-
1
-
-
34249949338
-
TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease
-
Amador-Ortiz C, Lin WL, Ahmed Z, Personett D, Davies P, Duara R, et al. TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease. Ann Neurol 2007; 61: 435-45.
-
(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
-
2
-
-
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, et al. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem Biophys Res Commun 2006; 351: 602-11.
-
(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
-
3
-
-
0038509194
-
Frontotemporal and motor neurone degeneration with neurofilament inclusion bodies: Additional evidence for overlap between FTD and ALS
-
Bigio EH, Lipton AM, White CL, Dickson DW, Hirano A. Frontotemporal and motor neurone degeneration with neurofilament inclusion bodies: additional evidence for overlap between FTD and ALS. Neuropathol Appl Neurobiol 2003; 29: 239-53.
-
(2003)
Neuropathol Appl Neurobiol
, vol.29
, pp. 239-253
-
-
Bigio, E.H.1
Lipton, A.M.2
White, C.L.3
Dickson, D.W.4
Hirano, A.5
-
4
-
-
0038609639
-
Epidemiology and genetics of frontotemporal dementia/Pick's disease
-
Bird T, Knopman D, Van Swieten J, Rosso S, Feldman H, Tanabe H, et al. Epidemiology and genetics of frontotemporal dementia/Pick's disease. Ann Neurol 2003; 54 (Suppl 5): S29-31.
-
(2003)
Ann Neurol
, vol.54
, Issue.SUPPL. 5
-
-
Bird, T.1
Knopman, D.2
Van Swieten, J.3
Rosso, S.4
Feldman, H.5
Tanabe, H.6
-
5
-
-
0035794665
-
Nuclear factor TDP-43 and SP proteins promote in vitro and in vivo CFTR exon skipping
-
Buratti E, Dork T, Zuccato E, Pagani F, Romano M, Baralle FE. Nuclear factor TDP-43 and SP proteins promote in vitro and in vivo CFTR exon skipping. EMBO J 2001; 20: 1774-84.
-
(2001)
EMBO J
, vol.20
, pp. 1774-1784
-
-
Buratti, E.1
Dork, T.2
Zuccato, E.3
Pagani, F.4
Romano, M.5
Baralle, F.E.6
-
6
-
-
34447096691
-
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: Consensus of the Consortium for Frontotemporal Lobar Degeneration
-
Cairns NJ, Bigio EH, Mackenzie IRA, Neumann M, Lee VMY, Hatanpaa KJ, et al. Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration. Acta Neuropathol 2007a; 114: 5-22.
-
(2007)
Acta Neuropathol
, vol.114
, pp. 5-22
-
-
Cairns, N.J.1
Bigio, E.H.2
Mackenzie, I.R.A.3
Neumann, M.4
Lee, V.M.Y.5
Hatanpaa, K.J.6
-
7
-
-
7044262166
-
Clinical and neuropathological variation in neuronal intermediate filament inclusion disease
-
Cairns NJ, Grossman M, Arnold SE, Burn DJ, Jaros E, Perry RH, et al. Clinical and neuropathological variation in neuronal intermediate filament inclusion disease. Neurology 2004; 26: 1376-84.
-
(2004)
Neurology
, vol.26
, pp. 1376-1384
-
-
Cairns, N.J.1
Grossman, M.2
Arnold, S.E.3
Burn, D.J.4
Jaros, E.5
Perry, R.H.6
-
8
-
-
34547663747
-
TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions
-
Cairns NJ, Neumann M, Bigio EH, Holm IE, Troost D, Hatanpaa KJ, et al. TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions. Am J Pathol 2007b; 171: 227-40.
-
(2007)
Am J Pathol
, vol.171
, pp. 227-240
-
-
Cairns, N.J.1
Neumann, M.2
Bigio, E.H.3
Holm, I.E.4
Troost, D.5
Hatanpaa, K.J.6
-
10
-
-
34247625005
-
Neary Ubiquitinated pathological, lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43
-
Davidson Y, Kelley T, Mackenzie IRA, Pickering-Brown S, Du Plessis D, Neary D, et al. Neary Ubiquitinated pathological, lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43. Acta Neuropathol 2007; 113: 521-33.
-
(2007)
Acta Neuropathol
, vol.113
, pp. 521-533
-
-
Davidson, Y.1
Kelley, T.2
Mackenzie, I.R.A.3
Pickering-Brown, S.4
Du Plessis, D.5
Neary, D.6
-
11
-
-
0043163673
-
A Canadian cohort study of cognitive impairment and related dementias (ACCORD): Study methods and baseline results
-
Feldman H, Levy AR, Hsiung GY, Peters KR, Donald A, Black SE, et al. A Canadian cohort study of cognitive impairment and related dementias (ACCORD): study methods and baseline results. Neuroepidemiology 2003; 22: 265-74.
-
(2003)
Neuroepidemiology
, vol.22
, pp. 265-274
-
-
Feldman, H.1
Levy, A.R.2
Hsiung, G.Y.3
Peters, K.R.4
Donald, A.5
Black, S.E.6
-
12
-
-
33746693220
-
Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations
-
Forman MS, Mackenzie IR, Cairns NJ, Swanson E, Boyer PJ, Drachman DA, et al. Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations. J Neuopathol Exp Neurol 2006; 65: 571-81.
-
(2006)
J Neuopathol Exp Neurol
, vol.65
, pp. 571-581
-
-
Forman, M.S.1
Mackenzie, I.R.2
Cairns, N.J.3
Swanson, E.4
Boyer, P.J.5
Drachman, D.A.6
-
14
-
-
37549059158
-
TAR-DNA binding protein 43 in Pick disease
-
Freeman SH, Spires-Jones T, Hyman BT, Growdon JH, Frosch MP. TAR-DNA binding protein 43 in Pick disease. J Neuropathol Exp Neurol 2008; 67: 62-7.
-
(2008)
J Neuropathol Exp Neurol
, vol.67
, pp. 62-67
-
-
Freeman, S.H.1
Spires-Jones, T.2
Hyman, B.T.3
Growdon, J.H.4
Frosch, M.P.5
-
15
-
-
36949036676
-
Pathological TDP-43 in parkinsonism-dementia complex and amyotrophic lateral sclerosis of Guam
-
Geser F, Winton MJ, Kwong LK, Xu Y, Xie SX, Igaz LM, et al. Pathological TDP-43 in parkinsonism-dementia complex and amyotrophic lateral sclerosis of Guam. Acta Neuropathol 2008; 115: 133-45.
-
(2008)
Acta Neuropathol
, vol.115
, pp. 133-145
-
-
Geser, F.1
Winton, M.J.2
Kwong, L.K.3
Xu, Y.4
Xie, S.X.5
Igaz, L.M.6
-
16
-
-
0037180476
-
Chromosome 3 linked frontotemporal dementia (FTD-3)
-
Gydesen S, Brown JM, Brun A, Chakrabarti L, Gade A, Johannsen P, et al. Chromosome 3 linked frontotemporal dementia (FTD-3). Neurology 2002; 59: 1585-94.
-
(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
-
17
-
-
0028887661
-
Dementia with ALS features and diffuse Pick body-like inclusions (atypical Pick's disease?)
-
Hamada K, Fukazawa T, Yanagihara T, Yoshida K, Hamada T, Yoshimura N, et al. Dementia with ALS features and diffuse Pick body-like inclusions (atypical Pick's disease?). Clin Neuropathol 1995; 14: 1-6.
-
(1995)
Clin Neuropathol
, vol.14
, pp. 1-6
-
-
Hamada, K.1
Fukazawa, T.2
Yanagihara, T.3
Yoshida, K.4
Hamada, T.5
Yoshimura, N.6
-
18
-
-
36348972414
-
Concurrence of TDP-43, tau and α-synuclein pathology in brains of Alzheimer's disease and dementia with Lewy bodies
-
Higashi S, Iseki E, Yamamoto R, Minegishi M, Hino H, Fujisawa K, et al. Concurrence of TDP-43, tau and α-synuclein pathology in brains of Alzheimer's disease and dementia with Lewy bodies. Brain Res 2007; 1184: 284-94.
-
(2007)
Brain Res
, vol.1184
, pp. 284-294
-
-
Higashi, S.1
Iseki, E.2
Yamamoto, R.3
Minegishi, M.4
Hino, H.5
Fujisawa, K.6
-
19
-
-
34948838317
-
A Reassessment of the Neuropathology of Frontotemporal Dementia Linked to Chromosome 3 (FTD-3)
-
Holm IE, Englund E, Mackenzie IRA, Johannsen P, Isaacs A. A Reassessment of the Neuropathology of Frontotemporal Dementia Linked to Chromosome 3 (FTD-3). J Neuropathol Exp Neurol 2007; 66: 884-91.
-
(2007)
J Neuropathol Exp Neurol
, vol.66
, pp. 884-891
-
-
Holm, I.E.1
Englund, E.2
Mackenzie, I.R.A.3
Johannsen, P.4
Isaacs, A.5
-
20
-
-
33749030182
-
An autopsy case of frontotemporal dementia with sever dysarthria and motor neuron disease showing numerous basophilic inclusions
-
Ishihara K, Araki S, Ihori N, Shiota JI, Kawamura M, Nakano I. An autopsy case of frontotemporal dementia with sever dysarthria and motor neuron disease showing numerous basophilic inclusions. Neuropathology 2006; 26: 447-54.
-
(2006)
Neuropathology
, vol.26
, pp. 447-454
-
-
Ishihara, K.1
Araki, S.2
Ihori, N.3
Shiota, J.I.4
Kawamura, M.5
Nakano, I.6
-
22
-
-
20844443269
-
Frontotemporal lobar degeneration. Demographic characteristics of 353 patients
-
Johnson JK, Diehl J, Mendez MF, Neuhaus J, Shapira JS, Forman M, et al. Frontotemporal lobar degeneration. Demographic characteristics of 353 patients. Arch Neurol 2005; 62: 925-30.
-
(2005)
Arch Neurol
, vol.62
, pp. 925-930
-
-
Johnson, J.K.1
Diehl, J.2
Mendez, M.F.3
Neuhaus, J.4
Shapira, J.S.5
Forman, M.6
-
23
-
-
0242336433
-
Neurofilament inclusion body disease: A new proteinopathy?
-
Josephs KA, Holton JL, Rossor MN, Braendgaard H, Ozawa T, Fox NC, et al. Neurofilament inclusion body disease: a new proteinopathy? Brain 2003; 126: 2291-303.
-
(2003)
Brain
, vol.126
, pp. 2291-2303
-
-
Josephs, K.A.1
Holton, J.L.2
Rossor, M.N.3
Braendgaard, H.4
Ozawa, T.5
Fox, N.C.6
-
24
-
-
4344642855
-
Frontotemporal lobar degeneration and ubiquitin immunohistochemistry
-
Jospehs KA, Holton JL, Rossor MN, Godbolt AK, Ozawa T, Strand K, et al. Frontotemporal lobar degeneration and ubiquitin immunohistochemistry. Neuropathol Appl Neurobiol 2004; 30: 369-73.
-
(2004)
Neuropathol Appl Neurobiol
, vol.30
, pp. 369-373
-
-
Jospehs, K.A.1
Holton, J.L.2
Rossor, M.N.3
Godbolt, A.K.4
Ozawa, T.5
Strand, K.6
-
25
-
-
33645642025
-
Ubiquitin immunohistochemistry of frontotemporal lobar degeneration differentiates cases with and without motor neuron disease
-
Katsuse O, Dickson DW. Ubiquitin immunohistochemistry of frontotemporal lobar degeneration differentiates cases with and without motor neuron disease. Alz Dis Assoc Disord 2005; 19 (Suppl 1): S37-43.
-
(2005)
Alz Dis Assoc Disord
, vol.19
, Issue.SUPPL. 1
-
-
Katsuse, O.1
Dickson, D.W.2
-
26
-
-
0027184764
-
Adult-onset motor neuron disease with basophilic intraneuronal inclusion bodies
-
Kusaka H, Matsumoto S, Imai T. Adult-onset motor neuron disease with basophilic intraneuronal inclusion bodies. Clin Neuropathol 1993; 12: 215-8.
-
(1993)
Clin Neuropathol
, vol.12
, pp. 215-218
-
-
Kusaka, H.1
Matsumoto, S.2
Imai, T.3
-
27
-
-
34447103093
-
TDP-43 proteinopathy: A neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease
-
Kwong LK, Neumann M, Sampathu DM, Lee VMY, Trojanowski JQ. TDP-43 proteinopathy: a neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease. Act Neuropathol 2007; 114: 63-70.
-
(2007)
Act Neuropathol
, vol.114
, pp. 63-70
-
-
Kwong, L.K.1
Neumann, M.2
Sampathu, D.M.3
Lee, V.M.Y.4
Trojanowski, J.Q.5
-
28
-
-
0037044240
-
The overlap of amyotrophic lateral sclerosis and frontotemporal dementia
-
Lomen-Hoerth C, Anderson T, Miller B. The overlap of amyotrophic lateral sclerosis and frontotemporal dementia. Neurology 2002; 59: 1077-9.
-
(2002)
Neurology
, vol.59
, pp. 1077-1079
-
-
Lomen-Hoerth, C.1
Anderson, T.2
Miller, B.3
-
29
-
-
0000993417
-
The Lund & Manchester Groups. Consensus statement. Clinical and neuropathological criteria for fronto-temporal dementia
-
The Lund & Manchester Groups. Consensus statement. Clinical and neuropathological criteria for fronto-temporal dementia. J Neurosurg Neurol Psychiatry 1994; 4: 416-8.
-
(1994)
J Neurosurg Neurol Psychiatry
, vol.4
, pp. 416-418
-
-
-
30
-
-
33749668518
-
Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: Classification and relation to clinical phenotype
-
Mackenzie IRA, Baborie A, Pickering-Brown S, du Pleissis D, Jaros E, Perry RH, et al. Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype. Acta Neuropathol 2006a; 112: 539-49.
-
(2006)
Acta Neuropathol
, vol.112
, pp. 539-549
-
-
Mackenzie, I.R.A.1
Baborie, A.2
Pickering-Brown, S.3
du Pleissis, D.4
Jaros, E.5
Perry, R.H.6
-
31
-
-
33750590113
-
The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene
-
Mackenzie IRA, Baker M, Pickering-Brown S, Hsiung GYR, Lindholm C, Dwosh E, et al. The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene. Brain 2006b; 129: 3081-90.
-
(2006)
Brain
, vol.129
, pp. 3081-3090
-
-
Mackenzie, I.R.A.1
Baker, M.2
Pickering-Brown, S.3
Hsiung, G.Y.R.4
Lindholm, C.5
Dwosh, E.6
-
32
-
-
34249946466
-
Pathological TDP-43 distinguishes sporadic ALS from ALS with SOD-1 mutations
-
Mackenzie IRA, Bigio EH, Ince PG, Geser F, Neumann M, Cairns NJ, et al. Pathological TDP-43 distinguishes sporadic ALS from ALS with SOD-1 mutations. Ann Neurol 2007; 61: 427-34.
-
(2007)
Ann Neurol
, vol.61
, pp. 427-434
-
-
Mackenzie, I.R.A.1
Bigio, E.H.2
Ince, P.G.3
Geser, F.4
Neumann, M.5
Cairns, N.J.6
-
33
-
-
3343019026
-
Neurofilament inclusion body disease with early onset frontotemporal dementia and primary lateral sclerosis
-
Mackenzie IR, Feldman H. Neurofilament inclusion body disease with early onset frontotemporal dementia and primary lateral sclerosis. Clin Neuropathol 2004; 23: 183-93.
-
(2004)
Clin Neuropathol
, vol.23
, pp. 183-193
-
-
Mackenzie, I.R.1
Feldman, H.2
-
34
-
-
33749668518
-
Dementia lacking distinctive histology (DLDH) revisited
-
Mackenzie IRA, Shi J, Shaw CL, DuPlessis D, Neary D, Snowden JS, et al. Dementia lacking distinctive histology (DLDH) revisited. Acta Neuropathol 2006c; 112: 539-49.
-
(2006)
Acta Neuropathol
, vol.112
, pp. 539-549
-
-
Mackenzie, I.R.A.1
Shi, J.2
Shaw, C.L.3
DuPlessis, D.4
Neary, D.5
Snowden, J.S.6
-
35
-
-
0034764622
-
Clinical and pathological criteria for fronto-temporal dementia
-
McKhann GM, Albert MS, Grossman M, Miller B, Dickson D, Trojanowski JQ. Clinical and pathological criteria for fronto-temporal dementia. Arch Neurol 2001; 58: 1803-9.
-
(2001)
Arch Neurol
, vol.58
, pp. 1803-1809
-
-
McKhann, G.M.1
Albert, M.S.2
Grossman, M.3
Miller, B.4
Dickson, D.5
Trojanowski, J.Q.6
-
36
-
-
27744554553
-
Depletion of TDP43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene
-
Mercado PA, Ayala YM, Romano M, Buratti E, Baralle FE. Depletion of TDP43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene. Nucleic Acids Res 2005; 33: 6000-10.
-
(2005)
Nucleic Acids Res
, vol.33
, pp. 6000-6010
-
-
Mercado, P.A.1
Ayala, Y.M.2
Romano, M.3
Buratti, E.4
Baralle, F.E.5
-
37
-
-
27944473999
-
Neuronal intranuclear inclusions are ultrastructurally and immunologically distinct from cytoplasmic inclusions of neuronal intermediate filament inclusion disease
-
Mosaheb S, Thorpe JR, Hashemzadeh-Bonehi L, Bigio EH, Gearing M, Cairns NJ. Neuronal intranuclear inclusions are ultrastructurally and immunologically distinct from cytoplasmic inclusions of neuronal intermediate filament inclusion disease. Acta Neuropathol 2005; 110: 360-8.
-
(2005)
Acta Neuropathol
, vol.110
, pp. 360-368
-
-
Mosaheb, S.1
Thorpe, J.R.2
Hashemzadeh-Bonehi, L.3
Bigio, E.H.4
Gearing, M.5
Cairns, N.J.6
-
38
-
-
0021171969
-
Classic and generalized variants of Pick's disease: A clinicopathological, ultrastructural, and immunocytochemical comparative study
-
Munoz-Garcia D, Ludwin SK. Classic and generalized variants of Pick's disease: a clinicopathological, ultrastructural, and immunocytochemical comparative study. Ann Neurol 1984; 16: 467-80.
-
(1984)
Ann Neurol
, vol.16
, pp. 467-480
-
-
Munoz-Garcia, D.1
Ludwin, S.K.2
-
39
-
-
34547733547
-
Co-morbidity of TDP-43 proteinopathy in Lewy body related diseases
-
Nakashima-Yasuda H, Uryu K, Robinson J, Xie SX, Hurtig H, Duda JE, et al. Co-morbidity of TDP-43 proteinopathy in Lewy body related diseases. Acta Neuropathol 2007; 114: 221-9.
-
(2007)
Acta Neuropathol
, vol.114
, pp. 221-229
-
-
Nakashima-Yasuda, H.1
Uryu, K.2
Robinson, J.3
Xie, S.X.4
Hurtig, H.5
Duda, J.E.6
-
40
-
-
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: 1546-54.
-
(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
-
41
-
-
35348853257
-
TDP-43 proteinopathy in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Neumann M, Kwong LK, Sampathu DM, Trojanowski JQ, Lee VMY. TDP-43 proteinopathy in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Arch Neurol 2007a; 64: 1388-94.
-
(2007)
Arch Neurol
, vol.64
, pp. 1388-1394
-
-
Neumann, M.1
Kwong, L.K.2
Sampathu, D.M.3
Trojanowski, J.Q.4
Lee, V.M.Y.5
-
42
-
-
34247123666
-
TDP-43-positive white matter pathology in frontotemporal lobar degeneration with ubiquitin-positive inclusions
-
Neumann M, Kwong LK, Traux AC, Vanmassenhove B, Kretzschmar HA, Van Deerlin, et al. TDP-43-positive white matter pathology in frontotemporal lobar degeneration with ubiquitin-positive inclusions. J Neuropathol Exp Neurol 2007b; 66: 177-83.
-
(2007)
J Neuropathol Exp Neurol
, vol.66
, pp. 177-183
-
-
Neumann, M.1
Kwong, L.K.2
Traux, A.C.3
Vanmassenhove, B.4
Kretzschmar, H.A.5
Deerlin, V.6
-
43
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, Chou TT, et al. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 2006; 314: 130-3.
-
(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
-
44
-
-
0026756463
-
Ubiquitin-positive intraneuronal inclusions in the extramotor cortices of presenile dementia patients with motor neuron disease
-
Okamoto K, Murakami N, Kusaka H, Yoshida M, Hashizume Y, Nakazato Y, et al. Ubiquitin-positive intraneuronal inclusions in the extramotor cortices of presenile dementia patients with motor neuron disease. J Neurol 1992; 239: 426-30.
-
(1992)
J Neurol
, vol.239
, pp. 426-430
-
-
Okamoto, K.1
Murakami, N.2
Kusaka, H.3
Yoshida, M.4
Hashizume, Y.5
Nakazato, Y.6
-
45
-
-
33749006845
-
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)
-
Parkinson N, Ince PG, Smith MO, Highley R, Skibinski G, Anderson PM, et al. ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B). Neurology 2006; 67: 1074-7.
-
(2006)
Neurology
, vol.67
, pp. 1074-1077
-
-
Parkinson, N.1
Ince, P.G.2
Smith, M.O.3
Highley, R.4
Skibinski, G.5
Anderson, P.M.6
-
46
-
-
34848856633
-
Hippocampal sclerosis dementia: A reappraisal
-
Probst A, Taylor KI, Tolnay M. Hippocampal sclerosis dementia: a reappraisal. Acta Neuropathol 2007; 114: 335-45.
-
(2007)
Acta Neuropathol
, vol.114
, pp. 335-345
-
-
Probst, A.1
Taylor, K.I.2
Tolnay, M.3
-
47
-
-
34548737197
-
The genetics of frontotemporal lobar degeneration
-
Rademakers R, Hutton M. The genetics of frontotemporal lobar degeneration. Curr Neurol Neurosci Rep 2007; 7: 434-42.
-
(2007)
Curr Neurol Neurosci Rep
, vol.7
, pp. 434-442
-
-
Rademakers, R.1
Hutton, M.2
-
48
-
-
0041320789
-
Frontotemporal dementia in The Netherlands: Patient characteristics and prevalence estimates from a population-based study
-
Rosso SM, Donker KL, Baks T, Joosse M, de Koning I, Pijnenburg Y, et al. Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study. Brain 2003; 126: 2016-22.
-
(2003)
Brain
, vol.126
, pp. 2016-2022
-
-
Rosso, S.M.1
Donker, K.L.2
Baks, T.3
Joosse, M.4
de Koning, I.5
Pijnenburg, Y.6
-
49
-
-
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, et al. Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies. Am J Pathol 2006; 169: 1343-52.
-
(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
-
50
-
-
37349034999
-
Evidence that TDP-43 is not the major ubiquitinated target within the pathological inclusions of amyotrophic lateral sclerosis
-
Sanelli T, Xiao S, Horne P, Bilbao J, Zinman L, Robertson J. Evidence that TDP-43 is not the major ubiquitinated target within the pathological inclusions of amyotrophic lateral sclerosis. J Neuropathol Exp Neurol 2007; 66: 1147-53.
-
(2007)
J Neuropathol Exp Neurol
, vol.66
, pp. 1147-1153
-
-
Sanelli, T.1
Xiao, S.2
Horne, P.3
Bilbao, J.4
Zinman, L.5
Robertson, J.6
-
51
-
-
0031800415
-
Familial aggregation in frontotemporal dementia
-
Stevens M, van Duijn CM, Kamphorst W, de Knijff P, Heutink P, van Gool WA, et al. Familial aggregation in frontotemporal dementia. Neurology 1998; 50: 1541-5.
-
(1998)
Neurology
, vol.50
, pp. 1541-1545
-
-
Stevens, M.1
van Duijn, C.M.2
Kamphorst, W.3
de Knijff, P.4
Heutink, P.5
van Gool, W.A.6
-
52
-
-
34249751076
-
TDP-43 is a human low molecular weight neurofilament (hNFL) mRNA-binding protein
-
Strong MJ, Volkening K, Hammond R, Yang W, Strong W, Leystra-Lantz C, et al. TDP-43 is a human low molecular weight neurofilament (hNFL) mRNA-binding protein. Mol Cell Neurosci 2007; 35: 320-7.
-
(2007)
Mol Cell Neurosci
, vol.35
, pp. 320-327
-
-
Strong, M.J.1
Volkening, K.2
Hammond, R.3
Yang, W.4
Strong, W.5
Leystra-Lantz, C.6
-
53
-
-
0035209337
-
Update on the neuropathological diagnosis of frontotemporal dementia
-
Trojanowski JQ, Dickson D. Update on the neuropathological diagnosis of frontotemporal dementia. J Neuropathol Exp Neurol 2001; 60: 1123-6.
-
(2001)
J Neuropathol Exp Neurol
, vol.60
, pp. 1123-1126
-
-
Trojanowski, J.Q.1
Dickson, D.2
-
54
-
-
0035083369
-
Familial amyotrophic lateral sclerosis with posterior column degeneration and basophilic inclusion bodies: A clinical, genetic and pathological study
-
Tsuchiya K, Matsunaga T, Aoki M, Haga C, Ooe K, Abe K, et al. Familial amyotrophic lateral sclerosis with posterior column degeneration and basophilic inclusion bodies: a clinical, genetic and pathological study. Clin Neuropathol 2001; 20: 53-9.
-
(2001)
Clin Neuropathol
, vol.20
, pp. 53-59
-
-
Tsuchiya, K.1
Matsunaga, T.2
Aoki, M.3
Haga, C.4
Ooe, K.5
Abe, K.6
-
55
-
-
0026691337
-
Hippocampal and neocortical ubiquitin-immunoreactive inclusions in amyotrophic lateral sclerosis with dementia
-
Wightman G, Anderson VER, Martin J, Swash M, Anderton BH, Neary D, et al. Hippocampal and neocortical ubiquitin-immunoreactive inclusions in amyotrophic lateral sclerosis with dementia. Neurosci Lett 1992; 139: 269-74.
-
(1992)
Neurosci Lett
, vol.139
, pp. 269-274
-
-
Wightman, G.1
Anderson, V.E.R.2
Martin, J.3
Swash, M.4
Anderton, B.H.5
Neary, D.6
-
56
-
-
33846262456
-
Abnormalities of the nucleus and nuclear inclusions in neurodegenerative disease: A work in progress
-
Woulfe JM. Abnormalities of the nucleus and nuclear inclusions in neurodegenerative disease: a work in progress. Neuopathol Appl Neurobiol 2007; 33: 2-42.
-
(2007)
Neuopathol Appl Neurobiol
, vol.33
, pp. 2-42
-
-
Woulfe, J.M.1
-
57
-
-
85039774539
-
Basophilic inclusion body disease and neuronal intermediate filament inclusion disease: A comparative clinicopathological study
-
in press
-
Yokota O, Tsuchiya K, Terada S, Ishizu H, Uchikado H, Ikeda M, et al. Basophilic inclusion body disease and neuronal intermediate filament inclusion disease: a comparative clinicopathological study. Acta Neuropathol (in press).
-
Acta Neuropathol
-
-
Yokota, O.1
Tsuchiya, K.2
Terada, S.3
Ishizu, H.4
Uchikado, H.5
Ikeda, M.6
|