The genetics of PSP/CBD and FTDP-17

被引:0
|
作者
Hutton, M [1 ]
机构
[1] Mayo Clin, Jacksonville, FL 32224 USA
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
引用
收藏
页码:1402 / 1403
页数:2
相关论文
共 50 条
  • [21] Brain acetylcholinesterase activity in FTDP-17 studied by PET
    Hirano, S
    Shinotoh, H
    Kobayashi, T
    Tsuboi, Y
    Wszolek, ZK
    Aotsuka, A
    Tanaka, N
    Ota, T
    Fukushi, K
    Tanada, S
    Irie, T
    NEUROLOGY, 2006, 66 (08) : 1276 - 1277
  • [22] MAPT mutation associated with frontotemporal dementia and parkinsonism (FTDP-17)
    Haussmann, Robert
    Wysocki, Marek
    Brandt, Moritz D.
    Hermann, Andreas
    Donix, Markus
    INTERNATIONAL PSYCHOGERIATRICS, 2017, 29 (05) : 869 - 871
  • [23] Effects of FTDP-17 mutations of tau on the functions of tau.
    Licher, F
    Barghorn, S
    von Bergen, M
    Zheng-Fischhofer, Q
    Ackmann, M
    Wiech, H
    Mandelkow, EM
    Mandelkow, E
    MOLECULAR BIOLOGY OF THE CELL, 1999, 10 : 374A - 374A
  • [24] A novel deletion in progranulin gene is associated with FTDP-17 and CBS
    Benussi, Luisa
    Binetti, Giuliano
    Sina, Elena
    Gigola, Lara
    Bettecken, Thomas
    Meitinger, Thomas
    Ghidoni, Roberta
    NEUROBIOLOGY OF AGING, 2008, 29 (03) : 427 - 435
  • [25] Sleep Architecture Changed Without RBD in Patients With FTDP-17
    Liu, Jia
    Zhan, Shuqin
    Huang, Chaoyang
    Liu, Yang
    Liu, Lin
    Wu, Liyong
    Wang, Yuping
    JOURNAL OF CLINICAL SLEEP MEDICINE, 2018, 14 (10): : 1735 - 1739
  • [26] Gene expression and proteomic profiles of FTDP-17: Preliminary analyses
    Murrell, Jill
    Schweitzer, Kelly
    McClintick, Jeanette
    Decker, Emily
    Spina, Salvatore
    Wang, Mu
    Edenberg, Howard
    Ghetti, Bernardino
    BRAIN PATHOLOGY, 2006, 16 : S45 - S45
  • [27] Partial Deletion of the MAPT Gene: A Novel Mechanism of FTDP-17
    Rovelet-Lecrux, Anne
    Lecourtois, Magalie
    Thomas-Anterion, Catherine
    Le Ber, Isabelle
    Brice, Alexis
    Frebourg, Thierry
    Hannequin, Didier
    Campion, Dominique
    HUMAN MUTATION, 2009, 30 (04) : E591 - E602
  • [28] Biochemical and immunocytochemical study on FTDP-17 - From patients to mice
    Miyasaka, T
    Tatebayashi, Y
    Morishima, M
    Takashima, A
    Ihara, Y
    JOURNAL OF PHARMACOLOGICAL SCIENCES, 2004, 94 : 59P - 59P
  • [29] Olfactory dysfunction in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)
    Robowski, P.
    Slawek, J.
    Narozanska, E.
    Schinwelski, M.
    Sitek, E. J.
    Kucharska, W.
    Brockhuis, B.
    Lass, P.
    Wieczorek, D.
    Dubaniewicz, M.
    Jasinska-Myga, B.
    Baker, M. C.
    Rademakers, R.
    Wszolek, Z. K.
    MOVEMENT DISORDERS, 2009, 24 : S174 - S175
  • [30] Atypical and slowly progressive FTDP-17 caused by MAPT p. R406W mutations - similarities to AD and PSP
    Ygland, E.
    van Westen, D.
    Englund, E.
    Rademakers, R.
    Wszolek, Z.
    Nilsson, K.
    Nilsson, C.
    Hansson, O.
    Gustafson, L.
    Puschmann, A.
    MOVEMENT DISORDERS, 2017, 32