-
1
-
-
0036160338
-
Frontotemporal dementia
-
Snowden, J.S.; Neary, D.; Mann, D.M. Frontotemporal dementia. Br. J. Psychiatry., 2002, 180, 140-143
-
(2002)
Br. J. Psychiatry
, vol.180
, pp. 140-143
-
-
Snowden, J.S.1
Neary, D.2
Mann, D.M.3
-
2
-
-
33751001753
-
Progression in frontotemporal dementia: Identifying a benign behavioral variant by magnetic resonance imaging
-
Davies, R.R.; Kipps, C.M.; Mitchell, J.; Kril, J.J.; Halliday, G.M.; Hodges, J.R. Progression in frontotemporal dementia: identifying a benign behavioral variant by magnetic resonance imaging. Arch. Neurol., 2006, 63(11),1627-1631
-
(2006)
Arch. Neurol.
, vol.63
, Issue.11
, pp. 1627-1631
-
-
Davies, R.R.1
Kipps, C.M.2
Mitchell, J.3
Kril, J.J.4
Halliday, G.M.5
Hodges, J.R.6
-
3
-
-
0037062609
-
The prevalence of frontotemporal dementia
-
Ratnavalli, E.; Brayne, C.; Dawson, K.; Hodges, J.R. The prevalence of frontotemporal dementia. Neurology, 2002, 58, 1615-1621
-
(2002)
Neurology
, vol.58
, pp. 1615-1621
-
-
Ratnavalli, E.1
Brayne, C.2
Dawson, K.3
Hodges, J.R.4
-
4
-
-
0037804089
-
The prevalence of frontal variant frontotemporal dementia and the frontal lobe syndrome in a population based sample of 85 year olds
-
DOI 10.1136/jnnp.74.7.867
-
Gislason, T.B.; Sjögren, M.; Larsson, L.; Skoog, I. The prevalence of frontal variant frontotemporal dementia and the frontal lobe syndrome in a population based sample of 85 year olds. J. Neurol. Neurosurg. Psychiatry, 2003, 74, 867-871 (Pubitemid 36782985)
-
(2003)
Journal of Neurology Neurosurgery and Psychiatry
, vol.74
, Issue.7
, pp. 867-871
-
-
Gislason, T.B.1
Sjogren, M.2
Larsson, L.3
Skoog, I.4
-
5
-
-
0041320789
-
Frontotemporal dementia in the Netherlands: Patient characteristics and prevalence estimates from a population-based study
-
Rosso, S.M.; Donker Kaat, L.; Baks, T.; Joosse, M.; de Koning, I.; Pijnenburg, Y.; de Jong, D.; Dooijes, D.; Kamphorst, W.; Ravid, R.; Niermeijer, M.F.; Verheij, F.; Kremer, H.P.; Scheltens, P.; van Duijn, C.M.; Heutink, P.; van Swieten, J.C. Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study. Brain, 2003, 126, 2016-2022
-
(2003)
Brain
, vol.126
, pp. 2016-2022
-
-
Rosso, S.M.1
Donker Kaat, L.2
Baks, T.3
Joosse, M.4
De Koning, I.5
Pijnenburg, Y.6
De Jong, D.7
Dooijes, D.8
Kamphorst, W.9
Ravid, R.10
Niermeijer, M.F.11
Verheij, F.12
Kremer, H.P.13
Scheltens, P.14
Van Duijn, C.M.15
Heutink, P.16
Van Swieten, J.C.17
-
6
-
-
0031672540
-
Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria
-
Neary, D.; Snowden, J.S.; Gustafson, L.; Passant, U.; Stuss, D.; Black, S.; Freedman, M.; Kertesz, A.; Robert, P.H.; Albert, M.; Boone, K.; Miller, B.L.; Cummings, J.; Benson, D.F. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology, 1998, 51(6), 1546-1554 (Pubitemid 28565230)
-
(1998)
Neurology
, vol.51
, Issue.6
, pp. 1546-1554
-
-
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
Boone, K.11
Miller, B.L.12
Cummings, J.13
Benson, D.F.14
-
7
-
-
0034764622
-
Clinical and pathological diagnosis of frontotemporal dementia: Report of the Work Group on Frontotemporal Dementia and Pick's Disease
-
WorkGroup on Frontotemporal Dementia and Pick's Disease
-
McKhann, G.M.; Albert, M.S.; Grossman, M.; Miller, B.; Dickson, D.; Trojanowski, J.Q.; WorkGroup on Frontotemporal Dementia and Pick's Disease. Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease. Arch. Neurol., 2001, 58, 1803-1809
-
(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
-
8
-
-
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, 1077-1079.
-
(2002)
Neurology
, vol.59
, pp. 1077-1079
-
-
Lomen-Hoerth, C.1
Anderson, T.2
Miller, B.3
-
9
-
-
0037933417
-
Preferred Terminology
-
Kertesz, A.; Munoz, D.G.; Hillis, A. Preferred Terminology. Ann. Neurol., 2003, 54(Suppl 5), S3-S6.
-
(2003)
Ann. Neurol.
, vol.54
, Issue.SUPPL. 5
-
-
Kertesz, A.1
Munoz, D.G.2
Hillis, A.3
-
10
-
-
34447096691
-
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: Consensus of the Consortium for Frontotemporal Lobar Degeneration
-
Consortium for Frontotemporal Lobar Degeneration
-
Cairns, N.J.; Bigio, E.H.; Mackenzie, I.R.; Neumann, M.; Lee, V.M.; Hatanpaa, K.J.; White, C.L. 3rd; Schneider, J.A.; Grinberg, L.T.; Halliday, G.; Duyckaerts, C.; Lowe, J.S.; Holm, I.E.; Tolnay, M.; Okamoto, K.; Yokoo, H.; Murayama, S.; Woulfe, J.; Munoz, D.G.; Dickson, D.W.; Ince, P.G.; Trojanowski, J.Q.; Mann, D.M.; Consortium for Frontotemporal Lobar Degeneration. Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration. Acta Neuropathol. (Berl), 2007, 114, 5-22.
-
(2007)
Acta Neuropathol. (Berl)
, vol.114
, pp. 5-22
-
-
Cairns, N.J.1
Bigio, E.H.2
Mackenzie, I.R.3
Neumann, M.4
Lee, V.M.5
Hatanpaa, K.J.6
White III, C.L.7
Schneider, J.A.8
Grinberg, L.T.9
Halliday, G.10
Duyckaerts, C.11
Lowe, J.S.12
Holm, I.E.13
Tolnay, M.14
Okamoto, K.15
Yokoo, H.16
Murayama, S.17
Woulfe, J.18
Munoz, D.G.19
Dickson, D.W.20
Ince, P.G.21
Trojanowski, J.Q.22
Mann, D.M.23
more..
-
11
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
DOI 10.1126/science.1134108
-
Neumann, M.; Sampathu, D.M.; Kwong, L.K.; Truax, A.C.; Micsenyi, M.C.; Chou, T.T.; Bruce, J.; Schuck, T.; Grossman, M.; Clark, C. M.; McCluskey, L. F.; Miller, B. L.; Masliah, E.; Mackenzie, I. R.; Feldman, H.; Feiden, W.; Kretzschmar, H. A.; Trojanowski, J. Q.; Lee, V. M.-Y. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science, 2006, 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
-
12
-
-
0031800415
-
Familial aggregation in frontotemporal dementia
-
Stevens, M.; van Duijn, C.M.; Kamphorst, W.; de Knijff, P.; Heutink, P.; van Gool, W.A.; Scheltens, P.; Ravid, R.; Oostra, B.A.; Niermeijer, M.F.; van Swieten, J.C. Familial aggregation in frontotemporal dementia. Neurology, 1998, 50, 1541-1545
-
(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
Scheltens, P.7
Ravid, R.8
Oostra, B.A.9
Niermeijer, M.F.10
Van Swieten, J.C.11
-
13
-
-
0029119112
-
Familial non-specific dementia maps to chromosome 3
-
Brown, J.; Ashworth, A.; Gydesen, S.; Sorensen, A.; Rossor, M.; Hardy, J.; Collinge, J. Familial non-specific dementia maps to chromosome 3. Hum. Mol. Genet., 1995, 4, 1625-1628
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1625-1628
-
-
Brown, J.1
Ashworth, A.2
Gydesen, S.3
Sorensen, A.4
Rossor, M.5
Hardy, J.6
Collinge, J.7
-
14
-
-
0034605478
-
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22
-
Hosler, B.A.; Siddique, T.; Sapp, P.C.; Sailor, W.; Huang, M.C.; Hossain, A.; Daube, J.R.; Nance, M.; Fan, C.; Kaplan, J.; Hung, W.Y.; McKenna-Yasek, D.; Haines, J.L.; Pericak-Vance, M.A.; Horvitz, H.R.; Brown, R.H. Jr. Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22. JAMA, 2000, 284(13), 1664-1669
-
(2000)
JAMA
, vol.284
, Issue.13
, pp. 1664-1669
-
-
Hosler, B.A.1
Siddique, T.2
Sapp, P.C.3
Sailor, W.4
Huang, M.C.5
Hossain, A.6
Daube, J.R.7
Nance, M.8
Fan, C.9
Kaplan, J.10
Hung, W.Y.11
McKenna-Yasek, D.12
Haines, J.L.13
Pericak-Vance, M.A.14
Horvitz, H.R.15
Brown Jr., R.H.16
-
15
-
-
33645062075
-
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia
-
Morita, M.; Al-Chalabi, A.; Andersen, P.M.; Hosler, B.; Sapp, P.; Englund, E.; Mitchell, J.E.; Habgood, J.J.; de Belleroche, J.; Xi, J.; Jongjaroenprasert, W.; Horvitz H.R.; Gunnarsson, L.G.; Brown, R.H. Jr. A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia. Neurology, 2006, 66(6), 839-844
-
(2006)
Neurology
, vol.66
, Issue.6
, pp. 839-844
-
-
Morita, M.1
Al-Chalabi, A.2
Andersen, P.M.3
Hosler, B.4
Sapp, P.5
Englund, E.6
Mitchell, J.E.7
Habgood, J.J.8
De Belleroche, J.9
Xi, J.10
Jongjaroenprasert, W.11
Horvitz, H.R.12
Gunnarsson, L.G.13
Brown Jr., R.H.14
-
16
-
-
33645069660
-
Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3
-
Vance, C.; Al-Chalabi, A.; Ruddy, D.; Smith, B.N.; Hu, X.; Sreedharan, J.; Siddique, T.; Schelhaas, H.J.; Kusters, B.; Troost, D.; Baas, F.; de Jong, V.; Shaw, C.E. Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3. Brain, 2006,129, 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
Baas, F.11
De Jong, V.12
Shaw, C.E.13
-
17
-
-
0032543684
-
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17
-
DOI 10.1038/31508
-
Hutton, M.; Lendon, C.; Rizzu, P.; Baker, M.; Froelich, S.; Houlden, H.; Pickering-Brown, S.; Chakraverty, S.; Isaacs, A.; Grover, A.; Hackett, J.; Adamson, J.; Lincoln, S.; Dickson, D.; Davies, P.; Petersen, R.C.; Stevens, M.; de Graaff, E.; Wauters, E.; van Baren, J.; Hillebrand, M.; Joosse, M.; Kwon, J.M.; Nowotny, P.; Che, L.K.; Norton, J.; Morris, J.C.; Reed L.A.; Trojanowski, J.; Basun, H.; Lannfelt, L.; Neystat, M.; Fahn, S.; Dark, F.; Tannenberg, T.; Dodd, P.R.; Hayward, N.; Kwok, J.B.; Schofield, P.R.; Andreadis, A.; Snowden, J.; Craufurd, D.; Neary, D.; Owen, F.; Oostra, B.A.; Hardy, J.; Goate, A.; van Swieten, J.; Mann, D.; Lynch, T.; Heutink, P. Association of missense and 59-splice-site mutations in tau with inherited dementia FTDP-17. Nature, 1998, 393,702-705. (Pubitemid 28289662)
-
(1998)
Nature
, vol.393
, Issue.6686
, pp. 702-704
-
-
Hutton, M.1
Lendon, C.L.2
Rizzu, P.3
Baker, M.4
Froelich, S.5
Houlden, H.H.6
Pickering-Brown, S.7
Chakraverty, S.8
Isaacs, A.9
Grover, A.10
Hackett, J.11
Adamson, J.12
Lincoln, S.13
Dickson, D.14
Davies, P.15
Petersen, R.C.16
Stevena, M.17
De Graaff, E.18
Wauters, E.19
Van Baren, J.20
Hillebrand, M.21
Joosse, M.22
Kwon, J.M.23
Nowotny, P.24
Che, L.K.25
Norton, J.26
Morris, J.C.27
Reed, L.A.28
Trojanowski, J.29
Basun, H.30
Lannfelt, L.31
Neystat, M.32
Fahn, S.33
Dark, F.34
Tannenberg, T.35
Dodd, P.R.36
Hayward, N.37
Kwok, J.B.J.38
Schofield, P.R.39
Andreadis, A.40
Snowden, J.41
Craufurd, D.42
Neary, D.43
Owen, F.44
Costra, B.A.45
Hardy, J.46
Goate, A.47
Van Swieten, J.48
Mann, D.49
Lynch, T.50
Heutink, P.51
more..
-
18
-
-
33847194237
-
Hereditary frontotemporal dementia caused by Tau gene mutations
-
DOI 10.1111/j.1750-3639.2007.00052.x
-
van Swieten, J.; Spillantini, M.G. Hereditary frontotemporal dementia caused by Tau gene mutations. Brain. Pathol., 2007, 17(1), 63-73. (Pubitemid 46310686)
-
(2007)
Brain Pathology
, vol.17
, Issue.1
, pp. 63-73
-
-
Van Swieten, J.1
Spillantini, M.G.2
-
19
-
-
23044471011
-
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
-
DOI 10.1038/ng1609
-
Skibinski, G.; Parkinson, N.J.; Brown, J.M.; Chakrabarti, L.; Lloyd, S.L.; Hummerich, H.; Nielsen, J.E.; Hodges, J.R.; Spillantini, M.G.; Thusgaard, T.; Brandner, S.; Brun, A.; Rossor, M.N.; Gade, A.; Johannsen, P.; Sørensen, S.A.; Gydesen, S.; Fisher, E.M.; Collinge, J. Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia. Nat. Genet., 2005, 37, 806-808. (Pubitemid 41077105)
-
(2005)
Nature Genetics
, vol.37
, Issue.8
, pp. 806-808
-
-
Skibinski, G.1
Parkinson, N.J.2
Brown, J.M.3
Chakrabarti, L.4
Lloyd, S.L.5
Hummerich, H.6
Nielsen, J.E.7
Hodges, J.R.8
Spillantini, M.G.9
Thusgaard, T.10
Brandner, S.11
Brun, A.12
Rossor, M.N.13
Gade, A.14
Johannsen, P.15
Sorensen, S.A.16
Gydesen, S.17
Fisher, E.M.C.18
Collinge, J.19
-
20
-
-
1842483843
-
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
-
Watts, G.D.; Wymer, J.; Kovach, M.J.; Mehta, S.G.; Mumm, S.; Darvish, D.; Pestronk, A.; Whyte, M.P.; Kimonis, V.E. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. Nat. Genet., 2004, 36: 377-381
-
(2004)
Nat. Genet.
, vol.36
, pp. 377-381
-
-
Watts, G.D.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
-
21
-
-
33746910649
-
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
-
DOI 10.1038/nature05017, PII NATURE05017
-
Cruts, M.; Gijselinck, I.; van der Zee, J.; Engelborghs, S.; Wils, H.; Pirici, D.; Rademakers, R.; Vandenberghe, R.; Dermaut, B.; Martin, J.J.; van Duijn, C.; Peeters, K.; Sciot, R.; Santens, P.; De Pooter, T.; Mattheijssens, M.; Van den Broeck, M.; Cuijt, I.; Vennekens, K.; De Deyn, P.P.; Kumar-Singh, S.; Van Broeckhoven, C. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature, 2006, 442, 920-924. (Pubitemid 44285947)
-
(2006)
Nature
, vol.442
, Issue.7105
, 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
Van Duijn, C.11
Peeters, K.12
Sciot, R.13
Santens, P.14
De Pooter, T.15
Mattheijssens, M.16
Van Den Broeck, M.17
Cuijt, I.18
Vennekens, K.19
De Deyn, P.P.20
Kumar-Singh, S.21
Van Broeckhoven, C.22
more..
-
22
-
-
33746919083
-
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
-
DOI 10.1038/nature05016, PII NATURE05016
-
Baker, M.; Mackenzie, I.R.; Pickering-Brown, S.M.; Gass, J.; Rademakers, R.; Lindholm, C.; Snowden, J.; Adamson, J.; Sadovnick, A.D.; Rollinson, S.; Cannon, A.; Dwosh, E.; Neary, D.; Melquist, S.; Richardson, A.; Dickson, D.; Berger, Z.; Eriksen, J.; Robinson, T.; Zehr, C.; Dickey, C.A.; Crook, R.; McGowan, E.; Mann, D.; Boeve, B.; Feldman, H.; Hutton, M. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature, 2006, 442, 916-919. (Pubitemid 44285946)
-
(2006)
Nature
, vol.442
, Issue.7105
, pp. 916-919
-
-
Baker, M.1
Mackenzie, 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
Cannon, A.11
Dwosh, E.12
Neary, D.13
Melquist, S.14
Richardson, A.15
Dickson, D.16
Berger, Z.17
Eriksen, J.18
Robinson, T.19
Zehr, C.20
Dickey, C.A.21
Crook, R.22
McGowan, E.23
Mann, D.24
Boeve, B.25
Feldman, H.26
Hutton, M.27
more..
-
23
-
-
42049087853
-
Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival
-
DOI 10.1083/jcb.200712039
-
Van Damme, P.; Van Hoecke, A.; Lambrechts, D.; Vanacker, P.; Bogaert, E.; van Swieten, J.; Carmeliet, P.; Van Den Bosch, L.; Robberecht, W. Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival. J. Cell Biol., 2008, 181(1), 37. (Pubitemid 351519762)
-
(2008)
Journal of Cell Biology
, vol.181
, Issue.1
, pp. 37-41
-
-
Van Damme, P.1
Van Hoecke, A.2
Lambrechts, D.3
Vanacker, P.4
Bogaert, E.5
Van Swieten, J.6
Carmeliet, P.7
Van Den Bosch, L.8
Robberecht, W.9
-
24
-
-
37349008891
-
Progranulin: Normal function and role in neurodegeneration
-
Eriksen, J.L.; Mackenzie, I.R. Progranulin: normal function and role in neurodegeneration. J. Neurochem., 2008, 104(2), 287-297
-
(2008)
J. Neurochem.
, vol.104
, Issue.2
, pp. 287-297
-
-
Eriksen, J.L.1
Mackenzie, I.R.2
-
25
-
-
42649120983
-
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
-
DOI 10.1038/ng.132, PII NG132
-
Kabashi, E.; Valdmanis, P.N.; Dion, P.; Spiegelman, D.; McConkey, B.J.; Vande Velde, C.; Bouchard, J.-P.; Lacomblez, L.; Pochigaeva, K.; Salachas, F.; Pradat, P.-F.; Camu, W.; Meininger, V.; Dupre, N.; Rouleau, G.A. TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nat. Genet., 2008, 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
-
26
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
DOI 10.1126/science.1154584
-
Sreedharan, J.; Blair, I.P.; Tripathi, V.B.; Hu, X.; Vance, C.; Rogelj, B.; Ackerley, S.; Durnall, J. C.; Williams, K. L.; Buratti, E.; Baralle, F.; de Belleroche, J.; Mitchell, J.D.; Leigh, P. N.; Al-Chalabi, A.; Miller, C.C.; Nicholson, G.; Shaw, C.E. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science, 2008, 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
-
27
-
-
47549085411
-
TDP-43 in neurodegenerative disorders
-
Cook, C.; Zhang, Y.J.; Xu, Y.F.; Dickson, D.W.; Petrucelli, L. TDP-43 in neurodegenerative disorders. Expert. Opin. Biol. Ther., 2008, 8, 969-978
-
(2008)
Expert. Opin. Biol. Ther.
, vol.8
, pp. 969-978
-
-
Cook, C.1
Zhang, Y.J.2
Xu, Y.F.3
Dickson, D.W.4
Petrucelli, L.5
-
28
-
-
36949038732
-
TDP-43 immunoreactivity in neurodegenerative disorders: Disease versus mechanism specificity
-
Dickson, D.W. TDP-43 immunoreactivity in neurodegenerative disorders: disease versus mechanism specificity. Acta Neuropathol., 2008, 115, 147-149.
-
(2008)
Acta Neuropathol.
, vol.115
, pp. 147-149
-
-
Dickson, D.W.1
-
29
-
-
52949094629
-
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis
-
Rutherford, N.J.; Zhang, Y.J.; Baker, M.; Gass, J.M.; Finch, N.A.; Xu, Y.F.; Stewart, H.; Kelley, B.J.; Kuntz, K.; Crook, R.J.; Sreedharan, J.; Vance, C.; Sorenson, E.; Lippa, C.; Bigio, E.H.; Geschwind, D.H.; Knopman, D.S.; Mitsumoto, H.; Petersen, R.C.; Cashman, NR.; Hutton, M.; Shaw, C.E.; Boylan, K.B.; Boeve, B.; Graff-Radford, N.R.; Wszolek, Z.K.; Caselli, R.J.; Dickson, D.W.; Mackenzie, I.R.; Petrucelli, L.; Rademakers, R. Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis. PLoS Genet., 2008, 4, e1000193.
-
(2008)
PLoS Genet.
, vol.4
-
-
Rutherford, N.J.1
Zhang, Y.J.2
Baker, M.3
Gass, J.M.4
Finch, N.A.5
Xu, Y.F.6
Stewart, H.7
Kelley, B.J.8
Kuntz, K.9
Crook, R.J.10
Sreedharan, J.11
Vance, C.12
Sorenson, E.13
Lippa, C.14
Bigio, E.H.15
Geschwind, D.H.16
Knopman, D.S.17
Mitsumoto, H.18
Petersen, R.C.19
Cashman, N.R.20
Hutton, M.21
Shaw, C.E.22
Boylan, K.B.23
Boeve, B.24
Graff-Radford, N.R.25
Wszolek, Z.K.26
Caselli, R.J.27
Dickson, D.W.28
Mackenzie, I.R.29
Petrucelli, L.30
Rademakers, R.31
more..
-
30
-
-
70350572209
-
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea
-
Kovacs, G.G.; Murrell, J.R.; Horvath, S.; Haraszti, L.; Majtenyi, K.; Molnar, M.J.; Budka, H., Ghetti, B.; Spina, S. TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea. Mov. Disord., 2009, 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
-
31
-
-
70350721803
-
Mutation within TARDBP leads to frontotemporal dementia without motor neuron disease
-
Borroni, B.; Bonvicini, C.; Alberici, A.; Buratti, E.; Agosti, C.; Archetti, S.; Papetti, A.; Stuani, C.; Di Luca, M.; Gennarelli, M.; Padovani, A. Mutation within TARDBP leads to frontotemporal dementia without motor neuron disease. Hum. Mutat., 2009, E974-983.
-
(2009)
Hum. Mutat.
-
-
Borroni, B.1
Bonvicini, C.2
Alberici, A.3
Buratti, E.4
Agosti, C.5
Archetti, S.6
Papetti, A.7
Stuani, C.8
Di Luca, M.9
Gennarelli, M.10
Padovani, A.11
-
32
-
-
61349162349
-
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
-
Vance, C.; Rogelj, B.; Hortobágyi, T.; De Vos, K.J.; Nishimura, A.L.; Sreedharan, J.; Hu, X.; Smith, B.; Ruddy, D.; Wright, P.; Ganesalingam, J.; Williams, K.L.; Tripathi, V.; Al-Saraj, S.; Al-Chalabi, A.; Leigh, P.N.; Blair, I.P.; Nicholson, G.; de Belleroche, J.; Gallo, J.M.; Miller, C.C.; Shaw, C.E. Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science, 2009, 323, 1208-1211.
-
(2009)
Science
, vol.323
, pp. 1208-1211
-
-
Vance, C.1
Rogelj, B.2
Hortobágyi, T.3
De Vos, K.J.4
Nishimura, A.L.5
Sreedharan, J.6
Hu, X.7
Smith, B.8
Ruddy, D.9
Wright, P.10
Ganesalingam, J.11
Williams, K.L.12
Tripathi, V.13
Al-Saraj, S.14
Al-Chalabi, A.15
Leigh, P.N.16
Blair, I.P.17
Nicholson, G.18
De Belleroche, J.19
Gallo, J.M.20
Miller, C.C.21
Shaw, C.E.22
more..
-
33
-
-
70350673956
-
A new subtype of frontotemporal lobar degeneration with FUS pathology
-
Neumann, M., Rademakers, R., Roeber, S., Baker, M., Kretzschmar, H.A., Mackenzie, I.R. A new subtype of frontotemporal lobar degeneration with FUS pathology. Brain, 2009, 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
Mackenzie, I.R.6
-
34
-
-
54449085260
-
Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration
-
Ghidoni, R.; Benussi, L.; Glionna, M.; Franzoni, M.; Binetti, G. Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration. Neurology, 2008, 71(16), 1235-1239
-
(2008)
Neurology
, vol.71
, Issue.16
, pp. 1235-1239
-
-
Ghidoni, R.1
Benussi, L.2
Glionna, M.3
Franzoni, M.4
Binetti, G.5
-
35
-
-
64849103956
-
Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members
-
Finch, N.; Baker, M.; Crook, R.; Swanson, K.; Kuntz, K.; Surtees, R.; Bisceglio, G.; Rovelet-Lecrux, A.; Boeve, B.; Petersen, R.C.; Dickson, D.W.; Younkin, S.G.; Deramecourt, V.; Crook, J.; Graff-Radford, N.R.; Rademakers, R. Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members. Brain, 2009, 132(Pt 3), 583-591
-
(2009)
Brain
, vol.132
, Issue.PART 3
, pp. 583-591
-
-
Finch, N.1
Baker, M.2
Crook, R.3
Swanson, K.4
Kuntz, K.5
Surtees, R.6
Bisceglio, G.7
Rovelet-Lecrux, A.8
Boeve, B.9
Petersen, R.C.10
Dickson, D.W.11
Younkin, S.G.12
Deramecourt, V.13
Crook, J.14
Graff-Radford, N.R.15
Rademakers, R.16
-
36
-
-
67249111266
-
Serum biomarker for progranulin-associated frontotemporal lobar degeneration
-
Sleegers, K.; Brouwers, N.; Van Damme, P.; Engelborghs, S.; Gijselinck, I.; van der Zee, J.; Peeters, K.; Mattheijssens, M.; Cruts, M.; Vandenberghe, R.; De Deyn, P.P.; Robberecht, W.; Van Broeckhoven, C. Serum biomarker for progranulin-associated frontotemporal lobar degeneration. Ann. Neurol., 2009, 65(5), 603-609
-
(2009)
Ann. Neurol.
, vol.65
, Issue.5
, pp. 603-609
-
-
Sleegers, K.1
Brouwers, N.2
Van Damme, P.3
Engelborghs, S.4
Gijselinck, I.5
Van Der Zee, J.6
Peeters, K.7
Mattheijssens, M.8
Cruts, M.9
Vandenberghe, R.10
De Deyn, P.P.11
Robberecht, W.12
Van Broeckhoven, C.13
-
37
-
-
0031577298
-
Cerebrospinal fluid tau levels in neurodegenerative diseases with distinct tau-related pathology
-
DOI 10.1006/bbrc.1997.6908
-
Arai, H.; Morikawa, Y.; Higuchi, M.; Matsui, T.; Clark, C.M.; Miura, M.; Machida, N.; Lee, V.M.; Trojanowski, J.Q.; Sasaki, H. Cerebrospinal fluid tau levels in neurodegenerative diseases with distinct tau-related pathology. Biochem. Biophys. Res. Commun., 1997, 236(2), 262-264 (Pubitemid 27373280)
-
(1997)
Biochemical and Biophysical Research Communications
, vol.236
, Issue.2
, pp. 262-264
-
-
Arai, H.1
Morikawa, Y.-I.2
Higuchi, M.3
Matsui, T.4
Clark, C.M.5
Miura, M.6
Machida, N.7
Lee, V.M.-Y.8
Trojanowski, J.Q.9
Sasaki, H.10
-
38
-
-
0033534519
-
Increased tau in the cerebrospinal fluid of patients with frontotemporal dementia and Alzheimer's disease
-
DOI 10.1016/S0304-3940(98)00904-5, PII S0304394098009045
-
Green, A.J.; Harvey, R.J.; Thompson, E.J.; Rossor, M.N. Increased tau in the cerebrospinal fluid of patients with frontotemporal dementia and Alzheimer's disease. Neurosci. Lett., 1999, 259(2), 133-135 (Pubitemid 29064148)
-
(1999)
Neuroscience Letters
, vol.259
, Issue.2
, pp. 133-135
-
-
Green, A.J.E.1
Harvey, R.J.2
Thompson, E.J.3
Rossor, M.N.4
-
39
-
-
0037062351
-
Tau and Abeta42 protein in CSF of patients with frontotemporal degeneration
-
Riemenschneider, M.; Wagenpfeil, S.; Diehl, J.; Lautenschlager, N.; Theml, T.; Heldmann, B.; Drzezga, A.; Jahn, T.; Förstl, H.; Kurz, A. Tau and Abeta42 protein in CSF of patients with frontotemporal degeneration. Neurology, 2002, 58(11), 1622-1628 (Pubitemid 34602892)
-
(2002)
Neurology
, vol.58
, Issue.11
, pp. 1622-1628
-
-
Riemenschneider, M.1
Wagenpfeil, S.2
Diehl, J.3
Lautenschlager, N.4
Theml, T.5
Heldmann, B.6
Drzezga, A.7
Jahn, T.8
Forstl, H.9
Kurz, A.10
-
40
-
-
0032433590
-
Tau protein in cerebrospinal fluid: A new diagnostic and prognostic marker in Alzheimer disease?
-
Mecocci, P.; Cherubini, A.; Bregnocchi, M.; Chionne, F.; Cecchetti, R.; Lowenthal, D.T.; Senin, U. Tau protein in cerebrospinal fluid: a new diagnostic and prognostic marker in Alzheimer disease?. Alzheimer. Dis. Assoc. Disord., 1998, 12(3), 211-214 (Pubitemid 29154992)
-
(1998)
Alzheimer Disease and Associated Disorders
, vol.12
, Issue.3
, pp. 211-214
-
-
Mecocci, P.1
Cherubini, A.2
Bregnocchi, M.3
Chionne, F.4
Cecchetti, R.5
Lowenthal, D.T.6
Senin, U.7
-
41
-
-
20944439059
-
Cerebrospinal fluid profile in frontotemporal dementia and Alzheimer's disease
-
DOI 10.1002/ana.20477
-
Grossman, M.; Farmer, J.; Leight, S.; Work, M.; Moore, P.; Van Deerlin, V.; Pratico, D.; Clark, C.M.; Coslett, H.B.; Chatterjee, A.; Gee, J.; Trojanowski, J.Q.; Lee, VM. Cerebrospinal fluid profile in frontotemporal dementia and Alzheimer's disease. Ann. Neurol., 2005, 57(5), 721-729 (Pubitemid 40628861)
-
(2005)
Annals of Neurology
, vol.57
, Issue.5
, pp. 721-729
-
-
Grossman, M.1
Farmer, J.2
Leight, S.3
Work, M.4
Moore, P.5
Van Deerlin, V.6
Pratico, D.7
Clark, C.M.8
Coslett, H.B.9
Chatterjee, A.10
Gee, J.11
Trojanowski, J.Q.12
Lee, V.M.-Y.13
-
42
-
-
43249091150
-
Diagnostic value of CSF biomarker profile in frontotemporal lobar degeneration
-
DOI 10.1097/WAD.0b013e3181610fea, PII 0000209320080100000007
-
Kapaki, E.; Paraskevas, G.P.; Papageorgiou, S.G.; Bonakis, A.; Kalfakis, N.; Zalonis, I.; Vassilopoulos, D. Diagnostic value of CSF biomarker profile in frontotemporal lobar degeneration. Alzheimer Dis Assoc Disord., 2008, 22(1), 47-53. (Pubitemid 351651397)
-
(2008)
Alzheimer Disease and Associated Disorders
, vol.22
, Issue.1
, pp. 47-53
-
-
Kapaki, E.1
Paraskevas, G.P.2
Papageorgiou, S.G.3
Bonakis, A.4
Kalfakis, N.5
Zalonis, I.6
Vassilopoulos, D.7
-
43
-
-
4344580599
-
CSF tau and Abeta42 are not useful in the diagnosis of frontotemporal lobar degeneration
-
Pijnenburg, Y.A.; Schoonenboom, N.S.; Rosso, S.M.; Mulder, C.; Van Kamp, G.J.; Van Swieten, J.C.; Scheltens, P. CSF tau and Abeta42 are not useful in the diagnosis of frontotemporal lobar degeneration. Neurology, 2004, 62(9), 1649. (Pubitemid 38608224)
-
(2004)
Neurology
, vol.62
, Issue.9
, pp. 1649
-
-
Pijnenburg, Y.A.L.1
Schoonenboom, N.S.M.2
Rosso, S.M.3
Mulder, C.4
Van Kamp, G.J.5
Van Swieten, J.C.6
Scheltens, P.7
-
44
-
-
43249106998
-
CSF biomarkers in frontotemporal lobar degeneration with known pathology
-
DOI 10.1212/01.wnl.0000311445.21321.fc, PII 0000611420080506100015
-
Bian, H.; Van Swieten, J.C.; Leight, S.; Massimo, L.; Wood, E.; Forman, M.; Moore, P.; de Koning, I.; Clark, C.M.; Rosso, S.; Trojanowski, J.; Lee, V.M.; Grossman, M. CSF biomarkers in frontotemporal lobar degeneration with known pathology. Neurology, 2008, 70(19 Pt 2), 1827-1835 (Pubitemid 351653951)
-
(2008)
Neurology
, vol.70
, Issue.19 PART 2
, pp. 1827-1835
-
-
Bian, H.1
Van Swieten, J.C.2
Leight, S.3
Massimo, L.4
Wood, E.5
Forman, M.6
Moore, P.7
De Koning, I.8
Clark, C.M.9
Rosso, S.10
Trojanowski, J.11
Lee, V.M.-Y.12
Grossman, M.13
-
45
-
-
32344434409
-
CSF biomarkers in frontotemporal lobar degeneration: Relations with clinical characteristics, apolipoprotein e genotype, and neuroimaging
-
DOI 10.1136/jnnp.2005.066043
-
Pijnenburg, Y.A.; Schoonenboom, S.N.; Barkhof, F.; Knol, D.L.; Mulder, C.; Van Kamp, G.J.; Van Swieten, J.C.; Scheltens, P. CSF biomarkers in frontotemporal lobar degeneration: relations with clinical characteristics, apolipoprotein E genotype, and neuroimaging. J. Neurol. Neurosurg. Psychiatry, 2006, 77(2), 246-248 (Pubitemid 43220853)
-
(2006)
Journal of Neurology, Neurosurgery and Psychiatry
, vol.77
, Issue.2
, pp. 246-248
-
-
Pijnenburg, Y.A.L.1
Schoonenboom, S.N.M.2
Barkhof, F.3
Knol, D.L.4
Mulder, C.5
Van Kamp, G.J.6
Van Swieten, J.C.7
Scheltens, P.8
-
46
-
-
33746267000
-
Tau haplotype affects CSF Tau levels in frontotemporal dementia: Implication for diagnostic purposes [3]
-
DOI 10.1007/s00415-006-0052-z
-
Borroni, B.; Di Luca, M.; Padovani, A. Tau haplotype affects CSF Tau levels in frontotemporal dementia: implication for diagnostic purposes. J. Neurol., 2006, 253(7), 946. (Pubitemid 44100452)
-
(2006)
Journal of Neurology
, vol.253
, Issue.7
, pp. 946
-
-
Borroni, B.1
Di Luca, M.2
Padovani, A.3
-
47
-
-
36448997798
-
A novel panel of cerebrospinal fluid biomarkers for the differential diagnosis of Alzheimer's disease versus normal aging and frontotemporal dementia
-
DOI 10.1159/000110576
-
Simonsen, A.H.; McGuire, J.; Podust, V.N.; Hagnelius, N.O.; Nilsson, T.K.; Kapaki, E.; Vassilopoulos, D.; Waldemar, G. A novel panel of cerebrospinal fluid biomarkers for the differential diagnosis of Alzheimer's disease versus normal aging and frontotemporal dementia. Dement. Geriatr. Cogn. Disord., 2007, 24(6), 434-440 (Pubitemid 350175903)
-
(2007)
Dementia and Geriatric Cognitive Disorders
, vol.24
, Issue.6
, pp. 434-440
-
-
Simonsen, A.H.1
McGuire, J.2
Podust, V.N.3
Hagnelius, N.-O.4
Nilsson, T.K.5
Kapaki, E.6
Vassilopoulos, D.7
Waldemar, G.8
-
48
-
-
27744487547
-
Identification of CSF biomarkers for frontotemporal dementia using SELDI-TOF
-
DOI 10.1016/j.expneurol.2005.08.002, PII S0014488605002712
-
Rüetschi, U.; Zetterberg, H.; Podust, V.N.; Gottfries, J.; Li, S.; Hviid Simonsen, A.; McGuire, J.; Karlsson, M.; Rymo, L.; Davies, H.; Minthon, L.; Blennow, K. Identification of CSF biomarkers for frontotemporal dementia using SELDI-TOF. Exp. Neurol., 2005, 196(2), 273-281 (Pubitemid 41607815)
-
(2005)
Experimental Neurology
, vol.196
, Issue.2
, pp. 273-281
-
-
Ruetschi, U.1
Zetterberg, H.2
Podust, V.N.3
Gottfries, J.4
Li, S.5
Hviid Simonsen, A.6
McGuire, J.7
Karlsson, M.8
Rymo, L.9
Davies, H.10
Minthon, L.11
Blennow, K.12
-
49
-
-
34347272662
-
Validation of amyloid-beta peptides in CSF diagnosis of neurodegenerative dementias
-
DOI 10.1038/sj.mp.4001967, PII 4001967
-
Bibl, M.; Mollenhauer, B.; Lewczuk, P.; Esselmann, H.; Wolf, S.; Trenkwalder, C.; Otto, M.; Stiens, G.; Rüther, E.; Kornhuber, J.; Wiltfang, J. Validation of amyloid-beta peptides in CSF diagnosis of neurodegenerative dementias. Mol. Psychiatry, 2007, 12(7), 671-680 (Pubitemid 46998250)
-
(2007)
Molecular Psychiatry
, vol.12
, Issue.7
, pp. 671-680
-
-
Bibl, M.1
Mollenhauer, B.2
Lewczuk, P.3
Esselmann, H.4
Wolf, S.5
Trenkwalder, C.6
Otto, M.7
Stiens, G.8
Ruther, E.9
Kornhuber, J.10
Wiltfang, J.11
-
50
-
-
75549116708
-
Progressive Supranuclear Palsy. a heterogeneous degeneration involving the brain stem, basal ganglia and cerebellum with vertical gaze and pseudobulbar palsy, nuchal dystonia and dementia
-
Steele, J.C.; Richardson, J.C.; Olszewski, J. Progressive Supranuclear Palsy. A heterogeneous degeneration involving the brain stem, basal ganglia and cerebellum with vertical gaze and pseudobulbar palsy, nuchal dystonia and dementia. Arch. Neurol., 1964, 10, 333-359
-
(1964)
Arch. Neurol.
, vol.10
, pp. 333-359
-
-
Steele, J.C.1
Richardson, J.C.2
Olszewski, J.3
-
51
-
-
0031026460
-
Accuracy of the clinical diagnosis of corticobasal degeneration: A clinicopathologic study
-
Litvan, I.; Agid, Y.; Goetz, C.; Jankovic, J.; Wenning, G.K.; Brandel, J.P.; Lai, E.C.; Verny, M.; Ray-Chaudhuri, K.; McKee, A.; Jellinger, K.; Pearce, R.K.; Bartko, J.J. Accuracy of the clinical diagnosis of corticobasal degeneration: a clinicopathologic study. Neurology, 1997, 48(1), 119-125 (Pubitemid 27039529)
-
(1997)
Neurology
, vol.48
, Issue.1
, pp. 119-125
-
-
Litvan, I.1
Agid, Y.2
Goetz, C.3
Jankovic, J.4
Wenning, G.K.5
Brandel, J.P.6
Lai, E.C.7
Verny, M.8
Ray-Chaudhuri, K.9
McKee, A.10
Jellinger, K.11
Pearce, R.K.B.12
Bartko, J.J.13
-
52
-
-
1542360727
-
Accuracy of clinical diagnosis of progressive supranuclear palsy
-
DOI 10.1002/mds.10680
-
Osaki, Y.; Ben-Shlomo, Y.; Lees, A.J.; Daniel, S.E.; Colosimo, C.; Wenning, G.; Quinn, N. Accuracy of clinical diagnosis of progressive supranuclear palsy. Mov. Disord., 2004, 19(2), 181-189 (Pubitemid 38312700)
-
(2004)
Movement Disorders
, vol.19
, Issue.2
, pp. 181-189
-
-
Osaki, Y.1
Ben-Shlomo, Y.2
Lees, A.J.3
Daniel, S.E.4
Colosimo, C.5
Wenning, G.K.6
Quinn, N.7
-
53
-
-
0036209085
-
The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service
-
Hughes, A.J.; Daniel, S.E.; Ben-Shlomo, Y.; Lees, A.J. The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service. Brain, 2002, 125(Pt 4), 861-870
-
(2002)
Brain
, vol.125
, Issue.PART 4
, pp. 861-870
-
-
Hughes, A.J.1
Daniel, S.E.2
Ben-Shlomo, Y.3
Lees, A.J.4
-
54
-
-
0035862785
-
Diagnostic significance of tau protein in cerebrospinal fluid from patients with corticobasal degeneration or progressive supranuclear palsy
-
DOI 10.1016/S0022-510X(00)00480-9, PII S0022510X00004809
-
Urakami, K.; Wada, K.,; Arai, H.; Sasaki, H.; Kanai, M.; Shoji, M.; Ishizu, H.; Kashihara, K.; Yamamoto, M.; Tsuchiya-Ikemoto, K.; Morimatsu, M.; Takashima, H.; Nakagawa, M.; Kurokawa, K.; Maruyama, H.; Kaseda, Y.; Nakamura, S.; Hasegawa, K.; Oono, H.; Hikasa, C.; Ikeda, K.; Yamagata, K.; Wakutani, Y.; Takeshima, T.; Nakashima, K. Diagnostic significance of tau protein in cerebrospinal fluid from patients with corticobasal degeneration or progressive supranuclear palsy. J. Neurol. Sci., 2001, 183(1), 95-98 (Pubitemid 32141077)
-
(2001)
Journal of the Neurological Sciences
, vol.183
, Issue.1
, pp. 95-98
-
-
Urakami, K.1
Wada, K.2
Arai, H.3
Sasaki, H.4
Kanai, M.5
Shoji, M.6
Ishizu, H.7
Kashihara, K.8
Yamamoto, M.9
Tsuchiya-Ikemoto, K.10
Morimatsu, M.11
Takashima, H.12
Nakagawa, M.13
Kurokawa, K.14
Maruyama, H.15
Kaseda, Y.16
Nakamura, S.17
Hasegawa, K.18
Oono, H.19
Hikasa, C.20
Ikeda, K.21
Yamagata, K.22
Wakutani, Y.23
Takeshima, T.24
Nakashima, K.25
more..
-
55
-
-
0031909451
-
Increased CSF tau protein in corticobasal degeneration
-
DOI 10.1007/s004150050173
-
Mitani, K.; Furiya, Y.; Uchihara, T.; Ishii, K.; Yamanouchi, H.; Mizusawa, H.; Mori, H. Increased CSF tau protein in corticobasal degeneration. J. Neurol., 1998, 245(1), 44-46 (Pubitemid 28118860)
-
(1998)
Journal of Neurology
, vol.245
, Issue.1
, pp. 44-46
-
-
Mitani, K.1
Furiya, Y.2
Uchihara, T.3
Ishii, K.4
Yamanouchi, H.5
Mizusawa, H.6
Mori, H.7
-
56
-
-
25644432885
-
42 in cerebrospinal fluid of patients with progressive supranuclear palsy and corticobasal degeneration
-
DOI 10.1016/j.jns.2005.05.015, PII S0022510X0500198X
-
Noguchi, M.; Yoshita, M.; Matsumoto, Y.; Ono, K.; Iwasa, K.; Yamada, M. Decreased beta-amyloid peptide42 in cerebrospinal fluid of patients with progressive supranuclear palsy and corticobasal degeneration. J. Neurol. Sci., 2005, 237(1-2), 61-65 (Pubitemid 41384015)
-
(2005)
Journal of the Neurological Sciences
, vol.237
, Issue.1-2
, pp. 61-65
-
-
Noguchi, M.1
Yoshita, M.2
Matsumoto, Y.3
Ono, K.4
Iwasa, K.5
Yamada, M.6
-
57
-
-
24644488779
-
The diagnostic value of cerebrospinal fluid tau protein in dementing and nondementing neuropsychiatric disorders
-
DOI 10.1177/0891988705277549
-
Paraskevas, G.P.; Kapaki, E.; Liappas, I.; Theotoka, I.; Mamali, I.; Zournas, C.; Lykouras, L. The diagnostic value of cerebrospinal fluid tau protein in dementing and nondementing neuropsychiatric disorders. J. Geriatr. Psychiatry Neurol., 2005, 18(3), 163-173 (Pubitemid 41284967)
-
(2005)
Journal of Geriatric Psychiatry and Neurology
, vol.18
, Issue.3
, pp. 163-173
-
-
Paraskevas, G.P.1
Kapaki, E.2
Liappas, I.3
Theotoka, I.4
Mamali, I.5
Zournas, C.6
Lykouras, L.7
-
58
-
-
56049128135
-
Pattern of Tau forms in CSF is altered in progressive supranuclear palsy
-
Borroni, B.; Gardoni, F.; Parnetti, L.; Magno, L.; Malinverno, M.; Saggese, E.; Calabresi, P.; Spillantini, M.G.; Padovani, A.; Di Luca, M. Pattern of Tau forms in CSF is altered in progressive supranuclear palsy. Neurobiol. Aging., 2009, 30(1), 34-40.
-
(2009)
Neurobiol. Aging
, vol.30
, Issue.1
, pp. 34-40
-
-
Borroni, B.1
Gardoni, F.2
Parnetti, L.3
Magno, L.4
Malinverno, M.5
Saggese, E.6
Calabresi, P.7
Spillantini, M.G.8
Padovani, A.9
Di Luca, M.10
-
59
-
-
33846450238
-
SMI35 in cerebrospinal fluid supports the differential diagnosis of parkinsonian syndromes
-
DOI 10.1002/mds.21124
-
Brettschneider, J.; Petzold, A.; Süssmuth, S.D.; Landwehrmeyer, G.B.; Ludolph, A.C.; Kassubek, J.; Tumani, H. Neurofilament heavy-chain NfH(SMI35) in cerebrospinal fluid supports the differential diagnosis of Parkinsonian syndromes. Mov. Disord., 2006, 21(12), 2224-2227 (Pubitemid 46140444)
-
(2006)
Movement Disorders
, vol.21
, Issue.12
, pp. 2224-2227
-
-
Brettschneider, J.1
Petzold, A.2
Sussmuth, S.D.3
Landwehrmeyer, G.B.4
Ludolph, A.C.5
Kassubek, J.6
Tumani, H.7
-
60
-
-
1542300896
-
Cerebrospinal fluid Abeta42 levels in multiple system atrophy
-
Verbeek, M.M.; Abdo, W.F.; De Jong, D.; Horstink, M.W.; Kremer, B.P.; Bloem, B.R. Cerebrospinal fluid Abeta42 levels in multiple system atrophy. Mov. Disord., 2004, 19(2), 238-240
-
(2004)
Mov. Disord.
, vol.19
, Issue.2
, pp. 238-240
-
-
Verbeek, M.M.1
Abdo, W.F.2
De Jong, D.3
Horstink, M.W.4
Kremer, B.P.5
Bloem, B.R.6
-
61
-
-
0037295255
-
Cerebrospinal fluid Abeta42 is reduced in multiple system atrophy but normal in Parkinson's disease and progressive supranuclear palsy
-
DOI 10.1002/mds.10321
-
Holmberg, B.; Johnels, B.; Blennow, K.; Rosengren, L. Cerebrospinal fluid Abeta42 is reduced in multiple system atrophy but normal in Parkinson's disease and progressive supranuclear palsy. Mov. Disord., 2003, 18(2), 186-190 (Pubitemid 36305463)
-
(2003)
Movement Disorders
, vol.18
, Issue.2
, pp. 186-190
-
-
Holmberg, B.1
Johnels, B.2
Blennow, K.3
Rosengren, L.4
-
62
-
-
33750503078
-
CSF orexin levels of Parkinson's disease, dementia with Lewy bodies, progressive supranuclear palsy and corticobasal degeneration
-
DOI 10.1016/j.jns.2006.08.004, PII S0022510X06003686
-
Yasui, K.; Inoue, Y.; Kanbayashi, T.; Nomura, T.; Kusumi, M.; Nakashima, K. CSF orexin levels of Parkinson's disease, dementia with Lewy bodies, progressive supranuclear palsy and corticobasal degeneration. J. Neurol. Sci., 2006, 250(1-2), 120-123 (Pubitemid 44665944)
-
(2006)
Journal of the Neurological Sciences
, vol.250
, Issue.1-2
, pp. 120-123
-
-
Yasui, K.1
Inoue, Y.2
Kanbayashi, T.3
Nomura, T.4
Kusumi, M.5
Nakashima, K.6
-
63
-
-
60549100530
-
Levels of brain related proteins in cerebrospinal fluid: An aid in the differential diagnosis of parkinsonian disorders
-
Constantinescu, R.; Zetterberg, H.; Holmberg, B.; Rosengren, L. Levels of brain related proteins in cerebrospinal fluid: an aid in the differential diagnosis of parkinsonian disorders. Parkinsonism Relat. Disord., 2009, 15(3), 205-212
-
(2009)
Parkinsonism Relat. Disord.
, vol.15
, Issue.3
, pp. 205-212
-
-
Constantinescu, R.1
Zetterberg, H.2
Holmberg, B.3
Rosengren, L.4
-
64
-
-
58149229648
-
Tau forms in CSF as a reliable biomarker for progressive supranuclear palsy
-
Borroni, B.; Malinverno, M.; Gardoni, F.; Alberici, A.; Parnetti, L.; Premi, E.; Bonuccelli, U.; Grassi, M.; Perani, D.; Calabresi, P.; Di Luca, M.; Padovani, A. Tau forms in CSF as a reliable biomarker for progressive supranuclear palsy. Neurology, 2008, 71(22), 1796-1803
-
(2008)
Neurology
, vol.71
, Issue.22
, pp. 1796-1803
-
-
Borroni, B.1
Malinverno, M.2
Gardoni, F.3
Alberici, A.4
Parnetti, L.5
Premi, E.6
Bonuccelli, U.7
Grassi, M.8
Perani, D.9
Calabresi, P.10
Di Luca, M.11
Padovani, A.12
|