-
1
-
-
34848906841
-
Focal cortical presentations of Alzheimer's disease
-
Alladi S, Xuereb J, Bak T, Nestor P, Knibb J, Patterson K, Hodges JR. 2007. Focal cortical presentations of Alzheimer's disease. Brain 130: 2636-2645.
-
(2007)
Brain
, vol.130
, pp. 2636-2645
-
-
Alladi, S.1
Xuereb, J.2
Bak, T.3
Nestor, P.4
Knibb, J.5
Patterson, K.6
Hodges, J.R.7
-
2
-
-
0000293742
-
Über eine eigenartige Erkrankung der Hirnrinde
-
Alzheimer A. 1907. Über eine eigenartige Erkrankung der Hirnrinde. Allg Z Psychiat 64: 146-148.
-
(1907)
Allg Z Psychiat
, vol.64
, pp. 146-148
-
-
Alzheimer, A.1
-
3
-
-
33646906138
-
Über eigenartige Krankheitsfälle des späteren Alters
-
Alzheimer A. 1911. Über eigenartige Krankheitsfälle des späteren Alters. Z ges Neurol Psychiat 4: 356-385.
-
(1911)
Z ges Neurol Psychiat
, vol.4
, pp. 356-385
-
-
Alzheimer, A.1
-
4
-
-
34249949338
-
TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease
-
Amador-Ortiz C, Lin WL, Ahmed Z, Personett D, Davies P, Duara R, Graff-Radford NR, Hutton ML, Dickson DW. 2007. TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease. Ann Neurol 61: 435-445.
-
(2007)
Ann Neurol
, vol.61
, pp. 435-445
-
-
Amador-Ortiz, C.1
Lin, W.L.2
Ahmed, Z.3
Personett, D.4
Davies, P.5
Duara, R.6
Graff-Radford, N.R.7
Hutton, M.L.8
Dickson, D.W.9
-
5
-
-
33750716074
-
TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Arai T, Hasegawa M, Akiyama H, Ikeda K, Nonaka T, Mori H, Mann D, TsuchiyaK, Yoshida M, Hashizume Y, et al. 2006. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem Biophys Res Commun 351: 602-611.
-
(2006)
Biochem Biophys Res Commun
, vol.351
, pp. 602-611
-
-
Arai, T.1
Hasegawa, M.2
Akiyama, H.3
Ikeda, K.4
Nonaka, T.5
Mori, H.6
Mann, D.7
Tsuchiya, K.8
Yoshida, M.9
Hashizume, Y.10
-
6
-
-
34548146119
-
Immunotherapy targeting pathological tau conformers in a transgenic mouse model reduces brain pathology associated with functional improvements
-
Asuni AA, Boutajangout A, Quatermain D, Sigurdsson EM. 2007. Immunotherapy targeting pathological tau conformers in a transgenic mouse model reduces brain pathology associated with functional improvements. J Neurosci 27: 9115-9129.
-
(2007)
J Neurosci
, vol.27
, pp. 9115-9129
-
-
Asuni, A.A.1
Boutajangout, A.2
Quatermain, D.3
Sigurdsson, E.M.4
-
7
-
-
78751616191
-
TDP-43 regulates its mRNA levels through a negative feedback loop
-
Ayala YM, De Conti L, Avendano-Vázquez SE, Dhir A, Romano M, D'AmbrogioA, Tollervey J, Ule J, Baralle M, Buratti E, et al. 2011. TDP-43 regulates its mRNA levels through a negative feedback loop. EMBO J 30: 277-288.
-
(2011)
EMBO J
, vol.30
, pp. 277-288
-
-
Ayala, Y.M.1
De Conti, L.2
Avendano-Vázquez, S.E.3
Dhir, A.4
Romano, M.5
D'Ambrogio, A.6
Tollervey, J.7
Ule, J.8
Baralle, M.9
Buratti, E.10
-
8
-
-
33746919083
-
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
-
Baker M, Mackenzie IR, Pickering-Brown SM, Gass J, Rademakers R, LindholmC, Snowden J, Adamson J, Sadovnick AD, Rollinson S, et al. 2006. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 442: 916-919.
-
(2006)
Nature
, vol.442
, pp. 916-919
-
-
Baker, M.1
McKenzie, I.R.2
Pickering-Brown, S.M.3
Gass, J.4
Rademakers, R.5
Lindholm, C.6
Snowden, J.7
Adamson, J.8
Sadovnick, A.D.9
Rollinson, S.10
-
9
-
-
65649112431
-
TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration
-
Benajiba L, Le Ber I, Camuzat A, Lacoste M, Thomas-Anterion C, Couratier P, Legallic S, Salachas F, Hannequin D, Decousus M, et al. 2009. TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration. Ann Neurol 65: 470-474.
-
(2009)
Ann Neurol
, vol.65
, pp. 470-474
-
-
Benajiba, L.1
Le Ber, I.2
Camuzat, A.3
Lacoste, M.4
Thomas-Anterion, C.5
Couratier, P.6
Legallic, S.7
Salachas, F.8
Hannequin, D.9
Decousus, M.10
-
10
-
-
51849170227
-
Die umschriebene Atrophie der Basalganglien
-
Bonfiglio F. 1938. Die umschriebene Atrophie der Basalganglien. Z Neurol 160: 306-333.
-
(1938)
Z Neurol
, vol.160
, pp. 306-333
-
-
Bonfiglio, F.1
-
11
-
-
79451471618
-
The pathological process underlying Alzheimer's disease in individuals under thirty
-
Braak H, Del Tredici K. 2011. The pathological process underlying Alzheimer's disease in individuals under thirty. Acta Neuropathol 121: 171-181.
-
(2011)
Acta Neuropathol
, vol.121
, pp. 171-181
-
-
Braak, H.1
Del Tredici, K.2
-
12
-
-
0022257253
-
Mise en évidence immunologique de la protéine tau au niveau des lésions de dégénérescence neurofibrillaire de la maladie d'Alzheimer
-
Brion JP, Passareiro H, Nunez J, Flament-Durand J. 1985. Mise en évidence immunologique de la protéine tau au niveau des lésions de dégénérescence neurofibrillaire de la maladie d'Alzheimer. Arch Biol 95: 229-235.
-
(1985)
Arch Biol
, vol.95
, pp. 229-235
-
-
Brion, J.P.1
Passareiro, H.2
Nunez, J.3
Flament-Durand, J.4
-
13
-
-
0000841832
-
Perte de la parole, ramollissement chronique et destruction partielle du lobe antérieur gauche du cerveau
-
Broca P. 1861. Perte de la parole, ramollissement chronique et destruction partielle du lobe antérieur gauche du cerveau. Bull Soc Anthropol 2: 235-238.
-
(1861)
Bull Soc Anthropol
, vol.2
, pp. 235-238
-
-
Broca, P.1
-
14
-
-
0023202914
-
Frontal lobe degeneration of non-Alzheimer type. I. Neuropathology
-
Brun A. 1987. Frontal lobe degeneration of non-Alzheimer type. I. Neuropathology. Arch Gerontol Geriatr 6: 193-208.
-
(1987)
Arch Gerontol Geriatr
, vol.6
, pp. 193-208
-
-
Brun, A.1
-
15
-
-
0033059975
-
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in Tau
-
Bugiani O, Murrell JR, Giaccone G, Hasegawa M, Ghigo G, Tabaton M, MorbinM, Primavera A, Carella F, Solaro C, et al. 1999. Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in Tau. J Neuropathol Exp Neurol 58: 667-677.
-
(1999)
J Neuropathol Exp Neurol
, vol.58
, pp. 667-677
-
-
Bugiani, O.1
Murrell, J.R.2
Giaccone, G.3
Hasegawa, M.4
Ghigo, G.5
Tabaton, M.6
Morbin, M.7
Primavera, A.8
Carella, F.9
Solaro, C.10
-
16
-
-
33845361007
-
Haplotype-specific expression of exon 10 at the human MAPT locus
-
Caffrey TM, Joachim C, Paracchini S, Esiri MM, Wade-Martins R. 2006. Haplotype-specific expression of exon 10 at the human MAPT locus. Hum Mol Genet 15: 3529-3537.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 3529-3537
-
-
Caffrey, T.M.1
Joachim, C.2
Paracchini, S.3
Esiri, M.M.4
Wade-Martins, R.5
-
17
-
-
67650077008
-
Transmission and spreading of tauopathy in transgenic mouse brain
-
Clavaguera F, Bolmont T, Crowther RA, Abramowski D, Frank S, Probst A, Fraser G, Stalder AK, Beibel M, Staufenbiel M, et al. 2009. Transmission and spreading of tauopathy in transgenic mouse brain. Nat Cell Biol 11: 909-913.
-
(2009)
Nat Cell Biol
, vol.11
, pp. 909-913
-
-
Clavaguera, F.1
Bolmont, T.2
Crowther, R.A.3
Abramowski, D.4
Frank, S.5
Probst, A.6
Fraser, G.7
Stalder, A.K.8
Beibel, M.9
Staufenbiel, M.10
-
19
-
-
0016211732
-
Pick's disease. Histological and clinical correlations
-
Constantinidis J, Richard J, Tissot R. 1974. Pick's disease. Histological and clinical correlations. Eur Neurol 11: 208-217.
-
(1974)
Eur Neurol
, vol.11
, pp. 208-217
-
-
Constantinidis, J.1
Richard, J.2
Tissot, R.3
-
20
-
-
77952418165
-
Modeling familial Danish dementia in mice supports the concept of the amyloid hypothesis of Alzheimer's disease
-
Coomaraswamy J, Kilger E, Wölfing H, Schäfer C, Kaeser SA, Wegenast-BraunBM, Hefendehl JK, Wolburg H, Mazzella M, Ghiso J, et al. 2010. Modeling familial Danish dementia in mice supports the concept of the amyloid hypothesis of Alzheimer's disease. Proc Natl Acad Sci 107: 7969-7974.
-
(2010)
Proc Natl Acad Sci
, vol.107
, pp. 7969-7974
-
-
Coomaraswamy, J.1
Kilger, E.2
Wölfing, H.3
Schäfer, C.4
Kaeser, S.A.5
Wegenast-Braun, B.M.6
Hefendehl, J.K.7
Wolburg, H.8
Mazzella, M.9
Ghiso, J.10
-
21
-
-
0033850080
-
Abnormal tau-containing filaments in neurodegenerative diseases
-
Crowther RA, Goedert M. 2000. Abnormal tau-containing filaments in neurodegenerative diseases. J Struct Biol 130: 271-279.
-
(2000)
J Struct Biol
, vol.130
, pp. 271-279
-
-
Crowther, R.A.1
Goedert, M.2
-
22
-
-
33746910649
-
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
-
Cruts M, Gijselinck I, van der Zee J, Engelborghs S, Wils H, Pirici D, Rademakers R, Vandenberghe R, Dermaut B, Martin JJ, et al. 2006. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 442: 920-924.
-
(2006)
Nature
, vol.442
, pp. 920-924
-
-
Cruts, M.1
Gijselinck, I.2
van der Zee, J.3
Engelborghs, S.4
Wils, H.5
Pirici, D.6
Rademakers, R.7
Vandenberghe, R.8
Dermaut, B.9
Martin, J.J.10
-
23
-
-
77951183978
-
Prion-like disorders: Blurring the divide between transmissibility and infectivity
-
Cushman M, Johnson BS, King OD, Gitler AD, Shorter J. 2010. Prion-like disorders: Blurring the divide between transmissibility and infectivity. J Cell Sci 123: 1191-1201.
-
(2010)
J Cell Sci
, vol.123
, pp. 1191-1201
-
-
Cushman, M.1
Johnson, B.S.2
King, O.D.3
Gitler, A.D.4
Shorter, J.5
-
24
-
-
77952486387
-
Transgenic mice expressing mutant forms of VCP/p97 recapitulate the full spectrum of IBMPFD including degeneration in muscle, brain and bone
-
Custer SK, Neumann M, Lu H, Wright AC, Taylor JP. 2010. Transgenic mice expressing mutant forms of VCP/p97 recapitulate the full spectrum of IBMPFD including degeneration in muscle, brain and bone. Hum Mol Genet 19: 1741-1755.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 1741-1755
-
-
Custer, S.K.1
Neumann, M.2
Lu, H.3
Wright, A.C.4
Taylor, J.P.5
-
25
-
-
0000999962
-
Un cas de surdité verbale pure terminée par aphasie sensorielle, suivi d'autopsie
-
Déjerine J, Sérieux P. 1897. Un cas de surdité verbale pure terminée par aphasie sensorielle, suivi d'autopsie. CR Acad Sci Paris 49: 1074-1077.
-
(1897)
CR Acad Sci Paris
, vol.49
, pp. 1074-1077
-
-
Déjerine, J.1
Sérieux, P.2
-
26
-
-
80054832080
-
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
-
doi: 10. 1016/j. neuron.09.2011.011
-
DeJesus-Hernandez M, Mackenzie IR, Boeve BF, Boxer AL, Baker M, RutherfordNJ, Nicholson AM, Finch NA, Flynn H, Adamson J, et al. 2011. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron doi: 10. 1016/j. neuron. 2011. 09. 011.
-
(2011)
Neuron
-
-
DeJesus-Hernandez, M.1
McKenzie, I.R.2
Boeve, B.F.3
Boxer, A.L.4
Baker, M.5
Rutherford, N.J.6
Nicholson, A.M.7
Finch, N.A.8
Flynn, H.9
Adamson, J.10
-
27
-
-
77955792022
-
ALS-associated fused in sarcoma (FUS) mutations disrupt transportin-mediated nuclear import
-
Dormann D, Rodde R, Edbauer D, Bentmann E, Fischer I, Hruscha A, Than ME, Mackenzie IRA, Capell A, Schmid B, et al. 2010. ALS-associated fused in sarcoma (FUS) mutations disrupt transportin-mediated nuclear import. EMBO J 29: 21841-21857.
-
(2010)
EMBO J
, vol.29
, pp. 21841-21857
-
-
Dormann, D.1
Rodde, R.2
Edbauer, D.3
Bentmann, E.4
Fischer, I.5
Hruscha, A.6
Than, M.E.7
McKenzie, I.R.A.8
Capell, A.9
Schmid, B.10
-
28
-
-
77952029838
-
New approaches to the pathology and genetics of neurodegeneration
-
Feany MB. 2010. New approaches to the pathology and genetics of neurodegeneration. Am J Pathol 176: 2058-2066.
-
(2010)
Am J Pathol
, vol.176
, pp. 2058-2066
-
-
Feany, M.B.1
-
29
-
-
0029062956
-
Widespread cytoskeletal pathology characterizes corticobasal degeneration
-
Feany MB, Dickson DW. 1995. Widespread cytoskeletal pathology characterizes corticobasal degeneration. Am J Pathol 146: 1388-1396.
-
(1995)
Am J Pathol
, vol.146
, pp. 1388-1396
-
-
Feany, M.B.1
Dickson, D.W.2
-
30
-
-
0030977392
-
Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference
-
Foster NL, Wilhelmsen K, Sima AA, Jones MZ, D'Amato CJ, Gilman S. 1997. Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference. Ann Neurol 41: 706-715.
-
(1997)
Ann Neurol
, vol.41
, pp. 706-715
-
-
Foster, N.L.1
Wilhelmsen, K.2
Sima, A.A.3
Jones, M.Z.4
D'Amato, C.J.5
Gilman, S.6
-
32
-
-
67649273927
-
Propagation of tau misfolding from the outside to the inside of a cell
-
Frost B, Jacks RL, Diamond MI. 2009. Propagation of tau misfolding from the outside to the inside of a cell. J Biol Chem 284: 12845-12852.
-
(2009)
J Biol Chem
, vol.284
, pp. 12845-12852
-
-
Frost, B.1
Jacks, R.L.2
Diamond, M.I.3
-
33
-
-
77953873695
-
Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: A distinct neuropathological and biochemical disease entity
-
Fu YJ, Nishihara Y, Kuroda S, Toyoshima Y, Ishihara T, Shinozaki M, MiyashitaA, Piao YS, Tan CF, Tani T, et al. 2010. Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: A distinct neuropathological and biochemical disease entity. Acta Neuropathol 120: 21-32.
-
(2010)
Acta Neuropathol
, vol.120
, pp. 21-32
-
-
Fu, Y.J.1
Nishihara, Y.2
Kuroda, S.3
Toyoshima, Y.4
Ishihara, T.5
Shinozaki, M.6
Miyashita, A.7
Piao, Y.S.8
Tan, C.F.9
Tani, T.10
-
34
-
-
80054080693
-
White matter damage in primary progressive aphasias: A diffusion tensor tractography study
-
Galantucci S, Tartaglia MC, Wilson SM, Henry ML, Filippi M, Agosta F, DronkersNF, Henry RG, Ogar JM, Miller BL, et al. 2011. White matter damage in primary progressive aphasias: A diffusion tensor tractography study. Brain 134: 3011-3029.
-
(2011)
Brain
, vol.134
, pp. 3011-3029
-
-
Galantucci, S.1
Tartaglia, M.C.2
Wilson, S.M.3
Henry, M.L.4
Filippi, M.5
Agosta, F.6
Dronkers, N.F.7
Henry, R.G.8
Ogar, J.M.9
Miller, B.L.10
-
35
-
-
0033976206
-
Atypical and typical presentations of Alzheimer's disease: A clinical, neuropsychological, neuroimaging and pathological study of 13 cases
-
Galton CJ, Patterson K, Xuereb JH, Hodges JR. 2000. Atypical and typical presentations of Alzheimer's disease: A clinical, neuropsychological, neuroimaging and pathological study of 13 cases. Brain 123: 484-498.
-
(2000)
Brain
, vol.123
, pp. 484-498
-
-
Galton, C.J.1
Patterson, K.2
Xuereb, J.H.3
Hodges, J.R.4
-
36
-
-
0003165598
-
Betrachtungen über Art und Ausbreitung des krankhaften Prozesses in einem Fall von Pickscher Atrophie des Stirnhirns
-
Gans A. 1923. Betrachtungen über Art und Ausbreitung des krankhaften Prozesses in einem Fall von Pickscher Atrophie des Stirnhirns. Z Neurol 80: 10-28.
-
(1923)
Z Neurol
, vol.80
, pp. 10-28
-
-
Gans, A.1
-
37
-
-
0028375988
-
Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles
-
Ghetti B, Tagliavini F, Giaccone G, Bugiani O, Frangione B, Farlow MR, DlouhySR. 1994. Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles. Mol Neurobiol 8: 41-48.
-
(1994)
Mol Neurobiol
, vol.8
, pp. 41-48
-
-
Ghetti, B.1
Tagliavini, F.2
Giaccone, G.3
Bugiani, O.4
Frangione, B.5
Farlow, M.R.6
Dlouhy, S.R.7
-
38
-
-
80855141859
-
Frontotemporal dementia and parkinsonism linked to chromosome 17
-
In, 2nd ed. (ed. Dickson D, Weller RO), Blackwell, Oxford, UK
-
Ghetti B, Wszolek ZW, Boeve BF, Spina S, Goedert M. 2011. Frontotemporal dementia and parkinsonism linked to chromosome 17. In Neurodegeneration: The molecular pathology of dementia and movement disorders, 2nd ed. (ed. Dickson D, Weller RO), pp. 110-134. Blackwell, Oxford, UK.
-
(2011)
Neurodegeneration: The molecular pathology of dementia and movement disorders
, pp. 110-134
-
-
Ghetti, B.1
Wszolek, Z.W.2
Boeve, B.F.3
Spina, S.4
Goedert, M.5
-
39
-
-
54449085260
-
Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration
-
Ghidoni R, Benussi L, Glionna M, Franzoni M, Binetti G. 2008. Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration. Neurology 71: 1235-1239.
-
(2008)
Neurology
, vol.71
, pp. 1235-1239
-
-
Ghidoni, R.1
Benussi, L.2
Glionna, M.3
Franzoni, M.4
Binetti, G.5
-
40
-
-
75949105684
-
TDP-43 redistribution is an early event in sporadic amyotrophic lateral sclerosis
-
Giordana MT, Piccinini M, Grifoni S, De Marco G, Vercellino M, Magistrello M, Pellerino A, Buccinna B, Lupino E, Rinaudo MT. 2010. TDP-43 redistribution is an early event in sporadic amyotrophic lateral sclerosis. Brain Pathol 20: 351-360.
-
(2010)
Brain Pathol
, vol.20
, pp. 351-360
-
-
Giordana, M.T.1
Piccinini, M.2
Grifoni, S.3
De Marco, G.4
Vercellino, M.5
Magistrello, M.6
Pellerino, A.7
Buccinna, B.8
Lupino, E.9
Rinaudo, M.T.10
-
41
-
-
41949119043
-
TDP-43 A315 mutation in familial motor neuron disease
-
Gitcho MA, Baloh RH, Chakraverty S, Mayo K, Norton JB, Levitch D, HatanpaaKJ, White CL, Bigio EH, Caselli R, et al. 2008. TDP-43 A315 mutation in familial motor neuron disease. Ann Neurol 63: 535-538.
-
(2008)
Ann Neurol
, vol.63
, pp. 535-538
-
-
Gitcho, M.A.1
Baloh, R.H.2
Chakraverty, S.3
Mayo, K.4
Norton, J.B.5
Levitch, D.6
Hatanpaa, K.J.7
White, C.L.8
Bigio, E.H.9
Caselli, R.10
-
42
-
-
33750705653
-
A century of Alzheimer's disease
-
Goedert M, Spillantini MG. 2006. A century of Alzheimer's disease. Science 314: 777-781.
-
(2006)
Science
, vol.314
, pp. 777-781
-
-
Goedert, M.1
Spillantini, M.G.2
-
43
-
-
0002792366
-
Cloning and sequencing of the cDNA encoding a core protein of the paired helical filament of Alzheimer disease
-
Goedert M, Wischik CM, Crowther RA, Walker JE, Klug A. 1988. Cloning and sequencing of the cDNA encoding a core protein of the paired helical filament of Alzheimer disease. Proc Natl Acad Sci 85: 4051-4055.
-
(1988)
Proc Natl Acad Sci
, vol.85
, pp. 4051-4055
-
-
Goedert, M.1
Wischik, C.M.2
Crowther, R.A.3
Walker, J.E.4
Klug, A.5
-
44
-
-
0024387161
-
Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated 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. 1989a. Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats: Differential expression of tau protein mRNAs in human brain. EMBO J 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
-
45
-
-
0024745894
-
Multiple isoforms of human microtubule-associated protein tau: Sequences and localization in neurofibrillary tangles of Alzheimer's disease
-
Goedert M, Spillantini MG, Jakes R, Rutherford D, Crowther RA. 1989b. Multiple isoforms of human microtubule-associated protein tau: Sequences and localization in neurofibrillary tangles of Alzheimer's disease. Neuron 3: 519-526.
-
(1989)
Neuron
, vol.3
, pp. 519-526
-
-
Goedert, M.1
Spillantini, M.G.2
Jakes, R.3
Rutherford, D.4
Crowther, R.A.5
-
46
-
-
0026595846
-
Tau proteins of Alzheimer paired helical filaments: Abnormal phosphorylation of all six brain isoforms
-
Goedert M, Spillantini MG, Cairns NJ, Crowther RA. 1992. Tau proteins of Alzheimer paired helical filaments: Abnormal phosphorylation of all six brain isoforms. Neuron 8: 159-168.
-
(1992)
Neuron
, vol.8
, pp. 159-168
-
-
Goedert, M.1
Spillantini, M.G.2
Cairns, N.J.3
Crowther, R.A.4
-
47
-
-
0032919462
-
Effects of frontotemporal dementia FTDP-17 mutations on heparin-induced assembly of tau filaments
-
Goedert M, Jakes R, Crowther RA. 1999. Effects of frontotemporal dementia FTDP-17 mutations on heparin-induced assembly of tau filaments. FEBS Lett 450: 306-311.
-
(1999)
FEBS Lett
, vol.450
, pp. 306-311
-
-
Goedert, M.1
Jakes, R.2
Crowther, R.A.3
-
48
-
-
77954385676
-
The propagation of prion-like protein inclusions in neurodegenerative diseases
-
Goedert M, Clavaguera F, Tolnay M. 2010. The propagation of prion-like protein inclusions in neurodegenerative diseases. Trends Neurosci 33: 317-325.
-
(2010)
Trends Neurosci
, vol.33
, pp. 317-325
-
-
Goedert, M.1
Clavaguera, F.2
Tolnay, M.3
-
49
-
-
12744261481
-
Clinical, cognitive and anatomical evolution from nonfluent progressive aphasia to corticobasal syndrome: A case report
-
Gorno-Tempini ML, Murray RC, Rankin KP, Weiner MW, Miller BL. 2004a. Clinical, cognitive and anatomical evolution from nonfluent progressive aphasia to corticobasal syndrome: a case report. Neurocase 10: 426-436.
-
(2004)
Neurocase
, vol.10
, pp. 426-436
-
-
Gorno-Tempini, M.L.1
Murray, R.C.2
Rankin, K.P.3
Weiner, M.W.4
Miller, B.L.5
-
50
-
-
1442329321
-
Cognition and anatomy in three variants of primary progressive aphasia
-
Gorno-Tempini ML, Dronkers NF, Rankin KP, Ogar JM, Phengrasamy L, RosenHJ, Johnson JK, Weiner MW, Miller BL. 2004b. Cognition and anatomy in three variants of primary progressive aphasia. Ann Neurol 55: 335-346.
-
(2004)
Ann Neurol
, vol.55
, pp. 335-346
-
-
Gorno-Tempini, M.L.1
Dronkers, N.F.2
Rankin, K.P.3
Ogar, J.M.4
Phengrasamy, L.5
Rosen, H.J.6
Johnson, J.K.7
Weiner, M.W.8
Miller, B.L.9
-
51
-
-
54449094214
-
The logopenic/phonological variant of primary progressive aphasia
-
Gorno-Tempini ML, Brambati SM, Ginex V, Ogar J, Dronkers NF, Marcone A, Perani D, Garibotto V, Cappa SF, Miller BL. 2008. The logopenic/phonological variant of primary progressive aphasia. Neurology 71: 1227-1234.
-
(2008)
Neurology
, vol.71
, pp. 1227-1234
-
-
Gorno-Tempini, M.L.1
Brambati, S.M.2
Ginex, V.3
Ogar, J.4
Dronkers, N.F.5
Marcone, A.6
Perani, D.7
Garibotto, V.8
Cappa, S.F.9
Miller, B.L.10
-
52
-
-
79952823979
-
Classification of primary progressive aphasia and its variants
-
Gorno-Tempini ML, Hillis AE, Weintraub S, Kertesz A, Mendez M, Cappa SF, Ogar JM, Rohrer JD, Black S, Boeve BF, et al. 2011. Classification of primary progressive aphasia and its variants. Neurology 76: 1006-1014.
-
(2011)
Neurology
, vol.76
, pp. 1006-1014
-
-
Gorno-Tempini, M.L.1
Hillis, A.E.2
Weintraub, S.3
Kertesz, A.4
Mendez, M.5
Cappa, S.F.6
Ogar, J.M.7
Rohrer, J.D.8
Black, S.9
Boeve, B.F.10
-
53
-
-
0029879720
-
Progressive nonfluent aphasia: Language, cognitive, and PET mesasures contrasted with probable Alzheimer disease
-
Grossman M, Mickanin J, Onishi K, Hughes E, D'Esposito M, Ding XS, Alavi A, Reivich M. 1996. Progressive nonfluent aphasia: Language, cognitive, and PET mesasures contrasted with probable Alzheimer disease. J Cogn Neurosci 8: 135-154.
-
(1996)
J Cogn Neurosci
, vol.8
, pp. 135-154
-
-
Grossman, M.1
Mickanin, J.2
Onishi, K.3
Hughes, E.4
D'Esposito, M.5
Ding, X.S.6
Alavi, A.7
Reivich, M.8
-
54
-
-
0022744803
-
Abnormal phosphorylation of the microtubule-associated protein tau in Alzheimer cytoskeletal pathology
-
Grundke-Iqbal I, Iqbal K, Tung YC, Quinlan M, Wisniewski HM, Binder LI. 1986. Abnormal phosphorylation of the microtubule-associated protein tau in Alzheimer cytoskeletal pathology. Proc Natl Acad Sci 83: 4913-4917.
-
(1986)
Proc Natl Acad Sci
, vol.83
, pp. 4913-4917
-
-
Grundke-Iqbal, I.1
Iqbal, K.2
Tung, Y.C.3
Quinlan, M.4
Wisniewski, H.M.5
Binder, L.I.6
-
55
-
-
11144245270
-
Über ein Brüderpaar mit Pickscher Krankheit
-
Grünthal E. 1930. Über ein Brüderpaar mit Pickscher Krankheit. Z Neurol 129: 350-375.
-
(1930)
Z Neurol
, vol.129
, pp. 350-375
-
-
Grünthal, E.1
-
56
-
-
0023194309
-
Frontal lobe degeneration of non-Alzheimer type. II. Clinical picture and differential diagnosis
-
Gustafson L. 1987. Frontal lobe degeneration of non-Alzheimer type. II. Clinical picture and differential diagnosis. Arch Gerontol Geriatr 6: 209-223.
-
(1987)
Arch Gerontol Geriatr
, vol.6
, pp. 209-223
-
-
Gustafson, L.1
-
57
-
-
65449156394
-
SUT-2 potentiates tau-induced neurotoxity in Caenorhabditis elegans
-
Guthrie CR, Schellenberg GD, Kraemer BC. 2009. SUT-2 potentiates tau-induced neurotoxity in Caenorhabditis elegans. Hum Mol Genet 18: 1825-1838.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 1825-1838
-
-
Guthrie, C.R.1
Schellenberg, G.D.2
Kraemer, B.C.3
-
58
-
-
0037180476
-
Chromosome 3 linked frontotemporal dementia (FTD-3)
-
Gydesen S, Brown JM, Brun A, Chakrabarti L, Gade A, Johannsen P, Rossor M, Thusgaard T, Grove A, Yancopoulou D, et al. 2002. Chromosome 3 linked frontotemporal dementia (FTD-3). Neurology 59: 1585-1594.
-
(2002)
Neurology
, vol.59
, pp. 1585-1594
-
-
Gydesen, S.1
Brown, J.M.2
Brun, A.3
Chakrabarti, L.4
Gade, A.5
Johannsen, P.6
Rossor, M.7
Thusgaard, T.8
Grove, A.9
Yancopoulou, D.10
-
59
-
-
0032561415
-
Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly
-
Hasegawa M, Smith MJ, Goedert M. 1998. Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly. FEBS Lett 437: 207-210.
-
(1998)
FEBS Lett
, vol.437
, pp. 207-210
-
-
Hasegawa, M.1
Smith, M.J.2
Goedert, M.3
-
60
-
-
47949086625
-
Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Hasegawa M, Arai T, Nonaka T, Kametani F, Yoshida M, Hashizume Y, BeachTG, Buratti E, Baralle F, Morita M, et al. 2008. Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Ann Neurol 64: 60-70.
-
(2008)
Ann Neurol
, vol.64
, pp. 60-70
-
-
Hasegawa, M.1
Arai, T.2
Nonaka, T.3
Kametani, F.4
Yoshida, M.5
Hashizume, Y.6
Beach, T.G.7
Buratti, E.8
Baralle, F.9
Morita, M.10
-
61
-
-
35248886083
-
Semantic dementia: A unique clinicopathological syndrome
-
Hodges JR, Patterson K. 2007. Semantic dementia: A unique clinicopathological syndrome. Lancet Neurol 6: 1004-1014.
-
(2007)
Lancet Neurol
, vol.6
, pp. 1004-1014
-
-
Hodges, J.R.1
Patterson, K.2
-
62
-
-
79959689333
-
Common variants affect risk for the tauopathy progressive supranuclear palsy
-
Höglinger GU, Melhem NM, Dickson D, Sleiman PMA, Wang LS, Klei L, Rademakers R, de Silva R, Litvan I, Riley DC, et al. 2011. Common variants affect risk for the tauopathy progressive supranuclear palsy. Nat Genet 43: 699-705.
-
(2011)
Nat Genet
, vol.43
, pp. 699-705
-
-
Höglinger, G.U.1
Melhem, N.M.2
Dickson, D.3
Sleiman, P.M.A.4
Wang, L.S.5
Klei, L.6
Rademakers, R.7
de Silva, R.8
Litvan, I.9
Riley, D.C.10
-
63
-
-
70449517337
-
Absence of FUS-immunoreactive pathology in frontotemporal dementia linked to chromosome 3 (FTD-3) caused by mutation in the CHMP2B gene
-
Holm IE, Isaacs AM, Mackenzie IRA. 2009. Absence of FUS-immunoreactive pathology in frontotemporal dementia linked to chromosome 3 (FTD-3) caused by mutation in the CHMP2B gene. Acta Neuropathol 118: 719-720.
-
(2009)
Acta Neuropathol
, vol.118
, pp. 719-720
-
-
Holm, I.E.1
Isaacs, A.M.2
McKenzie, I.R.A.3
-
64
-
-
78449286213
-
Sortilin-mediated endocytosis determines levels of the frontotemporal dementia protein, progranulin
-
Hu F, Padukkavidana T, Vaegter CB, Brady OA, Zheng Y, Mackenzie IR, FeldmanHH, Nykjaer A, Strittmatter SM. 2010. Sortilin-mediated endocytosis determines levels of the frontotemporal dementia protein, progranulin. Neuron 68: 654-667.
-
(2010)
Neuron
, vol.68
, pp. 654-667
-
-
Hu, F.1
Padukkavidana, T.2
Vaegter, C.B.3
Brady, O.A.4
Zheng, Y.5
McKenzie, I.R.6
Feldman, H.H.7
Nykjaer, A.8
Strittmatter, S.M.9
-
65
-
-
0032543684
-
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
-
Hutton M, Lendon CL, Rizzu M, Baker M, Froelich S, Houlden H, Pickering-Brown S, Chakraverty S, Isaacs A, Grover A, et al. 1998. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 393: 702-705.
-
(1998)
Nature
, vol.393
, pp. 702-705
-
-
Hutton, M.1
Lendon, C.L.2
Rizzu, M.3
Baker, M.4
Froelich, S.5
Houlden, H.6
Pickering-Brown, S.7
Chakraverty, S.8
Isaacs, A.9
Grover, A.10
-
66
-
-
77955322042
-
Dendritic function of tau mediates amyloid-β toxicity in Alzheimer's disease mouse models
-
Ittner LM, Ke YD, Delerue F, Bi M, Gladbach A, Van Eersel J, Wölfing H, ChiengBC, Christie J, Napier IA, et al. 2010. Dendritic function of tau mediates amyloid-β toxicity in Alzheimer's disease mouse models. Cell 142: 387-397.
-
(2010)
Cell
, vol.142
, pp. 387-397
-
-
Ittner, L.M.1
Ke, Y.D.2
Delerue, F.3
Bi, M.4
Gladbach, A.5
Van Eersel, J.6
Wölfing, H.7
Chieng, B.C.8
Christie, J.9
Napier, I.A.10
-
67
-
-
0032850581
-
Clinical and pathological evidence for a frontal variant of Alzheimer disease
-
Johnson JK, Head E, Kim R, Starr A, Cotman CW. 1999. Clinical and pathological evidence for a frontal variant of Alzheimer disease. Arch Neurol 56: 1233-1239.
-
(1999)
Arch Neurol
, vol.56
, pp. 1233-1239
-
-
Johnson, J.K.1
Head, E.2
Kim, R.3
Starr, A.4
Cotman, C.W.5
-
68
-
-
67749133873
-
TDP-43 is intrinsically aggregation-prone, and amyotrophic lateral sclerosis-linked mutations accelerate aggregation and toxicity
-
Johnson BS, Snead D, Lee JJ, McCaffery MM, Shorter J, Gitler AD. 2009. TDP-43 is intrinsically aggregation-prone, and amyotrophic lateral sclerosis-linked mutations accelerate aggregation and toxicity. J Biol Chem 284: 20329-20339.
-
(2009)
J Biol Chem
, vol.284
, pp. 20329-20339
-
-
Johnson, B.S.1
Snead, D.2
Lee, J.J.3
McCaffery, M.M.4
Shorter, J.5
Gitler, A.D.6
-
69
-
-
78649941297
-
Exome sequencing revealsVCP mutations as a cause of familial ALS
-
Johnson JO, Mandrioli J, Benatar M, Abramzon Y, Van Deerlin VM, TrojanowskiJQ, Gibbs JR, Brunetti M, Gronka S, Wuu J, et al. 2010. Exome sequencing revealsVCP mutations as a cause of familial ALS. Neuron 68: 857-864.
-
(2010)
Neuron
, vol.68
, pp. 857-864
-
-
Johnson, J.O.1
Mandrioli, J.2
Benatar, M.3
Abramzon, Y.4
Van Deerlin, V.M.5
Trojanowski, J.Q.6
Gibbs, J.R.7
Brunetti, M.8
Gronka, S.9
Wuu, J.10
-
70
-
-
35848938274
-
Frontotemporal lobar degeneration with upper motor neuron disease/primary lateral sclerosis
-
Josephs KA, Dickson DW. 2007. Frontotemporal lobar degeneration with upper motor neuron disease/primary lateral sclerosis. Neurology 69: 1800-1801.
-
(2007)
Neurology
, vol.69
, pp. 1800-1801
-
-
Josephs, K.A.1
Dickson, D.W.2
-
71
-
-
33745095038
-
Clinicopathological and imaging correlates of progressive aphasia and apraxia of speech
-
Josephs KA, Duffy JR, Strand EA, Whitwell JL, Layton KF, Parisi JE, Hauser MF, Witte RJ, Boeve BF, Knopman DS, et al. 2006. Clinicopathological and imaging correlates of progressive aphasia and apraxia of speech. Brain 129: 1385-1398.
-
(2006)
Brain
, vol.129
, pp. 1385-1398
-
-
Josephs, K.A.1
Duffy, J.R.2
Strand, E.A.3
Whitwell, J.L.4
Layton, K.F.5
Parisi, J.E.6
Hauser, M.F.7
Witte, R.J.8
Boeve, B.F.9
Knopman, D.S.10
-
72
-
-
77953848935
-
Caudate atrophy on MRI is a characteristic feature of FTLD-FUS
-
Josephs KA, Whitwell JL, Parisi JE, Petersen RC, Boeve BF, Jack CR, Dickson DW. 2010. Caudate atrophy on MRI is a characteristic feature of FTLD-FUS. Eur J Neurol 17: 969-975.
-
(2010)
Eur J Neurol
, vol.17
, pp. 969-975
-
-
Josephs, K.A.1
Whitwell, J.L.2
Parisi, J.E.3
Petersen, R.C.4
Boeve, B.F.5
Jack, C.R.6
Dickson, D.W.7
-
73
-
-
77953894192
-
Inclusion body myopathy, Paget's disease of the bone and frontotemporal dementia: A disorder of autophagy
-
Ju JS, Weihl CC. 2010. Inclusion body myopathy, Paget's disease of the bone and frontotemporal dementia: A disorder of autophagy. Hum Mol Genet 19: R38-R45.
-
(2010)
Hum Mol Genet
, vol.19
-
-
Ju, J.S.1
Weihl, C.C.2
-
75
-
-
0034649399
-
The corticobasal degeneration syndrome overlaps progressive aphasia and frontotemporal dementia
-
Kertesz A, Martinez-Lage P, Davidson W, Munoz DG. 2000. The corticobasal degeneration syndrome overlaps progressive aphasia and frontotemporal dementia. Neurology 55: 1368-1375.
-
(2000)
Neurology
, vol.55
, pp. 1368-1375
-
-
Kertesz, A.1
Martinez-Lage, P.2
Davidson, W.3
Munoz, D.G.4
-
76
-
-
33748323156
-
A new chromosome 17q21. 31 microdeletion syndrome associated with a common inversion polymorphism
-
Koolen DA, Vissers LELM, Pfundt R, de Leeuw N, Knight SJL, Regan R, Kooy RF, Reyniers E, Romano C, Fichera M, et al. 2006. A new chromosome 17q21. 31 microdeletion syndrome associated with a common inversion polymorphism. Nat Genet 38: 999-1001.
-
(2006)
Nat Genet
, vol.38
, pp. 999-1001
-
-
Koolen, D.A.1
Vissers, L.E.L.M.2
Pfundt, R.3
de Leeuw, N.4
Knight, S.J.L.5
Regan, R.6
Kooy, R.F.7
Reyniers, E.8
Romano, C.9
Fichera, M.10
-
77
-
-
54449096081
-
White matter tauopathy with globular glial inclusions: A distinct sporadic frontotemporal lobar degeneration
-
Kovacs GG, Majtenyi K, Spina S, Murrell JR, Gelpi E, Höftberger R, Fraser G, Crowther RA, Goedert M, Budka H, et al. 2008. White matter tauopathy with globular glial inclusions: A distinct sporadic frontotemporal lobar degeneration. J Neuropathol Exp Neurol 67: 963-975.
-
(2008)
J Neuropathol Exp Neurol
, vol.67
, pp. 963-975
-
-
Kovacs, G.G.1
Majtenyi, K.2
Spina, S.3
Murrell, J.R.4
Gelpi, E.5
Höftberger, R.6
Fraser, G.7
Crowther, R.A.8
Goedert, M.9
Budka, H.10
-
78
-
-
70350572209
-
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea
-
Kovacs GG, Murrell JR, Horvath S, Haraszti L, Majtenyi K, Molnar MJ, Budka H, Ghetti B, Spina S. 2009. TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea. Mov Disord 24: 1843-1847.
-
(2009)
Mov Disord
, vol.24
, pp. 1843-1847
-
-
Kovacs, G.G.1
Murrell, J.R.2
Horvath, S.3
Haraszti, L.4
Majtenyi, K.5
Molnar, M.J.6
Budka, H.7
Ghetti, B.8
Spina, S.9
-
79
-
-
0042889049
-
Neurodegeneration and defective neurotransmission in aCaenorhabditis elegans model of tauopathy
-
Kraemer BC, Zhang B, Leverenz JB, Thomas JH, Trojanowski JQ, SchellenbergGD. 2003. Neurodegeneration and defective neurotransmission in aCaenorhabditis elegans model of tauopathy. Proc Natl Acad Sci 100: 9980-9985.
-
(2003)
Proc Natl Acad Sci
, vol.100
, pp. 9980-9985
-
-
Kraemer, B.C.1
Zhang, B.2
Leverenz, J.B.3
Thomas, J.H.4
Trojanowski, J.Q.5
Schellenberg, G.D.6
-
80
-
-
61349156118
-
Mutations in the FUS/TLSgene on chromosome 16 cause familial amyotrophic lateral sclerosis
-
Kwiatkowski TJ, Bosco DA, LeClerc AL, Tamrazian E, Vanderburg CR, Russ C, Davis A, Gilchrist J, Kasarskis EJ, Munsat T, et al. 2009. Mutations in the FUS/TLSgene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 323: 1205-1211.
-
(2009)
Science
, vol.323
, pp. 1205-1211
-
-
Kwiatkowski, T.J.1
Bosco, D.A.2
LeClerc, A.L.3
Tamrazian, E.4
Vanderburg, C.R.5
Russ, C.6
Davis, A.7
Gilchrist, J.8
Kasarskis, E.J.9
Munsat, T.10
-
81
-
-
33745449875
-
An inhibitor of tau hyperphosphorylation prevents severe motor impairments in tau transgenic mice
-
Le Corre S, Klafki HW, Plesnila N, Hübinger G, Obermeier A, Sahagún H, MonseB, Seneci P, Lewis J, Eriksen J, et al. 2006. An inhibitor of tau hyperphosphorylation prevents severe motor impairments in tau transgenic mice. Proc Natl Acad Sci 103: 9673-9678.
-
(2006)
Proc Natl Acad Sci
, vol.103
, pp. 9673-9678
-
-
Le Corre, S.1
Klafki, H.W.2
Plesnila, N.3
Hübinger, G.4
Obermeier, A.5
Sahagún, H.6
Monse, B.7
Seneci, P.8
Lewis, J.9
Eriksen, J.10
-
82
-
-
0025904444
-
A68-a major subunit of paired helical filaments and derivatized forms of normal tau
-
Lee VMY, Balin BJ, Otvos L, Trojanowski JQ. 1991. A68-a major subunit of paired helical filaments and derivatized forms of normal tau. Science 251: 675-678.
-
(1991)
Science
, vol.251
, pp. 675-678
-
-
Lee, V.M.Y.1
Balin, B.J.2
Otvos, L.3
Trojanowski, J.Q.4
-
83
-
-
34548492271
-
ESCRT-III dysfunction causes autophagosome accumulation and neurodegeneration
-
Lee JA, Beigneux A, Tariq Ahmad S, Young SG, Gao FB. 2007. ESCRT-III dysfunction causes autophagosome accumulation and neurodegeneration. Curr Biol 17: 1561-1567.
-
(2007)
Curr Biol
, vol.17
, pp. 1561-1567
-
-
Lee, J.A.1
Beigneux, A.2
Tariq Ahmad, S.3
Young, S.G.4
Gao, F.B.5
-
84
-
-
17944382037
-
Enhanced neurofibrillary degeneration in transgenic mice expressing mutant tau and APP
-
Lewis J, Dickson DW, Lin WL, Chisholm L, Corral A, Jones G, Yen SH, Sahara N, Skipper L, Yager D, et al. 2001. Enhanced neurofibrillary degeneration in transgenic mice expressing mutant tau and APP. Science 293: 1487-1491.
-
(2001)
Science
, vol.293
, pp. 1487-1491
-
-
Lewis, J.1
Dickson, D.W.2
Lin, W.L.3
Chisholm, L.4
Corral, A.5
Jones, G.6
Yen, S.H.7
Sahara, N.8
Skipper, L.9
Yager, D.10
-
85
-
-
0025822610
-
Primary progressive aphasia with focal neuronal achromasia
-
Lippa CF, Cohen R, Smith TW, Drachman DA. 1991. Primary progressive aphasia with focal neuronal achromasia. Neurology 41: 882-886.
-
(1991)
Neurology
, vol.41
, pp. 882-886
-
-
Lippa, C.F.1
Cohen, R.2
Smith, T.W.3
Drachman, D.A.4
-
86
-
-
8944226575
-
Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome)
-
Litvan I, Agid Y, Calne D, Campbell G, Dubois B, Duvoisin RC, Goetz CG, GolbeLI, Grafman J, Growdon JH, et al. 1996. Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome). Neurology 47: 1-9.
-
(1996)
Neurology
, vol.47
, pp. 1-9
-
-
Litvan, I.1
Agid, Y.2
Calne, D.3
Campbell, G.4
Dubois, B.5
Duvoisin, R.C.6
Goetz, C.G.7
Golbe, L.I.8
Grafman, J.9
Growdon, J.H.10
-
87
-
-
0001702382
-
Picksche Krankheit
-
In, (ed. Henke F, Lubarsch O), Springer, Berlin
-
Lüers T, Spatz H. 1957. Picksche Krankheit. In Handbuch der speziellen Anatomie und Histologie (ed. Henke F, Lubarsch O), Vol. 13, pp. 614-715. Springer, Berlin.
-
(1957)
Handbuch der speziellen Anatomie und Histologie
, vol.13
, pp. 614-715
-
-
Lüers, T.1
Spatz, H.2
-
88
-
-
33749668518
-
Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration. Classification and relation to clinical phenotype
-
Mackenzie IRA, Baborie A, Pickering-Brown S, Du Plessis D, Jaros E, Perry RH, Neary D, Snowden JS, Mann DMA. 2006. Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration. Classification and relation to clinical phenotype. Acta Neuropathol 112: 539-549.
-
(2006)
Acta Neuropathol
, vol.112
, pp. 539-549
-
-
McKenzie, I.R.A.1
Baborie, A.2
Pickering-Brown, S.3
Du Plessis, D.4
Jaros, E.5
Perry, R.H.6
Neary, D.7
Snowden, J.S.8
Mann, D.M.A.9
-
89
-
-
79959599081
-
A harmonized classification system for FTLD-TDP pathology
-
Mackenzie IRA, Neumann M, Baborie A, Sampathu DM, Du Plessis D, Jaros E, Perry RH, Trojanowski JQ, Mann DMA, Lee VMY. 2011. A harmonized classification system for FTLD-TDP pathology. Acta Neuropathol 122: 111-113.
-
(2011)
Acta Neuropathol
, vol.122
, pp. 111-113
-
-
McKenzie, I.R.A.1
Neumann, M.2
Baborie, A.3
Sampathu, D.M.4
Du Plessis, D.5
Jaros, E.6
Perry, R.H.7
Trojanowski, J.Q.8
Mann, D.M.A.9
Lee, V.M.Y.10
-
90
-
-
0020037788
-
Slowly progressive aphasia without generalized dementia
-
Mesulam MM. 1982. Slowly progressive aphasia without generalized dementia. Ann Neurol 11: 592-598.
-
(1982)
Ann Neurol
, vol.11
, pp. 592-598
-
-
Mesulam, M.M.1
-
91
-
-
0023630829
-
Primary progressive aphasia-differentiation from Alzheimer's disease
-
Mesulam MM. 1987. Primary progressive aphasia-differentiation from Alzheimer's disease. Ann Neurol 22: 533-534.
-
(1987)
Ann Neurol
, vol.22
, pp. 533-534
-
-
Mesulam, M.M.1
-
92
-
-
0035071053
-
Primary progressive aphasia
-
Mesulam MM. 2001. Primary progressive aphasia. Ann Neurol 49: 425-432.
-
(2001)
Ann Neurol
, vol.49
, pp. 425-432
-
-
Mesulam, M.M.1
-
93
-
-
46749090490
-
Alzheimer and frontotemporal pathology in subsets of primary progressive aphasia
-
Mesulam MM, Wicklund A, Johnson N, Rogalski E, Léger GC, Rademaker A, Weintraub S, Bigio EH. 2008. Alzheimer and frontotemporal pathology in subsets of primary progressive aphasia. Ann Neurol 63: 709-719.
-
(2008)
Ann Neurol
, vol.63
, pp. 709-719
-
-
Mesulam, M.M.1
Wicklund, A.2
Johnson, N.3
Rogalski, E.4
Léger, G.C.5
Rademaker, A.6
Weintraub, S.7
Bigio, E.H.8
-
94
-
-
0000417917
-
Über eine der amyotrophischen Lateralsklerose nahestehende Erkrankung mit psychischen Störungen
-
Meyer A. 1929. Über eine der amyotrophischen Lateralsklerose nahestehende Erkrankung mit psychischen Störungen. Z Neurol 121: 107-128.
-
(1929)
Z Neurol
, vol.121
, pp. 107-128
-
-
Meyer, A.1
-
95
-
-
72049128028
-
Clinical syndromes associated with posterior atrophy
-
Migliaccio R, Agosta F, Rascovsky K, Karydas A, Bonasera S, Rabinovici GD, Miller BL, Gorno-Tempini ML. 2009. Clinical syndromes associated with posterior atrophy. Neurology 73: 1571-1578.
-
(2009)
Neurology
, vol.73
, pp. 1571-1578
-
-
Migliaccio, R.1
Agosta, F.2
Rascovsky, K.3
Karydas, A.4
Bonasera, S.5
Rabinovici, G.D.6
Miller, B.L.7
Gorno-Tempini, M.L.8
-
96
-
-
0023229520
-
Presenile dementia combined with amyotrophy: A review of 34 Japanese cases
-
Morita K, Kaiya H, Ikeda T, Namba M. 1987. Presenile dementia combined with amyotrophy: A review of 34 Japanese cases. Arch Gerontol Geriatr 6: 263-277.
-
(1987)
Arch Gerontol Geriatr
, vol.6
, pp. 263-277
-
-
Morita, K.1
Kaiya, H.2
Ikeda, T.3
Namba, M.4
-
98
-
-
0032935471
-
Disrupted temporal lobe connections in semantic dementia
-
Mummery CJ, Patterson K, Wise RJS, Vandenberghe R, Price CJ, Hodges JR. 1999. Disrupted temporal lobe connections in semantic dementia. Brain 122: 61-73.
-
(1999)
Brain
, vol.122
, pp. 61-73
-
-
Mummery, C.J.1
Patterson, K.2
Wise, R.J.S.3
Vandenberghe, R.4
Price, C.J.5
Hodges, J.R.6
-
99
-
-
70449517359
-
FUS pathology in basophilic inclusion body disease
-
Munoz DG, Neumann M, Kusaka H, Yokota O, Ishihara K, Terada S, Kuroda S, Mackenzie IR. 2009. FUS pathology in basophilic inclusion body disease. Acta Neuropathol 118: 617-627.
-
(2009)
Acta Neuropathol
, vol.118
, pp. 617-627
-
-
Munoz, D.G.1
Neumann, M.2
Kusaka, H.3
Yokota, O.4
Ishihara, K.5
Terada, S.6
Kuroda, S.7
McKenzie, I.R.8
-
100
-
-
0032763203
-
Tau gene mutation G389R causes a tauopathy with abundant Pick body-like inclusions and axonal deposits
-
Murrell JR, Spillantini MG, Zolo P, Guazzelli M, Smith MJ, Hasegawa M, Redi F, Crowther RA, Pietrini P, Ghetti B, et al. 1999. Tau gene mutation G389R causes a tauopathy with abundant Pick body-like inclusions and axonal deposits. J Neuropathol Exp Neurol 58: 1207-1226.
-
(1999)
J Neuropathol Exp Neurol
, vol.58
, pp. 1207-1226
-
-
Murrell, J.R.1
Spillantini, M.G.2
Zolo, P.3
Guazzelli, M.4
Smith, M.J.5
Hasegawa, M.6
Redi, F.7
Crowther, R.A.8
Pietrini, P.9
Ghetti, B.10
-
101
-
-
0033011181
-
Accelerated filament formation from tau protein with specific FTDP-17 mutations
-
Nacharaju P, Lewis J, Easson C, Yen S, Hackett J, Hutton M, Yen SH. 1999. Accelerated filament formation from tau protein with specific FTDP-17 mutations. FEBS Lett 447: 195-199.
-
(1999)
FEBS Lett
, vol.447
, pp. 195-199
-
-
Nacharaju, P.1
Lewis, J.2
Easson, C.3
Yen, S.4
Hackett, J.5
Hutton, M.6
Yen, S.H.7
-
103
-
-
0142153171
-
Progressive non-fluent aphasia is associated with hypometabolism centred on the left anterior insula
-
Neary D, Snowden JS, Gustafson L, Passant U, Stuss D, Black S, Freedman M, Kertesz A, Robert PH, Albert M, et al. 2003. Progressive non-fluent aphasia is associated with hypometabolism centred on the left anterior insula. Brain 126: 2406-2418.
-
(2003)
Brain
, vol.126
, pp. 2406-2418
-
-
Neary, D.1
Snowden, J.S.2
Gustafson, L.3
Passant, U.4
Stuss, D.5
Black, S.6
Freedman, M.7
Kertesz, A.8
Robert, P.H.9
Albert, M.10
-
104
-
-
0142153171
-
Progressive non-fluent aphasia is associated with hypometabolism centred on the left anterior insula
-
Nestor PJ, Graham NL, Fryer TD, Williams GB, Patterson K, Hodges JR. 2003. Progressive non-fluent aphasia is associated with hypometabolism centred on the left anterior insula. Brain 126: 2406-2418.
-
(2003)
Brain
, vol.126
, pp. 2406-2418
-
-
Nestor, P.J.1
Graham, N.L.2
Fryer, T.D.3
Williams, G.B.4
Patterson, K.5
Hodges, J.R.6
-
105
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, Chou TT, Bruce J, Schuck T, Grossman M, Clark CM, et al. 2006. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314: 130-133.
-
(2006)
Science
, vol.314
, pp. 130-133
-
-
Neumann, M.1
Sampathu, D.M.2
Kwong, L.K.3
Truax, A.C.4
Micsenyi, M.C.5
Chou, T.T.6
Bruce, J.7
Schuck, T.8
Grossman, M.9
Clark, C.M.10
-
106
-
-
33846815066
-
TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations
-
Neumann M, Mackenzie IR, Cairns NJ, Boyer PJ, Markesbery WR, Smith CD, Taylor JP, Kretzschmar HA, Kimonis VE, Forman MS. 2007. TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations. J Neuropathol Exp Neurol 66: 152-157.
-
(2007)
J Neuropathol Exp Neurol
, vol.66
, pp. 152-157
-
-
Neumann, M.1
McKenzie, I.R.2
Cairns, N.J.3
Boyer, P.J.4
Markesbery, W.R.5
Smith, C.D.6
Taylor, J.P.7
Kretzschmar, H.A.8
Kimonis, V.E.9
Forman, M.S.10
-
107
-
-
70350673956
-
A new subtype of frontotemporal lobar degeneration with FUS pathology
-
Neumann M, Rademakers R, Roeber S, Baker M, Kretzschmar HA, MackenzieIRA. 2009a. A new subtype of frontotemporal lobar degeneration with FUS pathology. Brain 132: 2922-2931.
-
(2009)
Brain
, vol.132
, pp. 2922-2931
-
-
Neumann, M.1
Rademakers, R.2
Roeber, S.3
Baker, M.4
Kretzschmar, H.A.5
McKenzie, I.R.A.6
-
108
-
-
70449521091
-
Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease
-
Neumann A, Roeber S, Kretzschmar HA, Rademakers R, Baker M, MackenzieIRA. 2009b. Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease. Acta Neuropathol 118: 605-616.
-
(2009)
Acta Neuropathol
, vol.118
, pp. 605-616
-
-
Neumann, A.1
Roeber, S.2
Kretzschmar, H.A.3
Rademakers, R.4
Baker, M.5
McKenzie, I.R.A.6
-
109
-
-
73649148708
-
Characterization of alternative isoforms and inclusion body of the TAR DNA-binding protein-43
-
Nishimoto Y, Ito D, Yagi T, Nihei Y, Tsunoda Y, Suzuki N. 2010. Characterization of alternative isoforms and inclusion body of the TAR DNA-binding protein-43. J Biol Chem 285: 608-619.
-
(2010)
J Biol Chem
, vol.285
, pp. 608-619
-
-
Nishimoto, Y.1
Ito, D.2
Yagi, T.3
Nihei, Y.4
Tsunoda, Y.5
Suzuki, N.6
-
110
-
-
0025814639
-
New ubiquitin-positive intraneuronal inclusions in the extra-motor cortices in patients with amyotrophic lateral sclerosis
-
Okamoto K, Hirai S, Yamazaki T, Sun X, Nakazato Y. 1991. New ubiquitin-positive intraneuronal inclusions in the extra-motor cortices in patients with amyotrophic lateral sclerosis. Neurosci Lett 129: 233-236.
-
(1991)
Neurosci Lett
, vol.129
, pp. 233-236
-
-
Okamoto, K.1
Hirai, S.2
Yamazaki, T.3
Sun, X.4
Nakazato, Y.5
-
111
-
-
0000952928
-
Anatomische Beiträge zur Lehre von der Pickschen umschriebenen Grosshirnrinden-Atrophie ("Picksche Krankheit")
-
Onari K, Spatz H. 1926. Anatomische Beiträge zur Lehre von der Pickschen umschriebenen Grosshirnrinden-Atrophie ("Picksche Krankheit"). Z Neurol 101: 470-511.
-
(1926)
Z Neurol
, vol.101
, pp. 470-511
-
-
Onari, K.1
Spatz, H.2
-
112
-
-
0033951680
-
Significant association between the tau gene A0/A0 genotype and Parkinson's disease
-
Pastor P, Ezquerra M, Munoz E, Marti MJ, Blesa R, Tolosa E, Oliva R. 2000. Significant association between the tau gene A0/A0 genotype and Parkinson's disease. Ann Neurol 47: 242-245.
-
(2000)
Ann Neurol
, vol.47
, pp. 242-245
-
-
Pastor, P.1
Ezquerra, M.2
Munoz, E.3
Marti, M.J.4
Blesa, R.5
Tolosa, E.6
Oliva, R.7
-
113
-
-
0000244405
-
Ueber die Beziehungen der senilen Hirnatrophie zur Aphasie
-
Pick A. 1892. Ueber die Beziehungen der senilen Hirnatrophie zur Aphasie. Prager med Wschr 17: 165-167.
-
(1892)
Prager med Wschr
, vol.17
, pp. 165-167
-
-
Pick, A.1
-
114
-
-
0000665886
-
Senile Hirnatrophie als Grundlage von Herderscheinungen
-
Pick A. 1901. Senile Hirnatrophie als Grundlage von Herderscheinungen. Wiener klin Wschr 14: 403-404.
-
(1901)
Wiener klin Wschr
, vol.14
, pp. 403-404
-
-
Pick, A.1
-
115
-
-
84941014963
-
Zur Symptomatologie der linksseitigen Schläfenlappenatrophie
-
Pick A. 1904. Zur Symptomatologie der linksseitigen Schläfenlappenatrophie. Mschr Psychiat Neurol 16: 378-388.
-
(1904)
Mschr Psychiat Neurol
, vol.16
, pp. 378-388
-
-
Pick, A.1
-
116
-
-
84940806954
-
Über einen weiteren Symptomencomplex im Rahmen der Dementia senilis, bedingt durch umschriebene stärkere Hirnatrophie (gemischte Apraxie)
-
Pick A. 1906. Über einen weiteren Symptomencomplex im Rahmen der Dementia senilis, bedingt durch umschriebene stärkere Hirnatrophie (gemischte Apraxie). Mschr Psychiat Neurol 19: 97-108.
-
(1906)
Mschr Psychiat Neurol
, vol.19
, pp. 97-108
-
-
Pick, A.1
-
117
-
-
13544251748
-
Anthraquinones inhibit tau aggregation and dissolve Alzheimer paired helical filaments in vitro and in cells
-
Pickhardt M, Gazova Z, von Bergen M, Khlistunova I, Wang Y, Hascher A, Mandelkow EM, Biernat J, Mandelkow E. 2005. Anthraquinones inhibit tau aggregation and dissolve Alzheimer paired helical filaments in vitro and in cells. J Biol Chem 280: 3628-3635.
-
(2005)
J Biol Chem
, vol.280
, pp. 3628-3635
-
-
Pickhardt, M.1
Gazova, Z.2
von Bergen, M.3
Khlistunova, I.4
Wang, Y.5
Hascher, A.6
Mandelkow, E.M.7
Biernat, J.8
Mandelkow, E.9
-
118
-
-
78751579187
-
Behavioural-variant frontotemporal dementia: Diagnosis, clinical staging, and management
-
Piguet O, Hornberger M, Mioshi E, Hodges JR. 2011a. Behavioural-variant frontotemporal dementia: Diagnosis, clinical staging, and management. Lancet Neurol 10: 162-172.
-
(2011)
Lancet Neurol
, vol.10
, pp. 162-172
-
-
Piguet, O.1
Hornberger, M.2
Mioshi, E.3
Hodges, J.R.4
-
119
-
-
78751633939
-
Clinical phenotypes in autopsy-confirmed Pick disease
-
Piguet O, Halliday GW, Reid WGJ, Casey B, Carman R, Huang Y, Xuereb JH, Hodges JR, Kril JJ. 2011b. Clinical phenotypes in autopsy-confirmed Pick disease. Neurology 76: 253-259.
-
(2011)
Neurology
, vol.76
, pp. 253-259
-
-
Piguet, O.1
Halliday, G.W.2
Reid, W.G.J.3
Casey, B.4
Carman, R.5
Huang, Y.6
Xuereb, J.H.7
Hodges, J.R.8
Kril, J.J.9
-
120
-
-
0022976136
-
Filamentous aggregates in Pick's disease, progressive supranuclear palsy, and Alzheimer's disease share antigenic determinants with microtubule-associated protein, tau
-
Pollock NJ, Mirra SS, Binder LI, Hansen LA, Wood JG. 1986. Filamentous aggregates in Pick's disease, progressive supranuclear palsy, and Alzheimer's disease share antigenic determinants with microtubule-associated protein, tau. Lancet 328: 1211.
-
(1986)
Lancet
, vol.328
, pp. 1211
-
-
Pollock, N.J.1
Mirra, S.S.2
Binder, L.I.3
Hansen, L.A.4
Wood, J.G.5
-
121
-
-
79953185674
-
Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43
-
Polymenidou M, Lagier-Tourenne C, Hutt KR, Huelga SC, Moran J, Liang TY, Ling SC, Sun E, Wancewicz E, Mazur C, et al. 2011. Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43. Nat Neurosci 14: 459-468.
-
(2011)
Nat Neurosci
, vol.14
, pp. 459-468
-
-
Polymenidou, M.1
Lagier-Tourenne, C.2
Hutt, K.R.3
Huelga, S.C.4
Moran, J.5
Liang, T.Y.6
Ling, S.C.7
Sun, E.8
Wancewicz, E.9
Mazur, C.10
-
122
-
-
14444284106
-
Tau is a candidate gene for chromosome 17 frontotemporal dementia
-
Poorkaj P, Bird TD, Wijsman E, Nemens E, Garruto RM, Anderson L, AndreadisA, Wiederholt WC, Raskind M, Schellenberg GD. 1998. Tau is a candidate gene for chromosome 17 frontotemporal dementia. Ann Neurol 43: 815-825.
-
(1998)
Ann Neurol
, vol.43
, pp. 815-825
-
-
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
-
123
-
-
55849121534
-
Aβ amyloid and glucose metabolism in three variants of primary progressive aphasia
-
Rabinovici GD, Jagust WJ, Furst AJ, Ogar JM, Racine CA, Mormino EC, O'Neil JP, Lal RA, Dronkers NF, Miller BL, et al. 2008. Aβ amyloid and glucose metabolism in three variants of primary progressive aphasia. Ann Neurol 64: 388-401.
-
(2008)
Ann Neurol
, vol.64
, pp. 388-401
-
-
Rabinovici, G.D.1
Jagust, W.J.2
Furst, A.J.3
Ogar, J.M.4
Racine, C.A.5
Mormino, E.C.6
O'Neil, J.P.7
Lal, R.A.8
Dronkers, N.F.9
Miller, B.L.10
-
124
-
-
0014225976
-
Corticodentonigral degeneration with neuronal achromasia
-
Rebeiz JJ, Kolodny EM, Richardson EP. 1968. Corticodentonigral degeneration with neuronal achromasia. Arch Neurol 18: 20-33.
-
(1968)
Arch Neurol
, vol.18
, pp. 20-33
-
-
Rebeiz, J.J.1
Kolodny, E.M.2
Richardson, E.P.3
-
125
-
-
0030826625
-
Autosomal dominant dementia with widespread neurofibrillary tangles
-
Reed LA, Grabowski TJ, Schmidt ML, Morris JC, Goate A, Solodkin A, Van Hoesen GW, Schelper RL, Talbot CJ, Wragg MA, et al. 1997. Autosomal dominant dementia with widespread neurofibrillary tangles. Ann Neurol 42: 564-572.
-
(1997)
Ann Neurol
, vol.42
, pp. 564-572
-
-
Reed, L.A.1
Grabowski, T.J.2
Schmidt, M.L.3
Morris, J.C.4
Goate, A.5
Solodkin, A.6
Van Hoesen, G.W.7
Schelper, R.L.8
Talbot, C.J.9
Wragg, M.A.10
-
126
-
-
80054837386
-
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
-
doi: 10. 1016/j. neuron.09.2011.010
-
Renton AE, Majounie E, Waite A, Simón-Sanchez J, Rollinson S, Gibbs JR, Schymick JC, Laaksovirta H, Van Swieten JC, Myllykangas L, et al. 2011. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron doi: 10. 1016/j. neuron. 2011. 09. 010.
-
(2011)
Neuron
-
-
Renton, A.E.1
Majounie, E.2
Waite, A.3
Simón-Sanchez, J.4
Rollinson, S.5
Gibbs, J.R.6
Schymick, J.C.7
Laaksovirta, H.8
Van Swieten, J.C.9
Myllykangas, L.10
-
127
-
-
0010565997
-
Eine besondere Art von Stirnhirnschwund mit Verblödung
-
Richter H. 1918. Eine besondere Art von Stirnhirnschwund mit Verblödung. Z Neurol 38: 127-159.
-
(1918)
Z Neurol
, vol.38
, pp. 127-159
-
-
Richter, H.1
-
128
-
-
77953194507
-
TDP-43 mediates degeneration in a novel Drosophila model of disease caused by mutations in VCP/p97
-
Ritson GP, Custer SK, Freibaum BD, Guinto JB, Geffel D, Moore J, Tang W, Winton MJ, Neumann M, Trojanowski JQ, et al. 2010. TDP-43 mediates degeneration in a novel Drosophila model of disease caused by mutations in VCP/p97. J Neurosci 30: 7729-7739.
-
(2010)
J Neurosci
, vol.30
, pp. 7729-7739
-
-
Ritson, G.P.1
Custer, S.K.2
Freibaum, B.D.3
Guinto, J.B.4
Geffel, D.5
Moore, J.6
Tang, W.7
Winton, M.J.8
Neumann, M.9
Trojanowski, J.Q.10
-
129
-
-
34248181511
-
Reducing endogenous tau ameliorates amyloid β-induced deficits in an Alzheimer's disease mouse model
-
Roberson ED, Scearce-Levie K, Palop JJ, Yan F, Cheng IH, Wu T, Gerstein H, YuGQ, Mucke L. 2007. Reducing endogenous tau ameliorates amyloid β-induced deficits in an Alzheimer's disease mouse model. Science 316: 750-754.
-
(2007)
Science
, vol.316
, pp. 750-754
-
-
Roberson, E.D.1
Scearce-Levie, K.2
Palop, J.J.3
Yan, F.4
Cheng, I.H.5
Wu, T.6
Gerstein, H.7
Yu, G.Q.8
Mucke, L.9
-
130
-
-
77955312709
-
The diagnosis of young-onset dementia
-
Rossor MN, Fox NC, Mummery CM, Schott JM, Warren JD. 2010. The diagnosis of young-onset dementia. Lancet Neurol 9, 793-806.
-
(2010)
Lancet Neurol
, vol.9
, pp. 793-806
-
-
Rossor, M.N.1
Fox, N.C.2
Mummery, C.M.3
Schott, J.M.4
Warren, J.D.5
-
131
-
-
33846076379
-
Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies
-
Sampathu DM, Neumann M, Kwong LK, Chou TT, Micsenyi M, Truax A, Bruce J, Grossman M, Trojanowski JQ, Lee VMY. 2006. Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies. Am J Pathol 169: 1343-1352.
-
(2006)
Am J Pathol
, vol.169
, pp. 1343-1352
-
-
Sampathu, D.M.1
Neumann, M.2
Kwong, L.K.3
Chou, T.T.4
Micsenyi, M.5
Truax, A.6
Bruce, J.7
Grossman, M.8
Trojanowski, J.Q.9
Lee, V.M.Y.10
-
132
-
-
79952167224
-
Prion propagation and toxicity in vivo occur in two distinct mechanistic phases
-
Sandberg MK, Al-Doujaily H, Sharps B, Clarke AR, Collinge J. 2011. Prion propagation and toxicity in vivo occur in two distinct mechanistic phases. Nature 470: 540-542.
-
(2011)
Nature
, vol.470
, pp. 540-542
-
-
Sandberg, M.K.1
Al-Doujaily, H.2
Sharps, B.3
Clarke, A.R.4
Collinge, J.5
-
133
-
-
22344438508
-
Tau suppression in a neurodegenerative mouse model improves memory function
-
Santacruz K, Lewis J, Spires T, Paulson J, KKKotilinek L, Ingelsson M, GuimaresA, DeTure M, Ramsden M, McGowan E, et al. 2005. Tau suppression in a neurodegenerative mouse model improves memory function. Science 309: 476-481.
-
(2005)
Science
, vol.309
, pp. 476-481
-
-
Santacruz, K.1
Lewis, J.2
Spires, T.3
Paulson, J.4
Kotilinek, K.K.L.5
Ingelsson, M.6
Guimares, A.7
DeTure, M.8
Ramsden, M.9
McGowan, E.10
-
134
-
-
27644469489
-
Mutation of Vps54causes motor neuron disease and defective spermiogenesis in the wobbler mouse
-
Schmitt-John T, Drepper C, Mussmann A, Hahn P, Kuhlmann M, Thiel C, Hafner M, Lengeling A, Heimann P, Jones JM, et al. 2005. Mutation of Vps54causes motor neuron disease and defective spermiogenesis in the wobbler mouse. Nat Genet 37: 1213-1215.
-
(2005)
Nat Genet
, vol.37
, pp. 1213-1215
-
-
Schmitt-John, T.1
Drepper, C.2
Mussmann, A.3
Hahn, P.4
Kuhlmann, M.5
Thiel, C.6
Hafner, M.7
Lengeling, A.8
Heimann, P.9
Jones, J.M.10
-
135
-
-
0000745129
-
Über Picksche Krankheit
-
Schneider C. 1927. Über Picksche Krankheit. Mschr Psychiat Neurol 65: 230-275.
-
(1927)
Mschr Psychiat Neurol
, vol.65
, pp. 230-275
-
-
Schneider, C.1
-
136
-
-
0009851414
-
Weitere Beiträge zur Lehre von der Pickschen Krankheit
-
Schneider C. 1929. Weitere Beiträge zur Lehre von der Pickschen Krankheit. Z Neurol 120: 340-384.
-
(1929)
Z Neurol
, vol.120
, pp. 340-384
-
-
Schneider, C.1
-
137
-
-
77954459337
-
Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration
-
Seelaar H, Klijnsma KY, de Koning I, Van der Lugt A, Chiu WZ, Azmani A, Rozemuller AJM, Van Swieten JC. 2010. Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration. J Neurol 257: 747-753.
-
(2010)
J Neurol
, vol.257
, pp. 747-753
-
-
Seelaar, H.1
Klijnsma, K.Y.2
de Koning, I.3
Van der Lugt, A.4
Chiu, W.Z.5
Azmani, A.6
Rozemuller, A.J.M.7
Van Swieten, J.C.8
-
138
-
-
33748333194
-
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome
-
Sharp AJ, Hansen S, Selzer RR, Cheng Z, Regan R, Hurst JA, Stewart H, Price SM, Blair E, Hennekam RC, et al. 2006. Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome. Nat Genet 38: 1038-1042.
-
(2006)
Nat Genet
, vol.38
, pp. 1038-1042
-
-
Sharp, A.J.1
Hansen, S.2
Selzer, R.R.3
Cheng, Z.4
Regan, R.5
Hurst, J.A.6
Stewart, H.7
Price, S.M.8
Blair, E.9
Hennekam, R.C.10
-
139
-
-
78649918873
-
Capturing VCP: Another molecular piece in the ALS jigsaw puzzle
-
Shaw CE. 2010. Capturing VCP: Another molecular piece in the ALS jigsaw puzzle. Neuron 68: 812-814.
-
(2010)
Neuron
, vol.68
, pp. 812-814
-
-
Shaw, C.E.1
-
140
-
-
33748300645
-
Microdeletion encompassingMAPT at chromosome 17q21. 3 is associated with developmental delay and learning disability
-
Shaw-Smith C, Pittman AM, Willatt L, Martin H, Rickman L, Gribble S, Curley R, Cumming S, Dunn C, Kalaitzopoulos D, et al. 2006. Microdeletion encompassingMAPT at chromosome 17q21. 3 is associated with developmental delay and learning disability. Nat Genet 38: 1032-1037.
-
(2006)
Nat Genet
, vol.38
, pp. 1032-1037
-
-
Shaw-Smith, C.1
Pittman, A.M.2
Willatt, L.3
Martin, H.4
Rickman, L.5
Gribble, S.6
Curley, R.7
Cumming, S.8
Dunn, C.9
Kalaitzopoulos, D.10
-
141
-
-
23044471011
-
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
-
Skibinski G, Parkinson NJ, Brown JM, Charkrabarti L, Lloyd SL, Hummerich H, Nielsen JE, Hodges JR, Spillantini MG, Thusgaard T, et al. 2005. Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia. Nat Genet 37: 806-808.
-
(2005)
Nat Genet
, vol.37
, pp. 806-808
-
-
Skibinski, G.1
Parkinson, N.J.2
Brown, J.M.3
Charkrabarti, L.4
Lloyd, S.L.5
Hummerich, H.6
Nielsen, J.E.7
Hodges, J.R.8
Spillantini, M.G.9
Thusgaard, T.10
-
142
-
-
0000021167
-
Semantic dementia: A form of circumscribed atrophy
-
Snowden JS, Goulding PJ, Neary D. 1989. Semantic dementia: A form of circumscribed atrophy. Behav Neurol 2: 167-182.
-
(1989)
Behav Neurol
, vol.2
, pp. 167-182
-
-
Snowden, J.S.1
Goulding, P.J.2
Neary, D.3
-
143
-
-
0030000867
-
Comparison of the neurofibrillary pathology in Alzheimer's disease and familial presenile dementia with tangles
-
Spillantini MG, Crowther RA, Goedert M. 1996. Comparison of the neurofibrillary pathology in Alzheimer's disease and familial presenile dementia with tangles. Acta Neuropathol 92: 42-48.
-
(1996)
Acta Neuropathol
, vol.92
, pp. 42-48
-
-
Spillantini, M.G.1
Crowther, R.A.2
Goedert, M.3
-
144
-
-
0030887854
-
Familial multiple system tauopathy with presenile dementia: A disease with abundant neuronal and glial tau filaments
-
Spillantini MG, Goedert M, Crowther RA, Murrell JR, Farlow MR, Ghetti B. 1997. Familial multiple system tauopathy with presenile dementia: A disease with abundant neuronal and glial tau filaments. Proc Natl Acad Sci 94: 4113-4118.
-
(1997)
Proc Natl Acad Sci
, vol.94
, pp. 4113-4118
-
-
Spillantini, M.G.1
Goedert, M.2
Crowther, R.A.3
Murrell, J.R.4
Farlow, M.R.5
Ghetti, B.6
-
145
-
-
0031949084
-
Frontotemporal dementia and parkinsonism linked to chromosome 17: A new group of tauopathies
-
Spillantini MG, Bird TD, Ghetti B. 1998a. Frontotemporal dementia and parkinsonism linked to chromosome 17: A new group of tauopathies. Brain Pathol 8: 387-402.
-
(1998)
Brain Pathol
, vol.8
, pp. 387-402
-
-
Spillantini, M.G.1
Bird, T.D.2
Ghetti, B.3
-
146
-
-
0032560487
-
Mutation in the tau gene in familial multiple system tauopathy with presenile dementia
-
Spillantini MG, Murrell JR, Goedert M, Farlow MR, Klug A, Ghetti B. 1998b. Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. Proc Natl Acad Sci 95: 7737-7741.
-
(1998)
Proc Natl Acad Sci
, 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
-
147
-
-
0031738468
-
Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau
-
Spillantini MG, Crowther RA, Kamphorst W, Heutink P, Van Swieten JC. 1998c. Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau. Am J Pathol 153: 1359-1363.
-
(1998)
Am J Pathol
, vol.153
, pp. 1359-1363
-
-
Spillantini, M.G.1
Crowther, R.A.2
Kamphorst, W.3
Heutink, P.4
Van Swieten, J.C.5
-
148
-
-
34948898536
-
Corticobasal syndrome associated with the A90D progranulin mutation
-
Spina S, Murrell JR, Huey ED, Wassermann EM, Pietrini P, Grafman J, Ghetti B. 2007. Corticobasal syndrome associated with the A90D progranulin mutation. J Neuropathol Exp Neurol 66: 892-900.
-
(2007)
J Neuropathol Exp Neurol
, vol.66
, pp. 892-900
-
-
Spina, S.1
Murrell, J.R.2
Huey, E.D.3
Wassermann, E.M.4
Pietrini, P.5
Grafman, J.6
Ghetti, B.7
-
149
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
Sreedharan J, Blair IP, Tripathi VB, Hu X, Vance C, Rogelj B, Ackerley S, DurnallJC, Williams KL, Buratti E, et al. 2008. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 319: 1668-1672.
-
(2008)
Science
, vol.319
, pp. 1668-1672
-
-
Sreedharan, J.1
Blair, I.P.2
Tripathi, V.B.3
Hu, X.4
Vance, C.5
Rogelj, B.6
Ackerley, S.7
Durnall, J.C.8
Williams, K.L.9
Buratti, E.10
-
150
-
-
13944278863
-
A common inversion under selection in Europeans
-
Stefansson H, Helgason A, Thorleifsson, Steintorsdottir V, Masson G, BarnardJ, Baker A, Jonasdottir A, Ingason A, Gudnadottir VG, et al. 2005. A common inversion under selection in Europeans. Nat Genet 37: 129-137.
-
(2005)
Nat Genet
, vol.37
, pp. 129-137
-
-
Stefansson, H.1
Helgason, A.2
Thorleifsson, S.V.3
Masson, G.4
Barnard, J.5
Baker, A.6
Jonasdottir, A.7
Ingason, A.8
Gudnadottir, V.G.9
-
152
-
-
33847188685
-
Über die Picksche Atrophie
-
Stertz G. 1926. Über die Picksche Atrophie. Z Neurol 101: 729-749.
-
(1926)
Z Neurol
, vol.101
, pp. 729-749
-
-
Stertz, G.1
-
154
-
-
79955502687
-
Molecular determinants and genetic modifiers of aggregation and toxicity for the ALS disease protein FUS/TLS
-
Sun Z, Diaz Z, Fang X, Hart MP, Chesi A, Shorter J, Gitler AD. 2011. Molecular determinants and genetic modifiers of aggregation and toxicity for the ALS disease protein FUS/TLS. PLoS Biol 9: e1000614.
-
(2011)
PLoS Biol
, vol.9
-
-
Sun, Z.1
Diaz, Z.2
Fang, X.3
Hart, M.P.4
Chesi, A.5
Shorter, J.6
Gitler, A.D.7
-
155
-
-
79955477738
-
The growth factor progranulin binds to TNF receptors and is therapeutic against inflammatory arthritis in mice
-
Tang W, Lu Y, Tian QY, Zhang Y, Guo FJ, Liu GY, Syed NM, Lai Y, Lin EA, KongL, et al. 2011. The growth factor progranulin binds to TNF receptors and is therapeutic against inflammatory arthritis in mice. Science 332: 478-484.
-
(2011)
Science
, vol.332
, pp. 478-484
-
-
Tang, W.1
Lu, Y.2
Tian, Q.Y.3
Zhang, Y.4
Guo, F.J.5
Liu, G.Y.6
Syed, N.M.7
Lai, Y.8
Lin, E.A.9
Kong, L.10
-
156
-
-
14844303721
-
Inhibition of heparin-induced tau filament formation by phenothiazines, polyphenols and porphyrins
-
Taniguchi S, Suzuki N, Masuda M, Hisanaga SI, Iwatsubo T, Goedert M, Hasegawa M. 2005. Inhibition of heparin-induced tau filament formation by phenothiazines, polyphenols and porphyrins. J Biol Chem 280: 7614-7623.
-
(2005)
J Biol Chem
, vol.280
, pp. 7614-7623
-
-
Taniguchi, S.1
Suzuki, N.2
Masuda, M.3
Hisanaga, S.I.4
Iwatsubo, T.5
Goedert, M.6
Hasegawa, M.7
-
157
-
-
70350156915
-
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort
-
Ticozzi N, Silani V, LeClerc AL, Keagle P, Gellera C, Ratti A, Taroni F, Kwiatkowski TJ, McKenna-Yasek DN, Sapp PC, et al. 2009. Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort. Neurology 73: 1180-1185.
-
(2009)
Neurology
, vol.73
, pp. 1180-1185
-
-
Ticozzi, N.1
Silani, V.2
LeClerc, A.L.3
Keagle, P.4
Gellera, C.5
Ratti, A.6
Taroni, F.7
Kwiatkowski, T.J.8
McKenna-Yasek, D.N.9
Sapp, P.C.10
-
158
-
-
79953180492
-
Characterizing the RNA targets and position-dependent splicing regulation by TDP-43
-
Tollervey JR, Curk T, Rogelj B, Riese M, Cereda M, Kayikci M, König J, Hortobágyi T, Nishimura AL, Zupunski V, et al. 2011. Characterizing the RNA targets and position-dependent splicing regulation by TDP-43. Nat Neurosci 14: 452-458.
-
(2011)
Nat Neurosci
, vol.14
, pp. 452-458
-
-
Tollervey, J.R.1
Curk, T.2
Rogelj, B.3
Riese, M.4
Cereda, M.5
Kayikci, M.6
König, J.7
Hortobágyi, T.8
Nishimura, A.L.9
Zupunski, V.10
-
159
-
-
33645069660
-
Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13. p2-21. 3
-
Vance C, Al-Chalabi A, Ruddy D, Smith BN, Hu X, Sreedharan J, Siddique T, Schelhaas HJ, Kusters B, Troost D, et al. 2006. Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13. p2-21. 3. Brain 129: 868-876.
-
(2006)
Brain
, vol.129
, pp. 868-876
-
-
Vance, C.1
Al-Chalabi, A.2
Ruddy, D.3
Smith, B.N.4
Hu, X.5
Sreedharan, J.6
Siddique, T.7
Schelhaas, H.J.8
Kusters, B.9
Troost, D.10
-
160
-
-
61349162349
-
Mutations in FUS, an RNA processing protein, cause familial amyotrophic sclerosis type 6
-
Vance C, Rogelj B, Hortobágyi T, De Vos KJ, Nihimura AL, Sreedharan J, Hu X, Smith B, Ruddy D, Wright P, et al. 2009. Mutations in FUS, an RNA processing protein, cause familial amyotrophic sclerosis type 6. Science 323: 1208-1211.
-
(2009)
Science
, vol.323
, pp. 1208-1211
-
-
Vance, C.1
Rogelj, B.2
Hortobágyi, T.3
De Vos, K.J.4
Nihimura, A.L.5
Sreedharan, J.6
Hu, X.7
Smith, B.8
Ruddy, D.9
Wright, P.10
-
161
-
-
77649136250
-
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
-
Van Deerlin VM, Sleiman PMA, Martinez-Lage M, Chen-Plotkin A, Wang LS, Graff-Radford NR, Dickson DW, Rademakers R, Boeve BF, Grossman M, et al. 2010. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nat Genet 42: 234-239.
-
(2010)
Nat Genet
, vol.42
, pp. 234-239
-
-
Van Deerlin, V.M.1
Sleiman, P.M.A.2
Martinez-Lage, M.3
Chen-Plotkin, A.4
Wang, L.S.5
Graff-Radford, N.R.6
Dickson, D.W.7
Rademakers, R.8
Boeve, B.F.9
Grossman, M.10
-
162
-
-
79951722994
-
Early-onset versus late-onset Alzheimer's disease: The case of the missing APOE ε4 allele
-
Van der Flier WM, Pijnenburg YAL, Fox NC, Scheltens P. 2011. Early-onset versus late-onset Alzheimer's disease: The case of the missing APOE ε4 allele. Lancet Neurol 10: 280-288.
-
(2011)
Lancet Neurol
, vol.10
, pp. 280-288
-
-
Van der Flier, W.M.1
Pijnenburg, Y.A.L.2
Fox, N.C.3
Scheltens, P.4
-
164
-
-
51449089054
-
Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia
-
Van Swieten JC, Heutink P. 2008. Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia. Lancet Neurol 7: 965-974.
-
(2008)
Lancet Neurol
, vol.7
, pp. 965-974
-
-
Van Swieten, J.C.1
Heutink, P.2
-
166
-
-
3843069669
-
Neurodegeneration caused by proteins with an aberrant carboxyl-terminus
-
Vidal R, Delisle MB, Ghetti B. 2004. Neurodegeneration caused by proteins with an aberrant carboxyl-terminus. J Neuropathol Exp Neurol 63: 787-800.
-
(2004)
J Neuropathol Exp Neurol
, vol.63
, pp. 787-800
-
-
Vidal, R.1
Delisle, M.B.2
Ghetti, B.3
-
167
-
-
0001741444
-
Picksche Krankheit und amyotrophische Lateralsklerose
-
Von Braunmühl A. 1932. Picksche Krankheit und amyotrophische Lateralsklerose. Allg Z Psychiat 96: 364-366.
-
(1932)
Allg Z Psychiat
, vol.96
, pp. 364-366
-
-
Von Braunmühl, A.1
-
168
-
-
0006500103
-
Über ein Schwesternpaar mit Pickscher Krankheit
-
Von Braunmühl A, Leonhard K. 1934. Über ein Schwesternpaar mit Pickscher Krankheit. Z Neurol 150: 209-241.
-
(1934)
Z Neurol
, vol.150
, pp. 209-241
-
-
Von Braunmühl, A.1
Leonhard, K.2
-
169
-
-
1842483843
-
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
-
Watts GDJ, Wymer J, Kovach MJ, Mehta SG, Mumm S, Darvish D, Pestronk A, Whyte MP, Kimonis VE. 2004. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. Nat Genet 36: 377-381.
-
(2004)
Nat Genet
, vol.36
, pp. 377-381
-
-
Watts, G.D.J.1
Wymer, J.2
Kovach, M.J.3
Mehta, S.G.4
Mumm, S.5
Darvish, D.6
Pestronk, A.7
Whyte, M.P.8
Kimonis, V.E.9
-
171
-
-
50849110525
-
p73 regulates neurodegeneration and phospho-tau accumulation in aging and Alzheimer's disease
-
Wetzel MK, Naska S, Laliberte CL, Rymar VV, Fujitani M, Biernaskie JA, Cole CJ, Lerch JP, Spring S, Wang SH, et al. 2008. p73 regulates neurodegeneration and phospho-tau accumulation in aging and Alzheimer's disease. Neuron 59: 708-721.
-
(2008)
Neuron
, vol.59
, pp. 708-721
-
-
Wetzel, M.K.1
Naska, S.2
Laliberte, C.L.3
Rymar, V.V.4
Fujitani, M.5
Biernaskie, J.A.6
Cole, C.J.7
Lerch, J.P.8
Spring, S.9
Wang, S.H.10
-
172
-
-
33645828452
-
Patterns of atrophy in pathologically confirmed FTLD with and without motor neuron degeneration
-
Whitwell JL, Jack CR, Senjem ML, Josephs KA. 2006. Patterns of atrophy in pathologically confirmed FTLD with and without motor neuron degeneration. Neurology 66: 102-104.
-
(2006)
Neurology
, vol.66
, pp. 102-104
-
-
Whitwell, J.L.1
Jack, C.R.2
Senjem, M.L.3
Josephs, K.A.4
-
173
-
-
70350683356
-
Distinct anatomical subtypes of the behavioural variant of frontotemporal dementia: A cluster analysis study
-
Whitwell JL, Przybelski SA, Weigand SD, Ivnik RJ, Vemuri P, Gunter JL, SenjemML, Shiung MM, Boeve BF, Knopman DS, et al. 2009a. Distinct anatomical subtypes of the behavioural variant of frontotemporal dementia: A cluster analysis study. Brain 132: 2932-2946.
-
(2009)
Brain
, vol.132
, pp. 2932-2946
-
-
Whitwell, J.L.1
Przybelski, S.A.2
Weigand, S.D.3
Ivnik, R.J.4
Vemuri, P.5
Gunter, J.L.6
Senjem, M.L.7
Shiung, M.M.8
Boeve, B.F.9
Knopman, D.S.10
-
174
-
-
62849095858
-
Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN
-
Whitwell JL, Jack CR, Boeve BF, Senjem ML, Baker M, Rademakers R, Ivnik RJ, Knopman DS, Wszolek ZK, Petersen RC, et al. 2009b. Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN. Neurology 72: 813-820.
-
(2009)
Neurology
, vol.72
, pp. 813-820
-
-
Whitwell, J.L.1
Jack, C.R.2
Boeve, B.F.3
Senjem, M.L.4
Baker, M.5
Rademakers, R.6
Ivnik, R.J.7
Knopman, D.S.8
Wszolek, Z.K.9
Petersen, R.C.10
-
175
-
-
77951465425
-
Gray and white matter water diffusion in the syndromic variants of frontotemporal dementia
-
Whitwell JL, Avula R, Senjem ML, Kantarci K, Weigand SD, Samikoglu A, Edmonson HA, Vemuri P, Knopman DS, Boeve BF, et al. 2010a. Gray and white matter water diffusion in the syndromic variants of frontotemporal dementia. Neurology 74: 1279-1287.
-
(2010)
Neurology
, vol.74
, pp. 1279-1287
-
-
Whitwell, J.L.1
Avula, R.2
Senjem, M.L.3
Kantarci, K.4
Weigand, S.D.5
Samikoglu, A.6
Edmonson, H.A.7
Vemuri, P.8
Knopman, D.S.9
Boeve, B.F.10
-
176
-
-
78649994826
-
Imaging correlates of pathology in corticobasal syndrome
-
Whitwell JL, Jack CR, Boeve BF, Parisi JE, Ahlskog JE, Drubach DA, Senjem ML, Knopman DS, Petersen RC, Dickson DW, et al. 2010b. Imaging correlates of pathology in corticobasal syndrome. Neurology 75: 1879-1887.
-
(2010)
Neurology
, vol.75
, pp. 1879-1887
-
-
Whitwell, J.L.1
Jack, C.R.2
Boeve, B.F.3
Parisi, J.E.4
Ahlskog, J.E.5
Drubach, D.A.6
Senjem, M.L.7
Knopman, D.S.8
Petersen, R.C.9
Dickson, D.W.10
-
177
-
-
0028073692
-
Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22
-
Wilhelmsen KC, Lynch T, Pavlou E, Higgins M, Nygaard TG. 1994. Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22. Am J Hum Genet 55: 1159-1164.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 1159-1164
-
-
Wilhelmsen, K.C.1
Lynch, T.2
Pavlou, E.3
Higgins, M.4
Nygaard, T.G.5
-
178
-
-
60249088182
-
Progressive supranuclear palsy: Clinicopathological concepts and diagnostic challenges
-
Williams DR, Lees AJ. 2009. Progressive supranuclear palsy: Clinicopathological concepts and diagnostic challenges. Lancet Neurol 8: 270-279.
-
(2009)
Lancet Neurol
, vol.8
, pp. 270-279
-
-
Williams, D.R.1
Lees, A.J.2
-
179
-
-
34250865548
-
Pathological tau burden and distribution distinguishes progressive supranuclear palsy-parkinsonism from Richardson's syndrome
-
Williams DR, Holton JL, Strand C, Pittman A, de Silva R, Lees AJ, Revesz T. 2007. Pathological tau burden and distribution distinguishes progressive supranuclear palsy-parkinsonism from Richardson's syndrome. Brain 130: 1566-1576.
-
(2007)
Brain
, vol.130
, pp. 1566-1576
-
-
Williams, D.R.1
Holton, J.L.2
Strand, C.3
Pittman, A.4
de Silva, R.5
Lees, A.J.6
Revesz, T.7
-
180
-
-
0003986552
-
Isolation of a fragment of tau derived from the core of the paired helical filament of Alzheimer disease
-
Wischik CM, Novak M, Thogersen HC, Edwards PC, Runswick MJ, Jakes R, Walker JE, Milstein C, Roth M, Klug A. 1988. Isolation of a fragment of tau derived from the core of the paired helical filament of Alzheimer disease. Proc Natl Acad Sci 85: 4506-4510.
-
(1988)
Proc Natl Acad Sci
, vol.85
, pp. 4506-4510
-
-
Wischik, C.M.1
Novak, M.2
Thogersen, H.C.3
Edwards, P.C.4
Runswick, M.J.5
Jakes, R.6
Walker, J.E.7
Milstein, C.8
Roth, M.9
Klug, A.10
-
181
-
-
0035958642
-
Tauopathy in Drosophila: Neurodegeneration without neurofibrillary tangles
-
Wittmann CW, Wszolek ZF, Shulman JM, Salvaterra PM, Lewis J, Hutton M, Feany MB. 2001. Tauopathy in Drosophila: Neurodegeneration without neurofibrillary tangles. Science 293: 711-714.
-
(2001)
Science
, vol.293
, pp. 711-714
-
-
Wittmann, C.W.1
Wszolek, Z.F.2
Shulman, J.M.3
Salvaterra, P.M.4
Lewis, J.5
Hutton, M.6
Feany, M.B.7
-
182
-
-
42949094584
-
TDP-43 mutation in familial amyotrophic lateral sclerosis
-
Yokoseki A, Shiga A, Tan CF, Tagawa A, Kaneko H, Koyama A, Eguchi H, Tsujino A, Ikeuchi T, Kakita A, et al. 2008. TDP-43 mutation in familial amyotrophic lateral sclerosis. Ann Neurol 63: 538-542.
-
(2008)
Ann Neurol
, vol.63
, pp. 538-542
-
-
Yokoseki, A.1
Shiga, A.2
Tan, C.F.3
Tagawa, A.4
Kaneko, H.5
Koyama, A.6
Eguchi, H.7
Tsujino, A.8
Ikeuchi, T.9
Kakita, A.10
-
183
-
-
76149123541
-
The spectrum of mutations in progranulin
-
Yu CE, Bird TD, Bekris LM, Montine TJ, Leverenz JB, Steinbart E, Galloway NM, Feldman H, Woltjer R, Miller CA, et al. 2010. The spectrum of mutations in progranulin. Arch Neurol 67: 161-170.
-
(2010)
Arch Neurol
, vol.67
, pp. 161-170
-
-
Yu, C.E.1
Bird, T.D.2
Bekris, L.M.3
Montine, T.J.4
Leverenz, J.B.5
Steinbart, E.6
Galloway, N.M.7
Feldman, H.8
Woltjer, R.9
Miller, C.A.10
-
184
-
-
77951921512
-
Divergent network connectivity changes in behavioural variant frontotemporal dementia and Alzheimer's disease
-
Zhou J, Greicius MD, Gennatas ED, Growdon ME, Jang JY, Rabinovici GD, Kramer JH, Weiner M, Miller BL, Seeley WW. 2010. Divergent network connectivity changes in behavioural variant frontotemporal dementia and Alzheimer's disease. Brain 133: 1352-1367.
-
(2010)
Brain
, vol.133
, pp. 1352-1367
-
-
Zhou, J.1
Greicius, M.D.2
Gennatas, E.D.3
Growdon, M.E.4
Jang, J.Y.5
Rabinovici, G.D.6
Kramer, J.H.7
Weiner, M.8
Miller, B.L.9
Seeley, W.W.10
|