-
1
-
-
84865843186
-
The genetics and neuropathology of amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BC38Xht1egt7vF, PID: 22903397
-
Al-Chalabi A, Jones A, Troakes C, King A, Al-Sarraj S, van den Berg LH (2012) The genetics and neuropathology of amyotrophic lateral sclerosis. Acta Neuropathol 124:339–352
-
(2012)
Acta Neuropathol
, vol.124
, pp. 339-352
-
-
Al-Chalabi, A.1
Jones, A.2
Troakes, C.3
King, A.4
Al-Sarraj, S.5
van den Berg, L.H.6
-
2
-
-
0019781601
-
Unifying hypothesis for the cause of amyotrophic lateral sclerosis, Parkinsonism and Alzheimer disease
-
COI: 1:STN:280:DyaL387ht1Sgug%3D%3D, PID: 6173010
-
Appel SH (1981) Unifying hypothesis for the cause of amyotrophic lateral sclerosis, Parkinsonism and Alzheimer disease. Ann Neurol 10:499–505
-
(1981)
Ann Neurol
, vol.10
, pp. 499-505
-
-
Appel, S.H.1
-
3
-
-
33750716074
-
TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BD28Xht1SmsbbJ, PID: 17084815
-
Arai T, Hasegawa M, Akiyama H, Ikeda K, Nonaka T, Mori 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
-
(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
-
4
-
-
59549094064
-
Structural determinants of the cellular localization and shuttling of TDP-43
-
COI: 1:CAS:528:DC%2BD1cXhsFaktLjM, PID: 18957508
-
Ayala YM, Zago P, D’Ambrogio D, Xu YF, Buratti E et al (2008) Structural determinants of the cellular localization and shuttling of TDP-43. J Cell Sci 121:3778–3785
-
(2008)
J Cell Sci
, vol.121
, pp. 3778-3785
-
-
Ayala, Y.M.1
Zago, P.2
D’Ambrogio, D.3
Xu, Y.F.4
Buratti, E.5
-
7
-
-
0001785453
-
Architectonics as seen by lipofuscin stains
-
Jones EG, Peters A, (eds), Plenum Press, New York
-
Braak H (1984) Architectonics as seen by lipofuscin stains. In: Jones EG, Peters A (eds) Cerebral cortex. Cellular components of the cerebral cortex, Vol I. Plenum Press, New York, pp 59–104
-
(1984)
Cerebral cortex. Cellular components of the cerebral cortex, Vol I
, pp. 59-104
-
-
Braak, H.1
-
8
-
-
0026134421
-
Demonstration of amyloid deposits and neurofibrillary changes in whole brain sections
-
COI: 1:STN:280:DyaK2c7it12msQ%3D%3D, PID: 1669710
-
Braak H, Braak E (1991) Demonstration of amyloid deposits and neurofibrillary changes in whole brain sections. Brain Pathol 1:213–216
-
(1991)
Brain Pathol
, vol.1
, pp. 213-216
-
-
Braak, H.1
Braak, E.2
-
9
-
-
0037333666
-
Staging of brain pathology related to sporadic Parkinson’s disease
-
PID: 12498954
-
Braak H, Del Tredici K, Rüb U, de Vos RA, Jansen Steur EN, Braak E (2003) Staging of brain pathology related to sporadic Parkinson’s disease. Neurobiol Aging 24:197–211
-
(2003)
Neurobiol Aging
, vol.24
, pp. 197-211
-
-
Braak, H.1
Del Tredici, K.2
Rüb, U.3
de Vos, R.A.4
Jansen Steur, E.N.5
Braak, E.6
-
10
-
-
77953870938
-
Amyotrophic lateral sclerosis: dash-like inclusions of phosphorylated TDP-43 in somatodendritic and axonal compartments of somatomotor neurons of the lower brainstem and spinal cord
-
COI: 1:CAS:528:DC%2BC3cXns1ymurY%3D, PID: 20379728
-
Braak H, Ludolph AC, Thal DR, Del Tredici K (2010) Amyotrophic lateral sclerosis: dash-like inclusions of phosphorylated TDP-43 in somatodendritic and axonal compartments of somatomotor neurons of the lower brainstem and spinal cord. Acta Neuropathol 120:67–74
-
(2010)
Acta Neuropathol
, vol.120
, pp. 67-74
-
-
Braak, H.1
Ludolph, A.C.2
Thal, D.R.3
Del Tredici, K.4
-
11
-
-
80054904670
-
Stages of the pathologic process in Alzheimer disease: age categories from 1 to 100 years
-
COI: 1:CAS:528:DC%2BC3MXhtlChs7bJ, PID: 22002422
-
Braak H, Thal DR, Ghebremedhin E, Del Tredici K (2011) Stages of the pathologic process in Alzheimer disease: age categories from 1 to 100 years. J Neuropathol Exp Neurol 70:960–969
-
(2011)
J Neuropathol Exp Neurol
, vol.70
, pp. 960-969
-
-
Braak, H.1
Thal, D.R.2
Ghebremedhin, E.3
Del Tredici, K.4
-
12
-
-
84890121734
-
Amyotrophic lateral sclerosis––a model of corticofugal axonal spread
-
COI: 1:CAS:528:DC%2BC3sXhslygurrK, PID: 24217521
-
Braak H, Brettschneider J, Ludolph AC, Lee VM, Trojanowski JQ, Del Tredici K (2013) Amyotrophic lateral sclerosis––a model of corticofugal axonal spread. Nat Rev Neurol 9:708–714
-
(2013)
Nat Rev Neurol
, vol.9
, pp. 708-714
-
-
Braak, H.1
Brettschneider, J.2
Ludolph, A.C.3
Lee, V.M.4
Trojanowski, J.Q.5
Del Tredici, K.6
-
13
-
-
84883292041
-
Stages of pTDP-43 pathology in amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BC3sXhtlKku7jE, PID: 23686809
-
Brettschneider J, Del Tredici K, Toledo JB, Robinson JL, Irwin DJ, Grossman M et al (2013) Stages of pTDP-43 pathology in amyotrophic lateral sclerosis. Ann Neurol 74:20–38
-
(2013)
Ann Neurol
, vol.74
, pp. 20-38
-
-
Brettschneider, J.1
Del Tredici, K.2
Toledo, J.B.3
Robinson, J.L.4
Irwin, D.J.5
Grossman, M.6
-
15
-
-
0025945768
-
The role of axonal transport in neurodegenerative disease spread: a meta-analysis of experimental and clinical poliomyelitis compares with amyotrophic lateral sclerosis
-
COI: 1:STN:280:DyaK38%2FjsVCrsg%3D%3D, PID: 1718581
-
Brooks BR (1991) The role of axonal transport in neurodegenerative disease spread: a meta-analysis of experimental and clinical poliomyelitis compares with amyotrophic lateral sclerosis. Can J Neurol Sci 18(Suppl 3):435–438
-
(1991)
Can J Neurol Sci
, vol.18
, pp. 435-438
-
-
Brooks, B.R.1
-
16
-
-
0034574407
-
El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis
-
COI: 1:STN:280:DC%2BD3Mvhs1Ghsg%3D%3D, PID: 11464847
-
Brooks BR, Miller RG, Swash M, Munsat TL, World Federation of Neurology Research Group on Motor Neuron Diseases (2000) El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord 1:293–299
-
(2000)
Amyotroph Lateral Scler Other Motor Neuron Disord
, vol.1
, pp. 293-299
-
-
Brooks, B.R.1
Miller, R.G.2
Swash, M.3
Munsat, T.L.4
-
17
-
-
26444570938
-
The extraocular motor nuclei: organization and functional neuroanatomy
-
PID: 16221587
-
Büttner-Ennever JA (2006) The extraocular motor nuclei: organization and functional neuroanatomy. Prog Brain Res 151:95–125
-
(2006)
Prog Brain Res
, vol.151
, pp. 95-125
-
-
Büttner-Ennever, J.A.1
-
18
-
-
0027296350
-
Aymotrophic lateral sclerosis: lower motor neuron disease spreading to upper motor neurons
-
COI: 1:STN:280:DyaK3szitl2isQ%3D%3D, PID: 8332139
-
Chou SM, Norris FH (1993) Aymotrophic lateral sclerosis: lower motor neuron disease spreading to upper motor neurons. Muscle Nerve 16:864–869
-
(1993)
Muscle Nerve
, vol.16
, pp. 864-869
-
-
Chou, S.M.1
Norris, F.H.2
-
19
-
-
58249089343
-
Age-dependent deterioration of nuclear pore complexes causes a loss of nuclear integrity in postmitotic cells
-
PID: 19167330
-
D’Angelo MA, Raices M, Panowski SH, Hetzer MW (2009) Age-dependent deterioration of nuclear pore complexes causes a loss of nuclear integrity in postmitotic cells. Cell 136:284–295
-
(2009)
Cell
, vol.136
, pp. 284-295
-
-
D’Angelo, M.A.1
Raices, M.2
Panowski, S.H.3
Hetzer, M.W.4
-
20
-
-
0035079788
-
The motor cortex and amyotrophic lateral sclerosis
-
COI: 1:STN:280:DC%2BD3M7ntVSqsw%3D%3D, PID: 11268031
-
Eisen A, Weber M (2001) The motor cortex and amyotrophic lateral sclerosis. Muscle Nerve 24:564–579
-
(2001)
Muscle Nerve
, vol.24
, pp. 564-579
-
-
Eisen, A.1
Weber, M.2
-
21
-
-
84920901644
-
Conformation determines the seeding potencies of native and recombinant tau aggregates
-
COI: 1:CAS:528:DC%2BC2MXpvFanuw%3D%3D, PID: 25406315
-
Falcon B, Cavallini A, Angers R, Glover S, Murray TK, Barnham L et al (2015) Conformation determines the seeding potencies of native and recombinant tau aggregates. J Biol Chem 290:1049–1065
-
(2015)
J Biol Chem
, vol.290
, pp. 1049-1065
-
-
Falcon, B.1
Cavallini, A.2
Angers, R.3
Glover, S.4
Murray, T.K.5
Barnham, L.6
-
22
-
-
84865063851
-
The ALS disease protein TDP-43 is actively transported in motor neuron axons and regulates axon outgrowth
-
Fallini C, Bassell G, Rossoll W (2012) The ALS disease protein TDP-43 is actively transported in motor neuron axons and regulates axon outgrowth. Hum Mol Genet 21:3708–3718
-
(2012)
Hum Mol Genet
, vol.21
, pp. 3708-3718
-
-
Fallini, C.1
Bassell, G.2
Rossoll, W.3
-
23
-
-
85018209399
-
Spread of pathology in amyotrophic lateral sclerosis: assessment of phosphorylated TDP-43 along axonal pathways
-
PID: 26216351
-
Fatima M, Tan R, Halliday GM, Kril JJ (2015) Spread of pathology in amyotrophic lateral sclerosis: assessment of phosphorylated TDP-43 along axonal pathways. Acta Neuropathol Commun 3:47
-
(2015)
Acta Neuropathol Commun
, vol.3
, pp. 47
-
-
Fatima, M.1
Tan, R.2
Halliday, G.M.3
Kril, J.J.4
-
24
-
-
84970952328
-
TDP-43 is intercellularly transmitted across axon terminals
-
COI: 1:CAS:528:DC%2BC28XpsV2ltrg%3D, PID: 26598621
-
Feiler MS, Strobel B, Freischmidt A, Helferich AM, Kappel J, Brewer BM et al (2015) TDP-43 is intercellularly transmitted across axon terminals. J Cell Biol 211:897–911
-
(2015)
J Cell Biol
, vol.211
, pp. 897-911
-
-
Feiler, M.S.1
Strobel, B.2
Freischmidt, A.3
Helferich, A.M.4
Kappel, J.5
Brewer, B.M.6
-
25
-
-
0345742771
-
Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man
-
PID: 14736504
-
Fischer LR, Culver DG, Tennant P, Davis AA, Wang M, Castellano-Sanchez A et al (2004) Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man. Exp Neurol 185:232–240
-
(2004)
Exp Neurol
, vol.185
, pp. 232-240
-
-
Fischer, L.R.1
Culver, D.G.2
Tennant, P.3
Davis, A.A.4
Wang, M.5
Castellano-Sanchez, A.6
-
26
-
-
84866322476
-
Extrasynaptic neurotransmission in the modulation of brain function. Focus on the striatal neuronal-glial networks
-
COI: 1:CAS:528:DC%2BC38XptV2itrc%3D, PID: 22675301
-
Fuxe K, Borroto-Escuela DO, Romero-Fernandez W, Diaz-Cabiale Z, Rivera A, Ferraro L et al (2012) Extrasynaptic neurotransmission in the modulation of brain function. Focus on the striatal neuronal-glial networks. Front Physiol 3:136
-
(2012)
Front Physiol
, vol.3
, pp. 136
-
-
Fuxe, K.1
Borroto-Escuela, D.O.2
Romero-Fernandez, W.3
Diaz-Cabiale, Z.4
Rivera, A.5
Ferraro, L.6
-
27
-
-
43549091368
-
Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis
-
PID: 18474740
-
Geser F, Brandmeir NJ, Kwong LK, Martinez-Lage M, McCluskey L, Xie SX et al (2008) Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis. Arch Neurol 65:636–641
-
(2008)
Arch Neurol
, vol.65
, pp. 636-641
-
-
Geser, F.1
Brandmeir, N.J.2
Kwong, L.K.3
Martinez-Lage, M.4
McCluskey, L.5
Xie, S.X.6
-
28
-
-
75949105684
-
TDP-43 redistribution is an early event in sporadic amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BC3cXjs1Ggtro%3D, PID: 19338576
-
Giordana MT, Piccinini M, Grifoni S, De Marco G, Verecellino M, Magistrello M et al (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
Verecellino, M.5
Magistrello, M.6
-
29
-
-
84930452093
-
From molecule to molecule and cell to cell: prion-like mechanisms in amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BC2MXjtFegsbY%3D, PID: 25701498
-
Grad LI, Fernando SM, Cashman NR (2015) From molecule to molecule and cell to cell: prion-like mechanisms in amyotrophic lateral sclerosis. Neurobiol Dis 77:257–265
-
(2015)
Neurobiol Dis
, vol.77
, pp. 257-265
-
-
Grad, L.I.1
Fernando, S.M.2
Cashman, N.R.3
-
30
-
-
0036240957
-
Possible pathogenic role of muscle cell dysfunction in motor neuron death in spinal muscular atrophy
-
PID: 11994964
-
Guettier-Sigrist S, Hugel B, Coupin G, Freyssiner JM, Poindron P, Warter JM (2002) Possible pathogenic role of muscle cell dysfunction in motor neuron death in spinal muscular atrophy. Muscle Nerve 25:700–708
-
(2002)
Muscle Nerve
, vol.25
, pp. 700-708
-
-
Guettier-Sigrist, S.1
Hugel, B.2
Coupin, G.3
Freyssiner, J.M.4
Poindron, P.5
Warter, J.M.6
-
31
-
-
84908378481
-
Motor neuron disease and frontotemporal dementia: sometimes related, sometimes not
-
COI: 1:CAS:528:DC%2BC3sXitVWnsbjF, PID: 24246281
-
Hardy J, Rogaeva E (2014) Motor neuron disease and frontotemporal dementia: sometimes related, sometimes not. Exp Neurol 262(Pt B):75–83
-
(2014)
Exp Neurol
, vol.262
, pp. 75-83
-
-
Hardy, J.1
Rogaeva, E.2
-
32
-
-
47949086625
-
Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BD1cXhtVKnsrnM, PID: 18546284
-
Hasegawa M, Arai T, Nonaka T, Kametani F, Yoshida M, Hashizume Y 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
-
33
-
-
84960910769
-
Emergence of an imaging biomarker for amyotrophic lateral sclerosis: is the end point near?
-
PID: 26929028
-
Hornberger M, Kiernan MC (2016) Emergence of an imaging biomarker for amyotrophic lateral sclerosis: is the end point near? J Neurol Neurosurg Psychiatry 87:569
-
(2016)
J Neurol Neurosurg Psychiatry
, vol.87
, pp. 569
-
-
Hornberger, M.1
Kiernan, M.C.2
-
34
-
-
84961771361
-
Mass spectrometric analysis of accumulated TDP-43 in amyotrophic lateral sclerosis brains
-
COI: 1:CAS:528:DC%2BC28XktlKjurg%3D, PID: 26980269
-
Kametani F, Obi T, Shishido T, Akatsu H, Muryama S et al (2016) Mass spectrometric analysis of accumulated TDP-43 in amyotrophic lateral sclerosis brains. Sci Rep 6:23281
-
(2016)
Sci Rep
, vol.6
, pp. 23281
-
-
Kametani, F.1
Obi, T.2
Shishido, T.3
Akatsu, H.4
Muryama, S.5
-
35
-
-
84861841901
-
Can regional spreading of amyotrophic lateral sclerosis motor symptoms be explained by prion-like propagation?
-
PID: 22544947
-
Kanouchi T, Ohkubo T, Yokota T (2012) Can regional spreading of amyotrophic lateral sclerosis motor symptoms be explained by prion-like propagation? J Neurol Neurosurg Psychiatry 83:739–745
-
(2012)
J Neurol Neurosurg Psychiatry
, vol.83
, pp. 739-745
-
-
Kanouchi, T.1
Ohkubo, T.2
Yokota, T.3
-
36
-
-
84901475346
-
Diffusion tensor imaging analysis of sequential spreading of disease in amyotrophic lateral sclerosis confirms patterns ofTDP-43 pathology
-
PID: 24736303
-
Kassubek J, Müller HP, Del Tredici K, Brettschneider J, Pinkhardt EH, Lulé D et al (2014) Diffusion tensor imaging analysis of sequential spreading of disease in amyotrophic lateral sclerosis confirms patterns ofTDP-43 pathology. Brain 137:1733–1740
-
(2014)
Brain
, vol.137
, pp. 1733-1740
-
-
Kassubek, J.1
Müller, H.P.2
Del Tredici, K.3
Brettschneider, J.4
Pinkhardt, E.H.5
Lulé, D.6
-
37
-
-
79952486262
-
Amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BC3MXjtFWgsL8%3D, PID: 21296405
-
Kiernan MC, Vucic S, Cheah BC, Turner MR, Eisen A, Hardiman O et al (2011) Amyotrophic lateral sclerosis. Lancet 377:942–955
-
(2011)
Lancet
, vol.377
, pp. 942-955
-
-
Kiernan, M.C.1
Vucic, S.2
Cheah, B.C.3
Turner, M.R.4
Eisen, A.5
Hardiman, O.6
-
38
-
-
84856741242
-
The discovery of the pyramidal neurons: Vladimir Betz and a new era of neuroscience
-
PID: 22075067
-
Kushchayev SV, Moskalenko VF, Wiener PC, Tsymbaliuk VI, Cherkasov VG, Dzyavulska IV et al (2012) The discovery of the pyramidal neurons: Vladimir Betz and a new era of neuroscience. Brain 135:285–300
-
(2012)
Brain
, vol.135
, pp. 285-300
-
-
Kushchayev, S.V.1
Moskalenko, V.F.2
Wiener, P.C.3
Tsymbaliuk, V.I.4
Cherkasov, V.G.5
Dzyavulska, I.V.6
-
39
-
-
0000163237
-
Anatomy of the descending pathways
-
Brookhart JM, Mountcastle VB, (eds), 2, American Physiological Society, Bethesda
-
Kuypers HGJM (1981) Anatomy of the descending pathways. In: Brookhart JM, Mountcastle VB (eds) Handbook of Physiology, Neurophysiology, vol 2. American Physiological Society, Bethesda, pp 597–666
-
(1981)
Handbook of Physiology, Neurophysiology
, pp. 597-666
-
-
Kuypers, H.G.J.M.1
-
40
-
-
84956969211
-
Stabilization of & α-synuclein fibril clusters prevents fragmentation and reduces seeding activity and toxicity
-
COI: 1:CAS:528:DC%2BC28XksFSktA%3D%3D, PID: 26799377
-
Lam HT, Graber MC, Gentry KA, Bieschke J (2016) Stabilization of & α-synuclein fibril clusters prevents fragmentation and reduces seeding activity and toxicity. Biochemistry 55:675–685
-
(2016)
Biochemistry
, vol.55
, pp. 675-685
-
-
Lam, H.T.1
Graber, M.C.2
Gentry, K.A.3
Bieschke, J.4
-
41
-
-
84155167265
-
Gains or losses: molecular mechanisms of TDP43-mediated neurodegeneration
-
COI: 1:CAS:528:DC%2BC3MXhsFeqt7fP
-
Lee EB, Lee VM, Trojanowski JQ (2012) Gains or losses: molecular mechanisms of TDP43-mediated neurodegeneration. Nat Rev Neurosci 13:38–50
-
(2012)
Nat Rev Neurosci
, vol.13
, pp. 38-50
-
-
Lee, E.B.1
Lee, V.M.2
Trojanowski, J.Q.3
-
42
-
-
84941785675
-
Prion-like mechanism in amyotrophic lateral sclerosis: are protein aggregates the key?
-
PID: 25792864
-
Lee S, Kim HJ (2015) Prion-like mechanism in amyotrophic lateral sclerosis: are protein aggregates the key? Exp Neurobiol 24:1–7
-
(2015)
Exp Neurobiol
, vol.24
, pp. 1-7
-
-
Lee, S.1
Kim, H.J.2
-
43
-
-
78649907008
-
Cell-to-cell transmission of non-prion protein aggregates
-
PID: 21045796
-
Lee SJ, Desplats P, Sigurdson C, Tsigelny I, Masliah E (2010) Cell-to-cell transmission of non-prion protein aggregates. Nat Rev Neurol 6:702–706
-
(2010)
Nat Rev Neurol
, vol.6
, pp. 702-706
-
-
Lee, S.J.1
Desplats, P.2
Sigurdson, C.3
Tsigelny, I.4
Masliah, E.5
-
44
-
-
46149116992
-
Descending pathways in motor control
-
COI: 1:CAS:528:DC%2BD1cXpt12nsrg%3D, PID: 18558853
-
Lemon RN (2008) Descending pathways in motor control. Ann Rev Neurosci 31:195–218
-
(2008)
Ann Rev Neurosci
, vol.31
, pp. 195-218
-
-
Lemon, R.N.1
-
45
-
-
77955081819
-
What drives corticospinal output?
-
Lemon RN (2010) What drives corticospinal output? Biol Rep 2:51
-
(2010)
Biol Rep
, vol.2
, pp. 51
-
-
Lemon, R.N.1
-
46
-
-
0344872757
-
Direct and indirect pathways for corticospinal control of upper limb motoneurons in the primate
-
PID: 14653171
-
Lemon RN, Kirkwood PA, Maier MA, Nakajima K, Nathan P (2004) Direct and indirect pathways for corticospinal control of upper limb motoneurons in the primate. Prog Brain Res 143:263–279
-
(2004)
Prog Brain Res
, vol.143
, pp. 263-279
-
-
Lemon, R.N.1
Kirkwood, P.A.2
Maier, M.A.3
Nakajima, K.4
Nathan, P.5
-
48
-
-
84945119424
-
A revision of the El Escorial criteria––2015
-
PID: 26121170
-
Ludolph A, Drory V, Hardiman O, Nakano I, Ravits J, Robberecht W et al (2015) A revision of the El Escorial criteria––2015. Amyotroph Lateral Scler Frontotemporal Degener 16:291–292
-
(2015)
Amyotroph Lateral Scler Frontotemporal Degener
, vol.16
, pp. 291-292
-
-
Ludolph, A.1
Drory, V.2
Hardiman, O.3
Nakano, I.4
Ravits, J.5
Robberecht, W.6
-
49
-
-
34249946466
-
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations
-
COI: 1:CAS:528:DC%2BD2sXnsFKmtbc%3D, PID: 17469116
-
Mackenzie IR, Bigio EH, Ince PG, Geser F, Neumann M, Cairns N et al (2007) Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations. Ann Neurol 61:427–434
-
(2007)
Ann Neurol
, vol.61
, pp. 427-434
-
-
Mackenzie, I.R.1
Bigio, E.H.2
Ince, P.G.3
Geser, F.4
Neumann, M.5
Cairns, N.6
-
50
-
-
84938740314
-
From nucleation to widespread propagation: a prion-like concept for ALS
-
Maniecka Z, Polymenidou M (2015) From nucleation to widespread propagation: a prion-like concept for ALS. Virus Res 2:94–105
-
(2015)
Virus Res
, vol.2
, pp. 94-105
-
-
Maniecka, Z.1
Polymenidou, M.2
-
51
-
-
85015606615
-
Nuclear trafficking in amyotrophic lateral sclerosis and frontotemporal lobar degeneration
-
Mihevc SP, Darovic S, Kovanda A, Česnik AB, Župunski V, Rogelj B (2016) Nuclear trafficking in amyotrophic lateral sclerosis and frontotemporal lobar degeneration. Brain. doi:10.1093/brain/aww1971-14
-
(2016)
Brain
-
-
Mihevc, S.P.1
Darovic, S.2
Kovanda, A.3
Česnik, A.B.4
Župunski, V.5
Rogelj, B.6
-
52
-
-
47949099336
-
Maturation process of TDP-43-positive neuronal cytoplasmic inclusions in amyotrophic lateral sclerosis with and without dementia
-
COI: 1:CAS:528:DC%2BD1cXosVyisb4%3D, PID: 18560845
-
Mori F, Tanji K, Zhang HX, Hishihara Y, Tan CF, Takahashi H et al (2008) Maturation process of TDP-43-positive neuronal cytoplasmic inclusions in amyotrophic lateral sclerosis with and without dementia. Acta Neuropathol 116:193–203
-
(2008)
Acta Neuropathol
, vol.116
, pp. 193-203
-
-
Mori, F.1
Tanji, K.2
Zhang, H.X.3
Hishihara, Y.4
Tan, C.F.5
Takahashi, H.6
-
53
-
-
84974588587
-
A large-scale multicentre cerebral diffusion tensor imaging study in amyotrophic lateral sclerosis
-
PID: 26746186
-
Müller HP, Turner MR, Grosskreutz J, Abrahmas S, Bede P, Govind V et al (2016) A large-scale multicentre cerebral diffusion tensor imaging study in amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry 87:570–579
-
(2016)
J Neurol Neurosurg Psychiatry
, vol.87
, pp. 570-579
-
-
Müller, H.P.1
Turner, M.R.2
Grosskreutz, J.3
Abrahmas, S.4
Bede, P.5
Govind, V.6
-
54
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
COI: 1:CAS:528:DC%2BD28XhtVCiurrL, PID: 17023659
-
Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, Chou TT 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
-
55
-
-
59249085091
-
Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies
-
COI: 1:CAS:528:DC%2BD1MXhtVCltLw%3D, PID: 19125255
-
Neumann M, Kwong LK, Lee EB, Kremmer E, Flatley A, Xu Y et al (2009) Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies. Acta Neuropathol 117:137–149
-
(2009)
Acta Neuropathol
, vol.117
, pp. 137-149
-
-
Neumann, M.1
Kwong, L.K.2
Lee, E.B.3
Kremmer, E.4
Flatley, A.5
Xu, Y.6
-
56
-
-
0027213817
-
Patterns of neuronal degeneration in the motor cortex of amyotrophic lateral sclerosis
-
COI: 1:STN:280:DyaK3szotlKmtw%3D%3D, PID: 8396837
-
Nihei K, McKee AC, Kowall NW (1993) Patterns of neuronal degeneration in the motor cortex of amyotrophic lateral sclerosis. Acta Neuropathol 86:55–64
-
(1993)
Acta Neuropathol
, vol.86
, pp. 55-64
-
-
Nihei, K.1
McKee, A.C.2
Kowall, N.W.3
-
57
-
-
57049139889
-
Sporadic amyotrophic lateral sclerosis of long duration is associated with relatively mild TDP-43 pathology
-
COI: 1:CAS:528:DC%2BD1cXhsVeksrfJ, PID: 18923836
-
Nishihira Y, Tan CF, Hoshi Y, Iwanaga K, Yamada M, Kawachi I et al (2009) Sporadic amyotrophic lateral sclerosis of long duration is associated with relatively mild TDP-43 pathology. Acta Neuropathol 117:45–53
-
(2009)
Acta Neuropathol
, vol.117
, pp. 45-53
-
-
Nishihira, Y.1
Tan, C.F.2
Hoshi, Y.3
Iwanaga, K.4
Yamada, M.5
Kawachi, I.6
-
58
-
-
0027264051
-
Oculomotor nuclear pathology in amyotrophic lateral sclerosis
-
COI: 1:STN:280:DyaK3s3mt12gug%3D%3D, PID: 8493857
-
Okamoto K, Hirai S, Amari M, Iizuka T, Watanabe M, Murakami N et al (1993) Oculomotor nuclear pathology in amyotrophic lateral sclerosis. Acta Neuropathol 85:458–462
-
(1993)
Acta Neuropathol
, vol.85
, pp. 458-462
-
-
Okamoto, K.1
Hirai, S.2
Amari, M.3
Iizuka, T.4
Watanabe, M.5
Murakami, N.6
-
59
-
-
84928660143
-
Cell to cell spreading of misfolded proteins as a therapeutic target in motor neuron disease
-
COI: 1:CAS:528:DC%2BC2cXhs1Gmtb3I, PID: 24934358
-
Pasquali L, Lenzi P, Biagioni F, Siciliano G, Fornai F (2014) Cell to cell spreading of misfolded proteins as a therapeutic target in motor neuron disease. Curr Med Chem 21:3508–3534
-
(2014)
Curr Med Chem
, vol.21
, pp. 3508-3534
-
-
Pasquali, L.1
Lenzi, P.2
Biagioni, F.3
Siciliano, G.4
Fornai, F.5
-
60
-
-
0037251889
-
Neuropathology with clinical correlations of sporadic amyotrophic lateral sclerosis: 102 autopsy cases examined between 1962 and 2000
-
PID: 12580541
-
Piao YS, Wakabayashi K, Kakita A, Yamada M, Hayashi S, Morita T et al (2003) Neuropathology with clinical correlations of sporadic amyotrophic lateral sclerosis: 102 autopsy cases examined between 1962 and 2000. Brain Pathol 13:10–22
-
(2003)
Brain Pathol
, vol.13
, pp. 10-22
-
-
Piao, Y.S.1
Wakabayashi, K.2
Kakita, A.3
Yamada, M.4
Hayashi, S.5
Morita, T.6
-
61
-
-
74049138727
-
The effect of prolonged fixation time on immunohistochemical staining of common neurodegenerative disease markers
-
COI: 1:CAS:528:DC%2BC3cXjs1Wq, PID: 20010304
-
Pikkarainen M, Martikainen P, Alafuzoff I (2010) The effect of prolonged fixation time on immunohistochemical staining of common neurodegenerative disease markers. J Neuropathol Exp Neurol 69:40–52
-
(2010)
J Neuropathol Exp Neurol
, vol.69
, pp. 40-52
-
-
Pikkarainen, M.1
Martikainen, P.2
Alafuzoff, I.3
-
62
-
-
84863808563
-
Prion-like spread of protein aggregates in neurodegeneration
-
COI: 1:CAS:528:DC%2BC38Xmsl2itLw%3D, PID: 22566400
-
Polymenidou M, Cleveland DW (2012) Prion-like spread of protein aggregates in neurodegeneration. J Exp Med 209:889–893
-
(2012)
J Exp Med
, vol.209
, pp. 889-893
-
-
Polymenidou, M.1
Cleveland, D.W.2
-
63
-
-
58849084705
-
Subdivisions of primary motor cortex based on cortico-motoneuronal cells
-
COI: 1:CAS:528:DC%2BD1MXht1yqt7w%3D, PID: 19139417
-
Rathelot JA, Strick PL (2009) Subdivisions of primary motor cortex based on cortico-motoneuronal cells. PNAS 106:918–923
-
(2009)
PNAS
, vol.106
, pp. 918-923
-
-
Rathelot, J.A.1
Strick, P.L.2
-
64
-
-
84981188324
-
Physiological functions and pathobiology of TDP-43 and FUS/TLS proteins
-
COI: 1:CAS:528:DC%2BC28XpvFChsbs%3D, PID: 27015757
-
Ratti A, Buratti E (2016) Physiological functions and pathobiology of TDP-43 and FUS/TLS proteins. J Neurochem 138(Suppl 1):95–111
-
(2016)
J Neurochem
, vol.138
, pp. 95-111
-
-
Ratti, A.1
Buratti, E.2
-
65
-
-
70349581626
-
ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration
-
PID: 19738176
-
Ravits JM, La Spada AR (2009) ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration. Neurology 73:805–811
-
(2009)
Neurology
, vol.73
, pp. 805-811
-
-
Ravits, J.M.1
La Spada, A.R.2
-
66
-
-
84945953187
-
Neuropathology of amyotrophic lateral sclerosis and its variants
-
PID: 26515626
-
Saberi S, Stauffer JE, Schulte DJ, Ravits J (2015) Neuropathology of amyotrophic lateral sclerosis and its variants. Neurol Clin 33:855–876
-
(2015)
Neurol Clin
, vol.33
, pp. 855-876
-
-
Saberi, S.1
Stauffer, J.E.2
Schulte, D.J.3
Ravits, J.4
-
67
-
-
84943617397
-
Simulating disease propagation across white matter connectome reveals anatomical substrate for neuropathology staging in amyotrophic lateral sclerosis
-
PID: 25869856
-
Schmidt R, de Reus MA, Scholtens LH, van den Berg LH, van den Heuvel MP (2016) Simulating disease propagation across white matter connectome reveals anatomical substrate for neuropathology staging in amyotrophic lateral sclerosis. NeuroImage 124:762–769
-
(2016)
NeuroImage
, vol.124
, pp. 762-769
-
-
Schmidt, R.1
de Reus, M.A.2
Scholtens, L.H.3
van den Berg, L.H.4
van den Heuvel, M.P.5
-
68
-
-
79960177202
-
Oculomotor dysfunction in amyotrophic lateral sclerosis: a comprehensive review
-
PID: 21747027
-
Sharma R, Hicks S, Berna CM, Kennard C, Talbot K, Turner MR (2011) Oculomotor dysfunction in amyotrophic lateral sclerosis: a comprehensive review. Arch Neurol 68:857–861
-
(2011)
Arch Neurol
, vol.68
, pp. 857-861
-
-
Sharma, R.1
Hicks, S.2
Berna, C.M.3
Kennard, C.4
Talbot, K.5
Turner, M.R.6
-
69
-
-
84949096416
-
Review: prion-like mechanisms of transactive response DNA binding protein of 43 kDa (TDP-43) in amyotrophic lateral sclerosis (ALS)
-
COI: 1:CAS:528:DC%2BC2MXht1SrsbnP, PID: 25487060
-
Smethurst P, Sidle KCL, Hardy J (2015) Review: prion-like mechanisms of transactive response DNA binding protein of 43 kDa (TDP-43) in amyotrophic lateral sclerosis (ALS). Neuropathol Appl Neurobiol 41:578–597
-
(2015)
Neuropathol Appl Neurobiol
, vol.41
, pp. 578-597
-
-
Smethurst, P.1
Sidle, K.C.L.2
Hardy, J.3
-
70
-
-
85005917048
-
Classification of FTLD-TDP cases into pathological subtypes using antibodies against phosphorylated and non-phosphorylated TDP43
-
COI: 1:CAS:528:DC%2BC2MXptVSqug%3D%3D, PID: 24252630
-
Tan RH, Shepherd CE, Kril JJ, McCann H, McGeachie A, McGinley C et al (2013) Classification of FTLD-TDP cases into pathological subtypes using antibodies against phosphorylated and non-phosphorylated TDP43. Acta Neuropathol Commun 1:33
-
(2013)
Acta Neuropathol Commun
, vol.1
, pp. 33
-
-
Tan, R.H.1
Shepherd, C.E.2
Kril, J.J.3
McCann, H.4
McGeachie, A.5
McGinley, C.6
-
71
-
-
0037172826
-
Phases of Aβ-deposition in the human brain and its relevance for the development of AD
-
PID: 12084879
-
Thal DR, Rüb U, Orantes M, Braak H (2002) Phases of Aβ-deposition in the human brain and its relevance for the development of AD. Neurology 58:1791–1800
-
(2002)
Neurology
, vol.58
, pp. 1791-1800
-
-
Thal, D.R.1
Rüb, U.2
Orantes, M.3
Braak, H.4
-
72
-
-
84867064451
-
Extrasynaptic exocytosis and its mechanisms: a source of molecular mediating volume transmission in the nervous system
-
PID: 22969726
-
Trueta C, De-Miguel FF (2012) Extrasynaptic exocytosis and its mechanisms: a source of molecular mediating volume transmission in the nervous system. Front Physiol 3:319
-
(2012)
Front Physiol
, vol.3
, pp. 319
-
-
Trueta, C.1
De-Miguel, F.F.2
-
73
-
-
36949008994
-
TDP-43 immunoreactive neuronal and glial inclusions in the neostriatum in amyotrophic lateral sclerosis with and without dementia
-
COI: 1:CAS:528:DC%2BD2sXhtlOqtrnK, PID: 17786458
-
Zhang H, Tan CF, Mori F et al (2008) TDP-43 immunoreactive neuronal and glial inclusions in the neostriatum in amyotrophic lateral sclerosis with and without dementia. Acta Neuropathol 115:115–122
-
(2008)
Acta Neuropathol
, vol.115
, pp. 115-122
-
-
Zhang, H.1
Tan, C.F.2
Mori, F.3
|