Suchergebnisse - Hong-ping Yu

Determination of the median effective dose of sufentanil for inhibiting the laryngeal mask insertion response in geriatric patients: a prospective, double-blinded, dose–response tr... von ShiFang Wang, WeiBing Wang, JinBo Xiao, HongPing Yu, Hui Zhou, Huang Xu

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Case report: a rare concurrence of dense deposit disease in an adolescent patient with IgA nephropathy von Jian-Hui Zhang, Hong-Ping Yu, Ying Chen, Qian Chen, Xiao-Ling Zheng, Jie-Wei Luo, Li Zhang

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Analyzing three pedigrees in X-linked Alport syndrome with the presentation of nephrotic syndrome von Jian-Hui Zhang, Jian-Hui Zhang, Jie Liu, Jie Liu, Dan-Dan Ruan, Dan-Dan Ruan, Qian Chen, Qian Chen, Jie Yang, Jie Yang, Min Wu, Min Wu, Hong-Ping Yu, Hong-Ping Yu, Li-Sheng Liao, Li-Sheng Liao, Xiao-Ling Zheng, Xiao-Ling Zheng, Jie-Wei Luo, Li Zhang, Li Zhang

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A rare concurrence of acute tubular necrosis and chronic glomerular sclerosis in a patient with wasp stings von Jian-hui Zhang, Jing Zou, Dan-dan Ruan, Qian Chen, Min Wu, Hong-ping Yu, Qiu-yan Wu, Fan Lin, Jie-wei Luo, Li Zhang

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A novel splicing mutation DNAH5 c.13,338 + 5G > C is involved in the pathogenesis of primary ciliary dyskinesia in a family with primary familial brain calcification von Xiu-juan Yao, Qian Chen, Hong-ping Yu, Dan-dan Ruan, Shi-jie Li, Min Wu, Li-sheng Liao, Xin-fu Lin, Zhu-ting Fang, Jie-wei Luo, Bao-song Xie

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Association between polymorphisms in MicroRNA target sites of RAD51D genes and risk of hepatocellular carcinoma von Yan‐Ji Jiang, Jian‐Hong Zhong, Zi‐Han Zhou, Mo‐Qin Qiu, Xian‐Guo Zhou, Ying‐Chun Liu, Rong‐Rui Huo, Xiu‐Mei Liang, Zhu Chen, Qiu‐Ling Lin, Xiang‐Yuan Yu, Hong‐Ping Yu

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Diagnostic journey and genetic analysis of a novel homozygous CYP2U1 mutation causing autosomal recessive spastic paraplegia type 56 (SPG56) in a consanguineous family von Hong-ping Yu, Jing Zou, Xiang Chen, Ying Chen, Dan-dan Ruan, Qian Chen, Jian-hui Zhang, Qiong Cheng, Xing-lin Ruan, Wei Wen, Li Chen, Jie-wei Luo, Yun-fei Li, Xiao-lin Jiang

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Genetic analysis of a novel TSC1 splice mutation causing tuberous sclerosis without neurological phenotypes von Xiu-juan Yao, Ying Lin, Jing Zou, Zun-lin Cai, Zi-Yan Xu, Xiao-qin Li, Qian Chen, Hong-ping Yu, Jian-hui Zhang, Dan-dan Ruan, Mei-zhu Gao, Li Zhang, Jie-wei Luo, Bao-song Xie

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Clinical genetic analysis of an adult polyglucosan body disease (APBD) family caused by the compound heterozygous variant of GBE1 p.R156C and deletion exon 3-7 von Juan Zhu, Hong-Ping Yu, Jing Zou, Yi-Wu Zhang, Xin-Qi Han, Zi-Yan Xu, Li Chen, Qian Chen, Mei-Zhu Gao, Li-Jun Xie, Xi-Kui Zhang, Jie-Wei Luo, Yun-Fei Li, Yun-Fei Li, Li Zhang

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A novel NOTCH1 nonsense variant in a bicuspid aortic valve family with intrafamilial clinical heterogeneity von Qian Chen, Zi-yan Xu, Wu Chi, Xiang Chen, Jing Zou, Ting Chen, Meng-qian Wu, Dan-dan Ruan, Hong-ping Yu, Jian-hui Zhang, Mei-zhu Gao, Li Zhang, Li-sheng Liao, Zhu-ting Fang, Fan Lin, Jie-wei Luo, Li Chen

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Radiotherapy plus anti-PD1 versus radiotherapy for hepatic toxicity in patients with hepatocellular carcinoma von Rui-Jun Zhang, Hong-Mei Zhou, Hai-Yan Lu, Hong-Ping Yu, Wei-Zhong Tang, Mo-Qin Qiu, Liu-Ying Yan, Mei-Ying Long, Ting-Shi Su, Bang-De Xiang, Mei-Ling He, Xiao-Ting Wang, Shi-Xiong Liang, Jian-Xu Li

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In vitro study of ATP1A3 p.Ala275Pro mutant causing alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism von Dan-dan Ruan, Jing Zou, Li-sheng Liao, Li-sheng Liao, Ming-dong Ji, Ruo-li Wang, Ruo-li Wang, Jian-hui Zhang, Li Zhang, Li Zhang, Mei-zhu Gao, Mei-zhu Gao, Qian Chen, Hong-ping Yu, Wen Wei, Yun-fei Li, Yun-fei Li, Hong Li, Fan Lin, Fan Lin, Jie-wei Luo, Xin-fu Lin, Xin-fu Lin

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