-
1
-
-
0003479599
-
-
New York, Churchill-Livingstone
-
Snowden JS, Neary D, Mann DMA: Frontotemporal Lobar Degeneration: Frontotemporal Dementia, Progressive Aphasia, Semantic Dementia. New York, Churchill-Livingstone, 1996.
-
(1996)
Frontotemporal Lobar Degeneration: Frontotemporal Dementia, Progressive Aphasia, Semantic Dementia
-
-
Snowden, J.S.1
Neary, D.2
Mann, D.M.A.3
-
2
-
-
0028223015
-
Clinical, neuropsychological and neuropathological criteria for fronto-temporal dementia
-
Brun A, Englund E, Gustafson L, Passant U, Mann DMA, Neary D: Clinical, neuropsychological and neuropathological criteria for fronto-temporal dementia. J Neurol Neurosurg Psychiatry 1994;57:416-418.
-
(1994)
J Neurol Neurosurg Psychiatry
, vol.57
, pp. 416-418
-
-
Brun, A.1
Englund, E.2
Gustafson, L.3
Passant, U.4
Mann, D.M.A.5
Neary, D.6
-
3
-
-
0031672540
-
Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria
-
Neary D, Snowden JS, Gustafson L, Passant U, Stuss D, Black S, et al: Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria. Neurology 1998;51:1546-1554.
-
(1998)
Neurology
, vol.51
, pp. 1546-1554
-
-
Neary, D.1
Snowden, J.S.2
Gustafson, L.3
Passant, U.4
Stuss, D.5
Black, S.6
-
4
-
-
0032475931
-
Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions
-
Saudou F, Finkbeiner S, Devys D, Greenberg ME: Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions. Cell 1998;95:55-66.
-
(1998)
Cell
, vol.95
, pp. 55-66
-
-
Saudou, F.1
Finkbeiner, S.2
Devys, D.3
Greenberg, M.E.4
-
5
-
-
0035061081
-
The status of 'Pick's Disease' and other tauopathies within the frontotemporal dementias
-
Manna DM, Pickering-Brown S: The status of 'Pick's Disease' and other tauopathies within the frontotemporal dementias. Neurobiol Aging 2001;22:109-111.
-
(2001)
Neurobiol Aging
, vol.22
, pp. 109-111
-
-
Manna, D.M.1
Pickering-Brown, S.2
-
6
-
-
0342470539
-
Molecular classification of the dementias
-
Mann DMA, McDonagh AM, Snowden JS, Neary D, Pickering-Brown SM: Molecular classification of the dementias. Lancet 2000;355:626-627.
-
(2000)
Lancet
, vol.355
, pp. 626-627
-
-
Mann, D.M.A.1
McDonagh, A.M.2
Snowden, J.S.3
Neary, D.4
Pickering-Brown, S.M.5
-
7
-
-
0032543684
-
Coding and 5′ splice mutations in tau associated with inherited dementia (FTDP-17)
-
Hutton M, Lendon C, Rizzu P, Baker M, Froelich S, Houlden H, Pickering-Brown SM, Chakraverty S, Isaacs A, Grover A, Hackett J, Adamson J, Lincoln S, Dickson D, Davies P, Petersen RC, Stevens M, de Graaf E, Wauter E, van Baren, Che LK, Norton J, Morris JC, Reed LA, Trojanowski JQ, Basun H, Lannfelt L, Neystat M, Fahn S, Dark F, Tannenberg T, Dodd P, Hayward N, Kwok J, Schofield P, Andreadis A, Snowden J, Craufurd D, Neary D, Owen F, Oostra B, Hardy J, Goate A, van Swieten J, Mann D, Lynch T, Heutink P: Coding and 5′ splice mutations in tau associated with inherited dementia (FTDP-17). Nature 1998;393:702-705.
-
(1998)
Nature
, vol.393
, pp. 702-705
-
-
Hutton, M.1
Lendon, C.2
Rizzu, P.3
Baker, M.4
Froelich, S.5
Houlden, H.6
Pickering-Brown, S.M.7
Chakraverty, S.8
Isaacs, A.9
Grover, A.10
Hackett, J.11
Adamson, J.12
Lincoln, S.13
Dickson, D.14
Davies, P.15
Petersen, R.C.16
Stevens, M.17
De Graaf, E.18
Wauter, E.19
Van Baren20
Che, L.K.21
Norton, J.22
Morris, J.C.23
Reed, L.A.24
Trojanowski, J.Q.25
Basun, H.26
Lannfelt, L.27
Neystat, M.28
Fahn, S.29
Dark, F.30
Tannenberg, T.31
Dodd, P.32
Hayward, N.33
Kwok, J.34
Schofield, P.35
Andreadis, A.36
Snowden, J.37
Craufurd, D.38
Neary, D.39
Owen, F.40
Oostra, B.41
Hardy, J.42
Goate, A.43
Van Swieten, J.44
Mann, D.45
Lynch, T.46
Heutink, P.47
more..
-
8
-
-
0032560487
-
Mutation in the tau gene in familial multisystem tauopathy with presenile dementia
-
Spillantini MG, Murrell JR, Goedert M, Farlow MR, Klug A, Ghetti B: Mutation in the tau gene in familial multisystem tauopathy with presenile dementia. Proc Natl Acad Sci USA 1998;95:7737-7741.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 7737-7741
-
-
Spillantini, M.G.1
Murrell, J.R.2
Goedert, M.3
Farlow, M.R.4
Klug, A.5
Ghetti, B.6
-
9
-
-
14444284106
-
Tau is a candidate gene for chromosome 17 frontotemporal dementia
-
Poorkaj P, Bird TD, Wijsman E, Nemens E, Garruto RM, Anderson L, Andreadis A, Wiederholt WC, Raskind M, Schellenberg GD: Tau is a candidate gene for chromosome 17 frontotemporal dementia. Ann Neurol 1998;43:815-826.
-
(1998)
Ann Neurol
, vol.43
, pp. 815-826
-
-
Poorkaj, P.1
Bird, T.D.2
Wijsman, E.3
Nemens, E.4
Garruto, R.M.5
Anderson, L.6
Andreadis, A.7
Wiederholt, W.C.8
Raskind, M.9
Schellenberg, G.D.10
-
11
-
-
0036205905
-
Inherited frontotemporal dementia in 9 British families associated with intronic mutations in the tau gene
-
Pickering-Brown SM, Richardson AMT, Snowden JS, McDonagh A, Burns A, Braudie W, Baker M, Yen S-H, Hardy J, Hutton M, Davies Y, Allsop D, Craufurd D, Neary D, Mann DMA: Inherited frontotemporal dementia in 9 British families associated with intronic mutations in the tau gene. Brain 2002;125:732-751.
-
(2002)
Brain
, vol.125
, pp. 732-751
-
-
Pickering-Brown, S.M.1
Richardson, A.M.T.2
Snowden, J.S.3
McDonagh, A.4
Burns, A.5
Braudie, W.6
Baker, M.7
Yen, S.-H.8
Hardy, J.9
Hutton, M.10
Davies, Y.11
Allsop, D.12
Craufurd, D.13
Neary, D.14
Mann, D.M.A.15
-
12
-
-
0036198120
-
Late-onset frontotemporal dementia with a novel exon 1 (Arg5His) tau gene mutation
-
Hayashi S, Toyoshima Y, Hasegawa M, Umeda Y, Wakabayashi K, Tokiguchi S, Iwatsubo T, Takahashi H: Late-onset frontotemporal dementia with a novel exon 1 (Arg5His) tau gene mutation. Ann Neurol 2002;51:525-530.
-
(2002)
Ann Neurol
, vol.51
, pp. 525-530
-
-
Hayashi, S.1
Toyoshima, Y.2
Hasegawa, M.3
Umeda, Y.4
Wakabayashi, K.5
Tokiguchi, S.6
Iwatsubo, T.7
Takahashi, H.8
-
13
-
-
0032837303
-
Frequency of tau mutations in three series on non-Alzheimer's degenerative dementia
-
Houlden H, Baker M, Adamson J, Grover A, Waring S, Dickson D, Lynch T, Boeve B, Peterson R, Pickering-Brown S, Owen F, Neary D, Craufurd D, Snowden J, Mann D, Hutton M: Frequency of tau mutations in three series on non-Alzheimer's degenerative dementia. Ann Neurology 1999;46:243-248.
-
(1999)
Ann Neurology
, vol.46
, pp. 243-248
-
-
Houlden, H.1
Baker, M.2
Adamson, J.3
Grover, A.4
Waring, S.5
Dickson, D.6
Lynch, T.7
Boeve, B.8
Peterson, R.9
Pickering-Brown, S.10
Owen, F.11
Neary, D.12
Craufurd, D.13
Snowden, J.14
Mann, D.15
Hutton, M.16
-
14
-
-
0035108754
-
Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia
-
Poorkaj P, Grossman M, Steinbart E, Payami H, Sadovnick A, Nochlin D, Tabira T, Trojanowski JQ, Borson S, Galasko D, Reich S, Quinn B, Schellenberg G, Bird TD: Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia. Arch Neurol 2001;58:383-387.
-
(2001)
Arch Neurol
, vol.58
, pp. 383-387
-
-
Poorkaj, P.1
Grossman, M.2
Steinbart, E.3
Payami, H.4
Sadovnick, A.5
Nochlin, D.6
Tabira, T.7
Trojanowski, J.Q.8
Borson, S.9
Galasko, D.10
Reich, S.11
Quinn, B.12
Schellenberg, G.13
Bird, T.D.14
-
15
-
-
0037161233
-
Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation
-
Janssen JC, Warrington EK, Morris HR, Lantos P, Brown J, Revesz T, Wood N, Khan MN, Cipolotti L, Fox NC, Rossor MN: Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation. Neurology 2002;8:1161-1168.
-
(2002)
Neurology
, vol.8
, pp. 1161-1168
-
-
Janssen, J.C.1
Warrington, E.K.2
Morris, H.R.3
Lantos, P.4
Brown, J.5
Revesz, T.6
Wood, N.7
Khan, M.N.8
Cipolotti, L.9
Fox, N.C.10
Rossor, M.N.11
-
16
-
-
2642585172
-
Evidence of a founder effect in families of frontotemporal dementia that harbour the tau +16 splice mutation
-
in press
-
Pickering-Brown SM, Baker M, Bird T, Trojanowski J, Lee V, Morris H, Rossor M, Jannssen JC, Neary D, Craufurd D, Richardson A, Snowden J, Hardy J, Mann D, Hutton M: Evidence of a founder effect in families of frontotemporal dementia that harbour the tau +16 splice mutation. Am J Med Genet, in press.
-
Am J Med Genet
-
-
Pickering-Brown, S.M.1
Baker, M.2
Bird, T.3
Trojanowski, J.4
Lee, V.5
Morris, H.6
Rossor, M.7
Jannssen, J.C.8
Neary, D.9
Craufurd, D.10
Richardson, A.11
Snowden, J.12
Hardy, J.13
Mann, D.14
Hutton, M.15
-
17
-
-
0035138764
-
Loss of brain tau defines novel sporadic and familial tauopathies with frontotemporal dementia
-
Zhukareva V, Vogelsberg-Ragaglia V, Van Deerlin VM, Bruce J, Shuck T, Grossman M, Clark CM, Arnold SE, Masliah E, Galasko D, Trojanowski JQ, Lee VM: Loss of brain tau defines novel sporadic and familial tauopathies with frontotemporal dementia. Ann Neurol 2001;49:165-175.
-
(2001)
Ann Neurol
, vol.49
, pp. 165-175
-
-
Zhukareva, V.1
Vogelsberg-Ragaglia, V.2
Van Deerlin, V.M.3
Bruce, J.4
Shuck, T.5
Grossman, M.6
Clark, C.M.7
Arnold, S.E.8
Masliah, E.9
Galasko, D.10
Trojanowski, J.Q.11
Lee, V.M.12
-
18
-
-
0842265475
-
The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein
-
in press
-
Taniguchi S, McDonagh AM, Pickering-Brown SM, Umeda Y, Iwatsubo T, Hasegawa M, Mann DM: The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein. Neuropathol Appl Neurobiol, in press.
-
Neuropathol Appl Neurobiol
-
-
Taniguchi, S.1
McDonagh, A.M.2
Pickering-Brown, S.M.3
Umeda, Y.4
Iwatsubo, T.5
Hasegawa, M.6
Mann, D.M.7
-
19
-
-
0035940833
-
Tau protein expression in frontotemporal dementias
-
Adamec E, Chang HT, Stopa EG, Hedreen JC, Vonsattel JP: Tau protein expression in frontotemporal dementias. Neurosci Lett 2001;315:21-24.
-
(2001)
Neurosci Lett
, vol.315
, pp. 21-24
-
-
Adamec, E.1
Chang, H.T.2
Stopa, E.G.3
Hedreen, J.C.4
Vonsattel, J.P.5
-
20
-
-
0030757803
-
Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21
-
Froelich S, Basun H, Forsell C, Lilius L, Axelman K, Andreadis A, Lannfelt L: Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21. Am J Med Genet 1997;74:380-385.
-
(1997)
Am J Med Genet
, vol.74
, pp. 380-385
-
-
Froelich, S.1
Basun, H.2
Forsell, C.3
Lilius, L.4
Axelman, K.5
Andreadis, A.6
Lannfelt, L.7
-
21
-
-
0034784189
-
Familial frontotemporal dementia with ubiquitin-positive inclusions linked to chromosome 17q21-22
-
Rosso SM, Kamphorst W, deGraaf B, Willemsen R, Ravid R, Niermeijer MF, Spillantini MG, Heutink P, Van Swieten JC: Familial frontotemporal dementia with ubiquitin-positive inclusions linked to chromosome 17q21-22. Brain 2001;124:1948-1957.
-
(2001)
Brain
, vol.124
, pp. 1948-1957
-
-
Rosso, S.M.1
Kamphorst, W.2
DeGraaf, B.3
Willemsen, R.4
Ravid, R.5
Niermeijer, M.F.6
Spillantini, M.G.7
Heutink, P.8
Van Swieten, J.C.9
-
22
-
-
12244259054
-
Tau-negative frontal lobe dementia at 17q21: Significant finemapping of the candidate region to a 4.8-cm interval
-
Rademakers R, Cruts M, Dermaut B, Sleegers K, Rosso SM, Van Den Broeck M, Backhovens H, Van Swieten J, Van Duijn CM, Van Broeckhoven C: Tau-negative frontal lobe dementia at 17q21: Significant finemapping of the candidate region to a 4.8-cm interval. Mol Psychiatry 2002;7:1064-1074.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 1064-1074
-
-
Rademakers, R.1
Cruts, M.2
Dermaut, B.3
Sleegers, K.4
Rosso, S.M.5
Van Den Broeck, M.6
Backhovens, H.7
Van Swieten, J.8
Van Duijn, C.M.9
Van Broeckhoven, C.10
-
23
-
-
0031799683
-
Hereditary dysphasic disinhibition dementia: A frontotemporal dementia linked to 17q21-22
-
Lendon CL, Lynch T, Norton J, McKeel DW Jr, Busfield F, Craddock N, Chakraverty S, Gopalakrishnan G, Shears SD, Grimmett W, Wilhelmsen KC, Hansen L, Morris JC, Goate AM: Hereditary dysphasic disinhibition dementia: A frontotemporal dementia linked to 17q21-22. Neurology 1998;50:1546-1555.
-
(1998)
Neurology
, vol.50
, pp. 1546-1555
-
-
Lendon, C.L.1
Lynch, T.2
Norton, J.3
McKeel Jr., D.W.4
Busfield, F.5
Craddock, N.6
Chakraverty, S.7
Gopalakrishnan, G.8
Shears, S.D.9
Grimmett, W.10
Wilhelmsen, K.C.11
Hansen, L.12
Morris, J.C.13
Goate, A.M.14
-
24
-
-
0042821633
-
Extended investigation of tau and mutation screening of other candidate genes on chromosome 17q21 in a Swedish FTDP-17 family
-
Froelich-Fabre S, Axelman P, Almkvist A, Basun H, Lannfelt L: Extended investigation of tau and mutation screening of other candidate genes on chromosome 17q21 in a Swedish FTDP-17 family. Am J Med Genet 2003;121B:112-118.
-
(2003)
Am J Med Genet
, vol.121 B
, pp. 112-118
-
-
Froelich-Fabre, S.1
Axelman, P.2
Almkvist, A.3
Basun, H.4
Lannfelt, L.5
-
25
-
-
0026488111
-
Structure and novel exons of the human τgene
-
Andreadis A, Brown WM, Kosik KS: Structure and novel exons of the human τgene. Biochemistry 1992;31:10626-10633.
-
(1992)
Biochemistry
, vol.31
, pp. 10626-10633
-
-
Andreadis, A.1
Brown, W.M.2
Kosik, K.S.3
-
26
-
-
0024387161
-
Cloning and sequencing of the cDNA encoding an isoform of microtubuleassociated protein tau containing four tandem repeats: Differential expression of tau protein mRNAs in human brain
-
Goedert M, Spillantini MG, Potier MC, Ulrich J, Crowther RA: Cloning and sequencing of the cDNA encoding an isoform of microtubuleassociated protein tau containing four tandem repeats: Differential expression of tau protein mRNAs in human brain. EMBO J 1989;8:393-399.
-
(1989)
EMBO J
, vol.8
, pp. 393-399
-
-
Goedert, M.1
Spillantini, M.G.2
Potier, M.C.3
Ulrich, J.4
Crowther, R.A.5
-
27
-
-
0242317909
-
Mutations in the tau gene that cause an increase in three repeat tau and frontotemporal dementia
-
Stanford PM, Shepherd CE, Halliday GM, Brooks WS, Schofield PW, Brodaty H, Martins RN, Kwok JB, Schofield PR: Mutations in the tau gene that cause an increase in three repeat tau and frontotemporal dementia. Brain 2003;126:814-826.
-
(2003)
Brain
, vol.126
, pp. 814-826
-
-
Stanford, P.M.1
Shepherd, C.E.2
Halliday, G.M.3
Brooks, W.S.4
Schofield, P.W.5
Brodaty, H.6
Martins, R.N.7
Kwok, J.B.8
Schofield, P.R.9
-
28
-
-
0033545946
-
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements
-
D'Souza I, Poorkaj P, Hong M, Nochlin D, Lee VM-Y, Bird TD: Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements. Proc Natl Acad Sci USA 1999;96:5598-5603.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 5598-5603
-
-
D'Souza, I.1
Poorkaj, P.2
Hong, M.3
Nochlin, D.4
Lee, V.M.-Y.5
Bird, T.D.6
-
29
-
-
0033669232
-
Pick's disease is associated with mutations in the tau gene
-
Pickering-Brown S, Baker M, Yen SH, Liu WK, Hasegawa M, Cairns N, Lantos PL, Rossor M, Iwatsubo T, Davies Y, Allsop D, Furlong R, Owen F, Hardy J, Mann D, Hutton M: Pick's disease is associated with mutations in the tau gene. Ann Neurol 2000;48:859-867.
-
(2000)
Ann Neurol
, vol.48
, pp. 859-867
-
-
Pickering-Brown, S.1
Baker, M.2
Yen, S.H.3
Liu, W.K.4
Hasegawa, M.5
Cairns, N.6
Lantos, P.L.7
Rossor, M.8
Iwatsubo, T.9
Davies, Y.10
Allsop, D.11
Furlong, R.12
Owen, F.13
Hardy, J.14
Mann, D.15
Hutton, M.16
-
30
-
-
0032763203
-
Tau gene mutation G389R causes a tauopathy with abundant Pick body-like inclusions and axonal deposits
-
Murrell J, Spillantini M, Zolo P, Guazzelli M, Smith M, Hasegawa M, Redi F, Crowther, R, Pietrini P, Ghetti B, Goedert M: Tau gene mutation G389R causes a tauopathy with abundant Pick body-like inclusions and axonal deposits. J Neuropathol Exp Neurol 1999;58:1207-1226.
-
(1999)
J Neuropathol Exp Neurol
, vol.58
, pp. 1207-1226
-
-
Murrell, J.1
Spillantini, M.2
Zolo, P.3
Guazzelli, M.4
Smith, M.5
Hasegawa, M.6
Redi, F.7
Crowther, R.8
Pietrini, P.9
Ghetti, B.10
Goedert, M.11
-
31
-
-
0025330687
-
Prion dementia without characteristic pathology
-
Collinge J, Owen F, Poulter M, Leach M, Crow TJ, Rossor MN, Hardy J, Mullan MJ, Janota I, Lantos PL: Prion dementia without characteristic pathology. Lancet 1990;336:7-9.
-
(1990)
Lancet
, vol.336
, pp. 7-9
-
-
Collinge, J.1
Owen, F.2
Poulter, M.3
Leach, M.4
Crow, T.J.5
Rossor, M.N.6
Hardy, J.7
Mullan, M.J.8
Janota, I.9
Lantos, P.L.10
|