Late-onset hereditary spastic paraplegia with thin corpus callosum caused by a new SPG3A mutation

被引：0
|
作者：
Antonio Orlacchio
Pasqua Montieri
Carla Babalini
Fabrizio Gaudiello
Giorgio Bernardi
Toshitaka Kawarai
机构：
[1] Centro Europeo di Ricerca sul Cervello (CERC),Laboratorio di Neurogenetica
[2] Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Santa Lucia,Dipartimento di Neuroscienze
[3] Università di Roma “Tor Vergata”,Department of Neurology
[4] Hyogo Brain and Heart Center,undefined
来源：
Journal of Neurology | 2011年 / 258卷
关键词：
Hereditary Spastic Paraplegia; Autosomal Dominant; Thin Corpus Callosum; Atypical Clinical Characteristic; Sphincter Incompetence;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：1361 / 1363
页数：2
相关论文
共 50 条
  • [1] Hereditary spastic paraplegia with thin corpus callosum and SPG11 mutation: A neuropathological evaluation
    Scherpelz, Kathryn P.
    Yoda, Rebecca A.
    Jayadev, Suman
    Davis, Marie Y.
    Hincks, Joshua C.
    Liachko, Nicole F.
    Bragg, Robert M.
    Cochoit, Alexa
    MacDonald, Christine L.
    Keene, C. Dirk
    Bird, Thomas D.
    Latimer, Caitlin S.
    NEUROPATHOLOGY, 2024, : 123 - 134
  • [2] SPG3A gene polymorphisms in hereditary spastic paraplegia
    Li, Tian
    Tu, Li
    Zhang, Qian
    Gu, Ran
    Wang, Qian
    Wang, Bingjin
    Yao, Huan
    Qu, Xiang
    Wang, Wenqin
    Tian, Jinyong
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2017, 10 (09): : 9760 - 9764
  • [3] Atypical late-onset hereditary spastic paraplegia with thin corpus callosum due to novel compound heterozygous mutations in the SPG11 gene
    Maria Pia Giannoccaro
    Rocco Liguori
    Alessia Arnoldi
    Vincenzo Donadio
    Patrizia Avoni
    Maria Teresa Bassi
    Journal of Neurology, 2014, 261 : 1825 - 1827
  • [4] A novel mutation in the SPG3A gene (atlastin) in hereditary spastic paraplegia
    M. Matsui
    T. Kawarai
    Y. Hase
    H. Tomimoto
    K. Iseki
    E. Rogaeva
    A. Orlacchio
    G. Bernardi
    P. St. George-Hyslop
    R. Takahashi
    M. Matsui
    Journal of Neurology, 2007, 254 : 972 - 974
  • [5] Atypical late-onset hereditary spastic paraplegia with thin corpus callosum due to novel compound heterozygous mutations in the SPG11 gene
    Giannoccaro, Maria Pia
    Liguori, Rocco
    Arnoldi, Alessia
    Donadio, Vincenzo
    Avoni, Patrizia
    Bassi, Maria Teresa
    JOURNAL OF NEUROLOGY, 2014, 261 (09) : 1825 - 1827
  • [6] Atypical hereditary spastic paraplegia with thin corpus callosum in a Korean patient with a novel SPG11 mutation
    Yoon, W. T.
    Lee, W. Y.
    Lee, S. -T.
    Ahn, J. Y.
    Ki, C. -S.
    Cho, J. W.
    EUROPEAN JOURNAL OF NEUROLOGY, 2012, 19 (01) : e7 - e8
  • [7] Spastizin mutation in hereditary spastic paraplegia with thin corpus callosum
    Sanjiban Chakrabarty
    Nimish Vijayakumar
    Kurupath Radhakrishnan
    Kapaettu Satyamoorthy
    Journal of Neurology, 2016, 263 : 2130 - 2132
  • [8] Novel SPG 11 Mutations in Hereditary Spastic Paraplegia With Thin Corpus Callosum in a Chinese Family
    Tian, Xiaojie
    Wang, Min
    Zhang, Kaiyuan
    Zhang, Xinqing
    CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 2016, 43 (06) : 833 - 840
  • [9] Hereditary spastic paraplegia with a thin corpus callosum
    Sivaraman Somasundaram
    Seetharam Raghavendra
    Atampreet Singh
    Chandrasekharan Kesavadas
    Muraleedharan Nair
    Pediatric Radiology, 2007, 37 : 503 - 505
  • [10] Hereditary spastic paraplegia with a thin corpus callosum
    Somasundaram, Sivaraman
    Raghavendra, Seetharam
    Singh, Atampreet
    Kesavadas, Chandrasekharan
    Nair, Muraleedharan
    PEDIATRIC RADIOLOGY, 2007, 37 (05) : 503 - 505
12345