-
1
-
-
33750716074
-
TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
DOI 10.1016/j.bbrc.2006.10.093, PII S0006291X06023187
-
Arai T, Hasegawa M, Akiyama H 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 (Pubitemid 44708852)
-
(2006)
Biochemical and Biophysical Research Communications
, vol.351
, Issue.3
, 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
Oda, T.11
-
2
-
-
65649112431
-
TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration
-
Benajiba L, Le Ber I, Camuzat A et al (2009) TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration. Ann Neurol 65:470-473
-
(2009)
Ann. Neurol.
, vol.65
, pp. 470-473
-
-
Benajiba, L.1
Le Ber, I.2
Camuzat, A.3
-
3
-
-
0029013727
-
Staging of Alzheimer's disease-related neurofibrillary changes
-
discussion 278-284
-
Braak H, Braak E (1995) Staging of Alzheimer's disease-related neurofibrillary changes. Neurobiol Aging 16:271-278 discussion 278-284
-
(1995)
Neurobiol. Aging
, vol.16
, pp. 271-278
-
-
Braak, H.1
Braak, E.2
-
4
-
-
36949024480
-
Severe subcortical TDP-43 pathology in sporadic frontotemporal lobar degeneration with motor neuron disease
-
DOI 10.1007/s00401-007-0315-5
-
Brandmeir NJ, Geser F, Kwong LK et al (2008) Severe subcortical TDP-43 pathology in sporadic frontotemporal lobar degeneration with motor neuron disease. Acta Neuropathol 115:123-131 (Pubitemid 50003187)
-
(2008)
Acta Neuropathologica
, vol.115
, Issue.1
, pp. 123-131
-
-
Brandmeir, N.J.1
Geser, F.2
Kwong, L.K.3
Zimmerman, E.4
Qian, J.5
Lee, V.M.-Y.6
Trojanowski, J.Q.7
-
6
-
-
0032692481
-
The ALSFRS-R: A revised ALS functional rating scale that incorporates assessments of respiratory function
-
DOI 10.1016/S0022-510X(99)00210-5, PII S0022510X99002105
-
Cedarbaum JM, Stambler N, Malta E et al (1999) The ALSFRSR: a revised ALS functional rating scale that incorporates assessments of respiratory function. BDNF ALS Study Group (Phase III). J Neurol Sci 169:13-21 (Pubitemid 29502501)
-
(1999)
Journal of the Neurological Sciences
, vol.169
, Issue.1-2
, pp. 13-21
-
-
Cedarbaum, J.M.1
Stambler, N.2
Malta, E.3
Fuller, C.4
Hilt, D.5
Thurmond, B.6
Nakanishi, A.7
-
8
-
-
64549117768
-
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis
-
Chio A, Schymick JC, Restagno G et al (2009) A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. Hum Mol Genet 18:1524-1532
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 1524-1532
-
-
Chio, A.1
Schymick, J.C.2
Restagno, G.3
-
9
-
-
41249089087
-
Loss of progranulin function in frontotemporal lobar degeneration
-
Cruts M, Van Broeckhoven C (2008) Loss of progranulin function in frontotemporal lobar degeneration. Trends Genet 24:186-194
-
(2008)
Trends Genet.
, vol.24
, pp. 186-194
-
-
Cruts, M.1
Van Broeckhoven, C.2
-
10
-
-
34548083742
-
Whole-genome analysis of sporadic amyotrophic lateral sclerosis
-
Dunckley T, Huentelman MJ, Craig DW et al (2007) Wholegenome analysis of sporadic amyotrophic lateral sclerosis. N Engl J Med 357:775-788 (Pubitemid 47295644)
-
(2007)
New England Journal of Medicine
, vol.357
, Issue.8
, pp. 775-788
-
-
Dunckley, T.1
Huentelman, M.J.2
Craig, D.W.3
Pearson, J.V.4
Szelinger, S.5
Joshipura, K.6
Halperin, R.F.7
Stamper, C.8
Jensen, K.R.9
Letizia, D.10
Hesterlee, S.E.11
Pestronk, A.12
Levine, T.13
Bertorini, T.14
Graves, M.C.15
Mozaffar, T.16
Jackson, C.E.17
Bosch, P.18
McVey, A.19
Dick, A.20
Barohn, R.21
Lomen-Hoerth, C.22
Rosenfeld, J.23
O'Connor, D.T.24
Zhang, K.25
Crook, R.26
Ryberg, H.27
Hutton, M.28
Katz, J.29
Simpson, E.P.30
Mitsumoto, H.31
Bowser, R.32
Miller, R.G.33
Appel, S.H.34
Stephan, D.A.35
more..
-
11
-
-
43549091368
-
Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis
-
DOI 10.1001/archneur.65.5.636
-
Geser F, Brandmeir NJ, Kwong LK et al (2008) Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis. Arch Neurol 65:636-641 (Pubitemid 351679659)
-
(2008)
Archives of Neurology
, vol.65
, Issue.5
, pp. 636-641
-
-
Geser, F.1
Brandmeir, N.J.2
Kwong, L.K.3
Martinez-Lage, M.4
Elman, L.5
McCluskey, L.6
Xie, S.X.7
Lee, V.M.-Y.8
Trojanowski, J.Q.9
-
12
-
-
60549117972
-
Clinical and pathological continuum of multisystem TDP-43 proteinopathies
-
Geser F, Martinez-Lage M, Robinson J et al (2009) Clinical and pathological continuum of multisystem TDP-43 proteinopathies. Arch Neurol 66:180-189
-
(2009)
Arch. Neurol.
, vol.66
, pp. 180-189
-
-
Geser, F.1
Martinez-Lage, M.2
Robinson, J.3
-
13
-
-
41949119043
-
TDP-43 A315T mutation in familial motor neuron disease
-
DOI 10.1002/ana.21344
-
Gitcho MA, Baloh RH, Chakraverty S et al (2008) TDP-43 A315T mutation in familial motor neuron disease. Ann Neurol 63:535-538 (Pubitemid 351614720)
-
(2008)
Annals of Neurology
, vol.63
, Issue.4
, 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 III, C.L.8
Bigio, E.H.9
Caselli, R.10
Baker, M.11
Al-Lozi, M.T.12
Morris, J.C.13
Pestronk, A.14
Rademakers, R.15
Goate, A.M.16
Cairns, N.J.17
-
14
-
-
4444248435
-
Clinicopathological correlates in frontotemporal dementia
-
DOI 10.1002/ana.20203
-
Hodges JR, Davies RR, Xuereb JH et al (2004) Clinicopathological correlates in frontotemporal dementia. Ann Neurol 56:399-406 (Pubitemid 39166559)
-
(2004)
Annals of Neurology
, vol.56
, Issue.3
, pp. 399-406
-
-
Hodges, J.R.1
Davies, R.R.2
Xuereb, J.H.3
Casey, B.4
Broe, M.5
Bak, T.H.6
Kril, J.J.7
Halliday, G.M.8
-
15
-
-
42649120983
-
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
-
DOI 10.1038/ng.132, PII NG132
-
Kabashi E, Valdmanis PN, Dion P et al (2008) TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nat Genet 40:572-574 (Pubitemid 351601218)
-
(2008)
Nature Genetics
, vol.40
, Issue.5
, pp. 572-574
-
-
Kabashi, E.1
Valdmanis, P.N.2
Dion, P.3
Spiegelman, D.4
McConkey, B.J.5
Velde, C.V.6
Bouchard, J.-P.7
Lacomblez, L.8
Pochigaeva, K.9
Salachas, F.10
Pradat, P.-F.11
Camu, W.12
Meininger, V.13
Dupre, N.14
Rouleau, G.A.15
-
17
-
-
36448996185
-
Screening for frontotemporal dementias and Alzheimer's disease with the Philadelphia brief assessment of cognition: A preliminary analysis
-
DOI 10.1159/000110577
-
Libon DJ, Massimo L, Moore P et al (2007) Screening for frontotemporal dementias and Alzheimer's disease with the Philadelphia Brief Assessment of Cognition: a preliminary analysis. Dement Geriatr Cogn Disord 24:441-447 (Pubitemid 350175904)
-
(2007)
Dementia and Geriatric Cognitive Disorders
, vol.24
, Issue.6
, pp. 441-447
-
-
Libon, D.J.1
Massimo, L.2
Moore, P.3
Coslett, H.B.4
Chatterjee, A.5
Aguirre, G.K.6
Rice, A.7
Vesely, L.8
Grossman, M.9
-
18
-
-
0037426388
-
Are amyotrophic lateral sclerosis patients cognitively normal?
-
Lomen-Hoerth C, Murphy J, Langmore S et al (2003) Are amyotrophic lateral sclerosis patients cognitively normal? Neurology 60:1094-1097 (Pubitemid 36418766)
-
(2003)
Neurology
, vol.60
, Issue.7
, pp. 1094-1097
-
-
Lomen-Hoerth, C.1
Murphy, J.2
Langmore, S.3
Kramer, J.H.4
Olney, R.K.5
Miller, B.6
-
19
-
-
57049105123
-
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: Consensus recommendations
-
Mackenzie IR, Neumann M, Bigio EH et al (2009) Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations. Acta Neuropathol 117:15-18
-
(2009)
Acta Neuropathol.
, vol.117
, pp. 15-18
-
-
Mackenzie, I.R.1
Neumann, M.2
Bigio, E.H.3
-
20
-
-
34247147601
-
Continuum of frontal lobe impairment in amyotrophic lateral sclerosis
-
Murphy JM, Henry RG, Langmore S et al (2007) Continuum of frontal lobe impairment in amyotrophic lateral sclerosis. Arch Neurol 64:530-534 (Pubitemid 46588341)
-
(2007)
Archives of Neurology
, vol.64
, Issue.4
, pp. 530-534
-
-
Murphy, J.M.1
Henry, R.G.2
Langmore, S.3
Kramer, J.H.4
Miller, B.L.5
Lomen-Hoerth, C.6
-
21
-
-
0031672540
-
Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria
-
Neary D, Snowden JS, Gustafson L et al (1998) Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology 51:1546-1554
-
(1998)
Neurology
, vol.51
, pp. 1546-1554
-
-
Neary, D.1
Snowden, J.S.2
Gustafson, L.3
-
22
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
DOI 10.1126/science.1134108
-
Neumann M, Sampathu DM, Kwong LK et al (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314:130-133 (Pubitemid 44547757)
-
(2006)
Science
, vol.314
, Issue.5796
, 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
McCluskey, L.F.11
Miller, B.L.12
Masliah, E.13
Mackenzie, I.R.14
Feldman, H.15
Feiden, W.16
Kretzschmar, H.A.17
Trojanowski, J.Q.18
Lee, V.M.-Y.19
-
23
-
-
77649252528
-
Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis
-
Pesiridis GS, Lee VM-Y, Trojanowski JQ (2009) Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis. Hum Mol Genet 18 (R2): R156-R162
-
(2009)
Hum. Mol. Genet.
, vol.18
, Issue.R2
-
-
Pesiridis, G.S.1
Lee, V.M.-Y.2
Trojanowski, J.Q.3
-
24
-
-
35248823549
-
Cognitive impairment in amyotrophic lateral sclerosis
-
DOI 10.1016/S1474-4422(07)70265-X, PII S147444220770265X
-
Phukan J, Pender NP, Hardiman O (2007) Cognitive impairment in amyotrophic lateral sclerosis. Lancet Neurol 6:994-1003 (Pubitemid 47562321)
-
(2007)
Lancet Neurology
, vol.6
, Issue.11
, pp. 994-1003
-
-
Phukan, J.1
Pender, N.P.2
Hardiman, O.3
-
25
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
DOI 10.1126/science.1154584
-
Sreedharan J, Blair IP, Tripathi VB et al (2008) TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 319:1668-1672 (Pubitemid 351432505)
-
(2008)
Science
, vol.319
, Issue.5870
, 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
Baralle, F.11
De Belleroche, J.12
Mitchell, J.D.13
Leigh, P.N.14
Al-Chalabi, A.15
Miller, C.C.16
Nicholson, G.17
Shaw, C.E.18
-
26
-
-
67651160559
-
Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis
-
Strong MJ, Grace GM, Freedman M et al (2009) Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis. Amyotroph Lateral Scler 10:131-146
-
(2009)
Amyotroph Lateral Scler
, vol.10
, pp. 131-146
-
-
Strong, M.J.1
Grace, G.M.2
Freedman, M.3
-
27
-
-
57049182428
-
Progression of hippocampal degeneration in amyotrophic lateral sclerosis with or without memory impairment: Distinction from Alzheimer disease
-
Takeda T, Uchihara T, Arai N, Mizutani T, Iwata M (2009) Progression of hippocampal degeneration in amyotrophic lateral sclerosis with or without memory impairment: distinction from Alzheimer disease. Acta Neuropathol 117:35-44
-
(2009)
Acta Neuropathol.
, vol.117
, pp. 35-44
-
-
Takeda, T.1
Uchihara, T.2
Arai, N.3
Mizutani, T.4
Iwata, M.5
-
28
-
-
12344293448
-
Survival of 793 patients with amyotrophic lateral sclerosis diagnosed over a 28-year period
-
DOI 10.1080/14660820410021311
-
Testa D, Lovati R, Ferrarini M, Salmoiraghi F, Filippini G (2004) Survival of 793 patients with amyotrophic lateral sclerosis diagnosed over a 28-year period. Amyotroph Lateral Scler Other Motor Neuron Disord 5:208-212 (Pubitemid 40125186)
-
(2004)
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders
, vol.5
, Issue.4
, pp. 208-212
-
-
Testa, D.1
Lovati, R.2
Ferrarini, M.3
Salmoiraghi, F.4
Filippini, G.5
-
29
-
-
77649136250
-
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
-
Van Deerlin VM, Sleiman PM, Martinez-Lage 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.2
Martinez-Lage, M.3
-
30
-
-
41949100148
-
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: A genetic and histopathological analysis
-
Van Deerlin VM, Leverenz JB, Bekris LM et al (2008) TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis. Lancet Neurol 7:409-416
-
(2008)
Lancet Neurol.
, vol.7
, pp. 409-416
-
-
Van Deerlin, V.M.1
Leverenz, J.B.2
Bekris, L.M.3
-
31
-
-
79954440990
-
Building an integrated neurodegenerative disease database at an academic health center
-
Xie SX, Baek Y, Grossman M et al (2010) Building an integrated neurodegenerative disease database at an academic health center. Alzheimers Dement (in press)
-
(2010)
Alzheimers Dement (in press)
-
-
Xie, S.X.1
Baek, Y.2
Grossman, M.3
|