SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    S. Klebe, G. Stevanin, C. Depienne, Clinical and genetic heterogeneity in hereditary spastic paraplegias: From SPG1 to SPG72 and still counting, Revue Neurologique, 2015, 171, 6-7, 505

    CrossRef

  2. 2
    Temistocle Lo Giudice, Federica Lombardi, Filippo Maria Santorelli, Toshitaka Kawarai, Antonio Orlacchio, Hereditary spastic paraplegia: Clinical-genetic characteristics and evolving molecular mechanisms, Experimental Neurology, 2014, 261, 518

    CrossRef

  3. 3
    Yingying Luo, Juan Du, Zixiong Zhan, Chong Chen, Junling Wang, Yiqiao Hu, Zhengmao Hu, Kun Xia, Beisha Tang, Lu Shen, A diagnostic gene chip for hereditary spastic paraplegias, Brain Research Bulletin, 2013, 97, 112

    CrossRef

  4. 4
    Maria Martinez-Lage, Laura Molina-Porcel, Dana Falcone, Leo McCluskey, Virginia M.-Y. Lee, Vivianna M. Van Deerlin, John Q. Trojanowski, TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation, Acta Neuropathologica, 2012, 124, 2, 285

    CrossRef

  5. 5
    Juan Du, Ya-cen Hu, Bei-sha Tang, Chong Chen, Ying-ying Luo, Zi-xiong Zhan, Guo-hua Zhao, Hong Jiang, Kun Xia, Lu Shen, Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1, Clinical Neurology and Neurosurgery, 2011, 113, 6, 480

    CrossRef

  6. 6
    K. Svenstrup, R. S. Møller, J. Christensen, E. Budtz-Jørgensen, M. Gilling, J. E. Nielsen, NIPA1 mutation in complex hereditary spastic paraplegia with epilepsy, European Journal of Neurology, 2011, 18, 9
  7. 7
    Shi Guo Liu, Jian Jun Zhao, Mao You Zhuang, Fei Feng Li, Qing Jun Zhang, Shang Zhi Huang, Feng Yuan Che, De Guo Lu, Shi En Liu, Ji Jun Teng, Xu Ma, Clinical and genetic study of SPG6 mutation in a Chinese family with hereditary spastic paraplegia, Journal of the Neurological Sciences, 2008, 266, 1-2, 109

    CrossRef

  8. 8
    Christian Beetz, Rebecca Schüle, Stephan Klebe, Sven Klimpe, Thomas Klopstock, Arnaud Lacour, Susanne Otto, Anne-Dorte Sperfeld, Bart van de Warrenburg, Ludger Schöls, Thomas Deufel, Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspots, Journal of the Neurological Sciences, 2008, 268, 1-2, 131

    CrossRef

  9. 9
    Satoshi Kaneko, Toshitaka Kawarai, Edwin Yip, Shabnam Salehi-Rad, Christine Sato, Antonio Orlacchio, Giorgio Bernardi, Yan Liang, Hiroshi Hasegawa, Ekaterina Rogaeva, Peter St George-Hyslop, Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia, Movement Disorders, 2006, 21, 9
  10. 10
    Paul A. James, Kevin Talbot, The molecular genetics of non-ALS motor neuron diseases, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 2006, 1762, 11-12, 986

    CrossRef