Search Results - Luo, Jie-wei

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  1. 1
    Genetic analysis of sick sinus syndrome in a family harboring compound CACNA1C and TTN mutations

    Genetic analysis of sick sinus syndrome in a family harboring compound CACNA1C and TTN mutations by Zhu, Yao-Bin, Luo, Jie-Wei, Jiang, Fen, Liu, Gui

    Published 2018
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  2. 2
    N,N′-Bis(4-nitro­phen­yl)biphenyl-2,2′-dicarboxamide

    N,N′-Bis(4-nitro­phen­yl)biphenyl-2,2′-dicarboxamide by Wang, Gui-Yu, Qin, Da-Bin, Guo, Li-Hui, Luo, Jie-Wei

    Published 2010
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  3. 3
    Bis(3-bromo­methyl-2-meth­oxy-1-naphth­yl)methane

    Bis(3-bromo­methyl-2-meth­oxy-1-naphth­yl)methane by Luo, Jie-Wei, Zhou, Li, He, Rui, Wang, Gui-Yu, Qin, Da-Bin

    Published 2008
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  4. 4
    N,N′-Bis(2-methoxy­phen­yl)biphenyl-2,2′-dicarboxamide

    N,N′-Bis(2-methoxy­phen­yl)biphenyl-2,2′-dicarboxamide by Wang, Gui-Yu, Li, Di, Qin, Da-Bin, Luo, Jie-Wei, Guo, Li-Hui

    Published 2008
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  5. 5
    9,10-Bis{2-[1-(2-pyridylmeth­yl)imidazolium-3-yl]eth­oxy}anthracene bis(hexa­fluoridophosphate)

    9,10-Bis{2-[1-(2-pyridylmeth­yl)imidazolium-3-yl]eth­oxy}anthracene bis(hexa­fluoridophosphate) by Guo, Li-Hui, Qin, Da-Bin, Gu, Shao-Jin, Wang, Gui-Yu, Luo, Jie-Wei

    Published 2007
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  6. 6
    Genetic mutation of familial dilated cardiomyopathy based on next-generation semiconductor sequencing

    Genetic mutation of familial dilated cardiomyopathy based on next-generation semiconductor sequencing by Lin, Xin-Fu, Luo, Jie-Wei, Liu, Gui, Zhu, Yao-Bin, Jin, Zhao, Lin, Xing

    Published 2018
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  7. 7
    Association of Tongue Bacterial Flora and Subtypes of Liver-Fire Hyperactivity Syndrome in Hypertensive Patients

    Association of Tongue Bacterial Flora and Subtypes of Liver-Fire Hyperactivity Syndrome in Hypertensive Patients by Luo, Jie-wei, Lin, Cong-huai, Zhu, Yao-bin, Zheng, Xing-yu, Wu, Yong-xi, Chen, Wei-wei, Yang, Xiao

    Published 2018
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  8. 8
    Screening and function discussion of a hereditary renal tubular acidosis family pathogenic gene

    Screening and function discussion of a hereditary renal tubular acidosis family pathogenic gene by Chen, Li, Wang, Han-Lu, Zhu, Yao-Bin, Jin, Zhao, Huang, Jian-Bin, Lin, Xin-Fu, Luo, Jie-Wei, Fang, Zhu-Ting

    Published 2020
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  9. 9
    Splenic Artery Embolization and Splenectomy for Spontaneous Rupture of Splenic Hemangioma and Its Imaging Features

    Splenic Artery Embolization and Splenectomy for Spontaneous Rupture of Splenic Hemangioma and Its Imaging Features by Lin, Jia-Li, Lin, Can, Wang, Han-Lu, Wu, Shao-Jie, Tang, Yi, Yang, Chang Shun, Luo, Jie-Wei, Chi, Wu, Fang, Zhu-Ting

    Published 2022
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  10. 10
    Mutational Analysis of a Familial Adenomatous Polyposis Pedigree with Bile Duct Polyp Phenotype

    Mutational Analysis of a Familial Adenomatous Polyposis Pedigree with Bile Duct Polyp Phenotype by Xie, Li-jun, Ruan, Dan-dan, Zhang, Jian-hui, Li, Yi, Chen, Li, Yan, Mao-lin, Yu, Ming-dian, Luo, Jie-wei, Zhang, Hui-zhen

    Published 2021
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  11. 11
    A Primary Extraskeletal Osteosarcoma of the Spleen: Rare Case Report

    A Primary Extraskeletal Osteosarcoma of the Spleen: Rare Case Report by Pan, Xian, Wang, Han-Lu, Lin, Shi-Ming, Lin, Jia-Li, Ruan, Dan-Dan, Zhang, Jian-Hui, Chen, Ting, Luo, Jie-Wei, Fang, Zhu-Ting

    Published 2022
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  12. 12
    Differences in gut microbiota structure in patients with stages 4-5 chronic kidney disease

    Differences in gut microbiota structure in patients with stages 4-5 chronic kidney disease by Wu, Rong, Ruan, Xing-Lin, Ruan, Dan-Dan, Zhang, Jian-Hui, Wang, Han-Lu, Zeng, Quan-Zuan, Lu, Tao, Gan, Yu-Mian, Luo, Jie-Wei, Wu, Jia-Bin

    Published 2021
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  13. 13
    The Construction of Unsmooth Pulse Images in Traditional Chinese Medicine Based on Wave Intensity Technology

    The Construction of Unsmooth Pulse Images in Traditional Chinese Medicine Based on Wave Intensity Technology by Luo, Jie-wei, Guo, Si-wei, Cao, Shuang-shuang, Lin, Ning, Ye, Zhen-sheng, Wei, Shi-chao, Zheng, Xing-yu, Guo, Miao-miao, Meng, Xiao-rong, Huang, Fang-meng

    Published 2016
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  14. 14
    Genetic diagnosis history and osteoarticular phenotype of a non-transfusion secondary hemochromatosis

    Genetic diagnosis history and osteoarticular phenotype of a non-transfusion secondary hemochromatosis by Ruan, Dan-Dan, Gan, Yu-Mian, Lu, Tao, Yang, Xiao, Zhu, Yao-Bin, Yu, Qing-Hua, Liao, Li-Sheng, Lin, Ning, Qian, Xin, Luo, Jie-Wei, Tang, Fa-Qiang

    Published 2020
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  15. 15
    Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations

    Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations by Zhang, Jian-hui, Ruan, Dan-dan, Hu, Ya-nan, Ruan, Xing-lin, Zhu, Yao-bin, Yang, Xiao, Wu, Jia-bin, Lin, Xin-fu, Luo, Jie-wei, Tang, Fa-qiang

    Published 2021
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  16. 16
    Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A

    Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A by Zhu, Yao-Bin, Zhang, Jian-Hui, Ji, Yuan-Yuan, Hu, Ya-Nan, Wang, Han-Lu, Ruan, Dan-Dan, Meng, Xiao-Rong, Lin, Xin-Fu, Luo, Jie-Wei, Chen, Wei

    Published 2022
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  17. 17
    Clinical and Genetic Analysis of a Family With Sitosterolemia Caused by a Novel ATP-Binding Cassette Subfamily G Member 5 Compound Heterozygous Mutation

    Clinical and Genetic Analysis of a Family With Sitosterolemia Caused by a Novel ATP-Binding Cassette Subfamily G Member 5 Compound Heterozygous Mutation by Shen, Ming-fang, Hu, Ya-nan, Chen, Wei-xiang, Liao, Li-sheng, Wu, Min, Wu, Qiu-yan, Zhang, Jian-hui, Zhang, Yan-ping, Luo, Jie-wei, Lin, Xin-fu

    Published 2022
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  18. 18
    Retrospective Analysis of the Effect of Lidocaine Combined with Methylprednisolone on Pain Control After Uterine Artery Embolization

    Retrospective Analysis of the Effect of Lidocaine Combined with Methylprednisolone on Pain Control After Uterine Artery Embolization by Tang, Yi, Lin, Bin, Zhang, Yan-ping, Hu, Ya-nan, Zhang, Jian-hui, Wu, Shao-jie, Zhou, Yan-feng, Cai, Sen-lin, Luo, Jie-wei, Chi, Wu, Fang, Zhu-ting

    Published 2022
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  19. 19
    Genetic Analysis and Functional Study of a Pedigree With Bruck Syndrome Caused by PLOD2 Variant

    Genetic Analysis and Functional Study of a Pedigree With Bruck Syndrome Caused by PLOD2 Variant by Wang, Ruo-li, Ruan, Dan-dan, Hu, Ya-nan, Gan, Yu-mian, Lin, Xin-fu, Fang, Zhu-ting, Liao, Li-sheng, Tang, Fa-qiang, He, Wu-bing, Luo, Jie-wei

    Published 2022
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  20. 20
    Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription

    Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription by Gan, Yu-mian, Zhang, Yan-ping, Ruan, Dan-dan, Huang, Jian-bin, Zhu, Yao-bin, Lin, Xin-fu, Xiao, Xiao-ping, Cheng, Qiong, Geng, Zhen-bo, Liao, Li-sheng, Tang, Fa-qiang, Luo, Jie-wei

    Published 2022
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