Another phenotype of frontotemporal dementia and parkinsonism linked to chromosome-17 (FTDP17) with a missense mutation of S305N closely resembling Pick's disease

被引：16

作者：

Kobayashi, K

Kidani, T

Ujike, H

Hayashi, M

Ishihara, T

Miyazu, K

Kuroda, S

Koshino, Y

机构：

[1] Kanazawa Univ, Dept Psychiat & Neurobiol, Grad Sch Med Sci, Kanazawa, Ishikawa 9208641, Japan

[2] Okayama Univ, Dept Neuropsychiat, Grad Sch Med Sci, Okayama 7008530, Japan

[3] Natl Hokuriku Hosp, Dept Neuropsychiat, Jouhana, Toyama 9391893, Japan

来源：

JOURNAL OF NEUROLOGY | 2003年 / 250卷 / 08期

关键词：

D O I：

10.1007/s00415-003-1137-6

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：990 / 992

页数：3

共 20 条

[1]

Arai T, 2001, ACTA NEUROPATHOL, V101, P167

[2]

Buée L, 1999, BRAIN PATHOL, V9, P681

[3]

Ghetti B, 2000, ANN NY ACAD SCI, V920, P52

[4] FTDP-17 mutations N279K and S305N in tau produce increased splicing of exon 10 [J].

Hasegawa, M ;

Smith, MJ ;

Iijima, M ;

Tabira, T ;

Goedert, M .

FEBS LETTERS, 1999, 443 (02) :93-96

[5] Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 [J].

Hutton, M ;

Lendon, CL ;

Rizzu, P ;

Baker, M ;

Froelich, S ;

Houlden, H ;

Pickering-Brown, S ;

Chakraverty, S ;

Isaacs, A ;

Grover, A ;

Hackett, J ;

Adamson, J ;

Lincoln, S ;

Dickson, D ;

Davies, P ;

Petersen, RC ;

Stevens, M ;

de Graaff, E ;

Wauters, E ;

van Baren, J ;

Hillebrand, M ;

Joosse, M ;

Kwon, JM ;

Nowotny, P ;

Che, LK ;

Norton, J ;

Morris, JC ;

Reed, LA ;

Trojanowski, J ;

Basun, H ;

Lannfelt, L ;

Neystat, M ;

Fahn, S ;

Dark, F ;

Tannenberg, T ;

Dodd, PR ;

Hayward, N ;

Kwok, JBJ ;

Schofield, PR ;

Andreadis, A ;

Snowden, J ;

Craufurd, D ;

Neary, D ;

Owen, F ;

Oostra, BA ;

Hardy, J ;

Goate, A ;

van Swieten, J ;

Mann, D ;

Lynch, T .

NATURE, 1998, 393 (6686) :702-705

[6] A distinct familial presenile dementia with a novel missense mutation in the tau gene [J].

Iijima, M ;

Tabira, T ;

Poorkaj, P ;

Schellenberg, GD ;

Trojanowski, JQ ;

Lee, VMY ;

Schmidt, ML ;

Takahashi, K ;

Nabika, T ;

Matsumoto, T ;

Yamashita, Y ;

Yoshioka, S ;

Ishino, H .

NEUROREPORT, 1999, 10 (03) :497-501

[7] Pick-body-like inclusions in corticobasal degeneration differ from Pick bodies in Pick's disease [J].

Ikeda, K ;

Akiyama, H ;

Arai, T ;

Tsuchiya, K .

ACTA NEUROPATHOLOGICA, 2002, 103 (02) :115-118

[8]

Kobayashi K, 2002, CLIN NEUROPATHOL, V21, P191

[9]

Kobayashi K, 1999, CLIN NEUROPATHOL, V18, P240

[10] Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits [J].

Murrell, JR ;

Spillantini, MG ;

Zolo, P ;

Guazzelli, M ;

Smith, MJ ;

Hasegawa, M ;

Redi, F ;

Crowther, RA ;

Pietrini, P ;

Ghetti, B ;

Goedert, M .

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1999, 58 (12) :1207-1226

← 1 2 →