated NOD2 allele transmitted from the father with de novo somatic and germ line mosaicism von Lin, Yunting, Zeng, Chunhua, Chen, Xiaodan, Li, Taolin, Liu, Huazhen, Liu, Hongsheng, Hu, Hao, Liu, Li

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Genetic and clinical characteristics of Chinese children with Glucokinase-maturity-onset diabetes of the young (GCK-MODY) von Li, Xiuzhen, Ting, Tzer Hwu, Sheng, Huiying, Liang, Cui Li, Shao, Yongxian, Jiang, Minyan, Xu, Aijing, Lin, Yunting, Liu, Li

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Two novel mutations in the ALPL gene of unrelated Chinese children with Hypophosphatasia: case reports and literature review von Mao, Xiaojian, Liu, Sichi, Lin, Yunting, Chen, Zhen, Shao, Yongxian, Yu, Qiaoli, Liu, Haiying, Lu, Zhikun, Sheng, Huiyin, Lu, Xinshuo, Huang, Yonglan, Liu, Li, Zeng, Chunhua

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Distinct severity of phenotype in Hajdu-Cheney syndrome: a case report and literature review von Zeng, Chunhua, Lin, Yunting, Lu, Zhikun, Chen, Zhen, Jiang, Xiaoling, Mao, Xiaojian, Liu, Zongcai, Lu, Xinshuo, Zhang, Kangdi, Yu, Qiaoli, Wang, Xiaoya, Huang, Yonglan, Liu, Li

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Glucose-6-Phosphate dehydrogenase deficiency associated hemolysis in a cohort of new onset type 1 diabetes children in Guangdong province, China von Xu, Aijing, Jiang, Minyan, Zhang, Wen, Lin, Yunting, Shao, Yongxian, Mei, Huifen, Cheng, Jing, Liang, Cuili, Li, Cuiling, Li, Xiuzhen, Liu, Li

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