A natural history comparison of SOD1-mutant patients with amyotrophic lateral sclerosis between Chinese and German populations

被引:11
|
作者
Tang, Lu [1 ,2 ]
Dorst, Johannes [3 ,4 ]
Chen, Lu [1 ,2 ]
Liu, Xiaolu [1 ,2 ]
Ma, Yan [1 ,2 ]
Guenther, Kornelia [3 ]
Michels, Sebastian [3 ]
Mueller, Kathrin [3 ]
Freischmidt, Axel [3 ]
Weishaupt, Jochen H. [3 ]
Fan, Dongsheng [1 ,2 ]
Ludolph, Albert C. [3 ,4 ]
机构
[1] Peking Univ Third Hosp, Dept Neurol, Beijing 100191, Peoples R China
[2] Peking Univ Third Hosp, Beijing Key Lab Biomarker & Translat Res Neurodeg, Beijing 100191, Peoples R China
[3] Ulm Univ, Dept Neurol, D-89081 Ulm, Germany
[4] German Ctr Neurodegenerat Dis DZNE, Ulm Site, D-89081 Ulm, Germany
基金
中国国家自然科学基金;
关键词
TRIAL;
D O I
10.1186/s40035-021-00266-x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
引用
收藏
页数:3
相关论文
共 50 条
  • [1] A natural history comparison of SOD1-mutant patients with amyotrophic lateral sclerosis between Chinese and German populations
    Lu Tang
    Johannes Dorst
    Lu Chen
    Xiaolu Liu
    Yan Ma
    Kornelia Günther
    Sebastian Michels
    Kathrin Müller
    Axel Freischmidt
    Jochen H. Weishaupt
    Dongsheng Fan
    Albert C. Ludolph
    Translational Neurodegeneration, 10
  • [2] Better survival in female SOD1-mutant patients with ALS: a study of SOD1-related natural history
    Lu Tang
    Yan Ma
    Xiao-lu Liu
    Lu Chen
    Dong-sheng Fan
    Translational Neurodegeneration, 8
  • [3] Better survival in female SOD1-mutant patients with ALS: a study of SOD1-related natural history
    Tang, Lu
    Ma, Yan
    Liu, Xiao-lu
    Chen, Lu
    Fan, Dong-sheng
    TRANSLATIONAL NEURODEGENERATION, 2019, 8 (1)
  • [4] Mutant SOD1 mediated pathogenesis of Amyotrophic Lateral Sclerosis
    Kaur, Simran J.
    McKeown, Stephanie R.
    Rashid, Shazia
    GENE, 2016, 577 (02) : 109 - 118
  • [5] Correction to: Better survival in female SOD1-mutant patients with ALS: a study of SOD1-related natural history
    Lu Tang
    Yan Ma
    Xiao-lu Liu
    Lu Chen
    Dong-sheng Fan
    Translational Neurodegeneration, 8
  • [6] Analysis of SOD1 variants in Chinese patients with familial amyotrophic lateral sclerosis
    Li, H.
    Yuan, L.
    Yang, H.
    Guo, Y.
    Zheng, W.
    Fan, K.
    Deng, S.
    Gong, L.
    Xu, H.
    Yang, Z.
    Cheng, J.
    Kang, M.
    Deng, H.
    QJM-AN INTERNATIONAL JOURNAL OF MEDICINE, 2023, 116 (05) : 365 - 374
  • [7] Integrated transcriptomic profiling reveals a STING-mediated Type II Interferon signature in SOD1-mutant amyotrophic lateral sclerosis models
    Hiew, Jen Young
    Lim, Yi Shan
    Liu, Huitao
    Ng, Chen Seng
    COMMUNICATIONS BIOLOGY, 2025, 8 (01)
  • [8] Comparison between PFN1 and SOD1 mutations in amyotrophic lateral sclerosis
    Corcia, Philippe
    Lejeune, Pascal
    Vourc'h, Patrick
    Beltran, Stephane
    Piegay, Anne-Sophie
    Blasco, Helene
    Meininger, Vincent
    EUROPEAN JOURNAL OF NEUROLOGY, 2023, 30 (02) : 552 - 554
  • [9] Spinal cord pathology is ameliorated by P2X7 antagonism in a SOD1-mutant mouse model of amyotrophic lateral sclerosis
    Apolloni, Savina
    Amadio, Susanna
    Parisi, Chiara
    Matteucci, Alessandra
    Potenza, Rosa L.
    Armida, Monica
    Popoli, Patrizia
    D'Ambrosi, Nadia
    Volonte, Cinzia
    DISEASE MODELS & MECHANISMS, 2014, 7 (09) : 1101 - 1109
  • [10] Role of mitochondria in mutant SOD1 linked amyotrophic lateral sclerosis
    Tan, Wenzhi
    Pasinelli, Piera
    Trotti, Davide
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2014, 1842 (08): : 1295 - 1301