-
2
-
-
8944226575
-
Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): Report of the NINDS-SPSP International Workshop
-
Litvan I, Agid Y, Calne D, Campbell G, Dubois B, Duvoisin RC, Goetz CG, Golbe LI, Grafman J, Growdon JH, Hallett M, Jankovic J, Quinn NP, Tolosa E, Zee DS (1996) Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP International Workshop. Neurology 47, 1-9.
-
(1996)
Neurology
, vol.47
, pp. 1-9
-
-
Litvan, I.1
Agid, Y.2
Calne, D.3
Campbell, G.4
Dubois, B.5
Duvoisin, R.C.6
Goetz, C.G.7
Golbe, L.I.8
Grafman, J.9
Growdon, J.H.10
Hallett, M.11
Jankovic, J.12
Quinn, N.P.13
Tolosa, E.14
Zee, D.S.15
-
3
-
-
84925566619
-
Frontotemporal dementia and related disorders: Deciphering the enigma
-
Joseph KA (2008) Frontotemporal dementia and related disorders: deciphering the enigma. Ann Neurol 115, 39-53.
-
(2008)
Ann Neurol
, vol.115
, pp. 39-53
-
-
Joseph, K.A.1
-
4
-
-
0037595532
-
Frontotemporal degeneration, Pick's Disease, Pick Complex and Ravel
-
Kertesz A, Hillis A, Munoz D (2003) Frontotemporal degeneration, Pick's Disease, Pick Complex and Ravel. Ann Neurol 54 S5, S1-S2.
-
(2003)
Ann Neurol
, vol.54
, Issue.5
-
-
Kertesz, A.1
Hillis, A.2
Munoz, D.3
-
5
-
-
25144460507
-
A new mutation of the tau gene, G303V, in early-onset familial progressive supranuclear palsy
-
Ros R, Thobois S, Streichenberger N, Kopp N, Sanchez MP, Perez M, Hoenicka J, Avila J, Honnorat J, de Yebenes JG (2005) A new mutation of the tau gene, G303V, in early-onset familial progressive supranuclear palsy. Arch Neurol 62,1444-1450.
-
(2005)
Arch Neurol
, vol.62
, pp. 1444-1450
-
-
Ros, R.1
Thobois, S.2
Streichenberger, N.3
Kopp, N.4
Sanchez, M.P.5
Perez, M.6
Hoenicka, J.7
Avila, J.8
Honnorat, J.9
De Yebenes, J.G.10
-
6
-
-
33750576830
-
Novel splicing mutation in the progranulin gene causing familial corticobasal degeneration syndrome
-
Masellis M, Momeni P, Meschino W, Heffner R Jr, Elder J, Sato C, Liang Y, St George-Hyslop P, Hardy J, Bilbao J, Black S, Rogaeva E (2006) Novel splicing mutation in the progranulin gene causing familial corticobasal degeneration syndrome. Brain 129, 3115-3123.
-
(2006)
Brain
, vol.129
, pp. 3115-3123
-
-
Masellis, M.1
Momeni, P.2
Meschino, W.3
Heffner Jr., R.4
Elder, J.5
Sato, C.6
Liang, Y.7
St George-Hyslop, P.8
Hardy, J.9
Bilbao, J.10
Black, S.11
Rogaeva, E.12
-
7
-
-
68149108192
-
Familial aggregation of parkinsonism in progressive supra nuclear palsy
-
Donker Kaat L, Boon AJ, Azmani A, Kamphorst W, Breteler MM, Anar B, Heutink P, van Swieten JC (2009) Familial aggregation of parkinsonism in progressive supra nuclear palsy. Neurology 73, 98-105.
-
(2009)
Neurology
, vol.73
, pp. 98-105
-
-
Donker Kaat, L.1
Boon, A.J.2
Azmani, A.3
Kamphorst, W.4
Breteler, M.M.5
Anar, B.6
Heutink, P.7
Van Swieten, J.C.8
-
8
-
-
0033041179
-
Association of an extended haplotype in the tau gene with progressive supranuclear palsy
-
Baker M, Litvan I, Houlden H, Adamson J, Dickson D, Perez-Tur J, Hardy J, Lynch T, Bigio E, Hutton M (1999) Association of an extended haplotype in the tau gene with progressive supranuclear palsy. HumMol Genet 8, 711-715. (Pubitemid 29139987)
-
(1999)
Human Molecular Genetics
, vol.8
, Issue.4
, pp. 711-715
-
-
Baker, M.1
Litvan, I.2
Houlden, H.3
Adamson, J.4
Dickson, D.5
Perez-Tur, J.6
Hardy, J.7
Lynch, T.8
Bigio, E.9
Hutton, M.10
-
9
-
-
0035954364
-
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype
-
Houlden H, Baker M, Morris HR, MacDonald N, Pickering-Brown S, Adamson J, Lees AJ, Rossor MN, Quinn NP, Kertesz A, Khan MN, Hardy J, Lantos PL, St George-Hyslop P, Munoz DG, Mann D, Lang AE, Bergeron C, Bigio EH, Litvan I, Bha-tia KP, Dickson D, Wood NW, Hutton M (2001) Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype. Neurology 56, 1702-1706. (Pubitemid 32574570)
-
(2001)
Neurology
, vol.56
, Issue.12
, pp. 1702-1706
-
-
Houlden, H.1
Baker, M.2
Morris, H.R.3
MacDonald, N.4
Pickering-Brown, S.5
Adamson, J.6
Lees, A.J.7
Rossor, M.N.8
Quinn, N.P.9
Kertesz, A.10
Khan, M.N.11
Hardy, J.12
Lantos, P.L.13
George-Hyslop, P.14
Munoz, D.G.15
Mann, D.16
Lang, A.E.17
Bergeron, C.18
Bigio, E.H.19
Litvan, I.20
Bhatia, K.P.21
Dickson, D.22
Wood, N.W.23
Hutton, M.24
more..
-
10
-
-
55949134996
-
Role of the tau gene region chromosome inversion in progressive supranuclear palsy, corticobasal degeneration, and related disorders
-
Webb A, Miller B, Bonasera S, Boxer A, Karydas A, Wil-helmsen KC (2008) Role of the tau gene region chromosome inversion in progressive supranuclear palsy, corticobasal degeneration, and related disorders. Arch Neurol 65, 1473-1478.
-
(2008)
Arch Neurol
, vol.65
, pp. 1473-1478
-
-
Webb, A.1
Miller, B.2
Bonasera, S.3
Boxer, A.4
Karydas, A.5
Wil-Helmsen, K.C.6
-
11
-
-
33847178181
-
The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts
-
Myers AJ, Pittman AM, Zhao AS, Rohrer K, Kaleem M, Marlowe L, Lees A, Leung D, McKeith IG, Perry RH, Morris CM, Trojanowski JQ, Clark C, Karlawish J, Arnold S, Forman MS, Van Deerlin V, de Silva R, Hardy J (2007) The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts. Neurobiol Dis 25, 561-570.
-
(2007)
Neurobiol Dis
, vol.25
, pp. 561-570
-
-
Myers, A.J.1
Pittman, A.M.2
Zhao, A.S.3
Rohrer, K.4
Kaleem, M.5
Marlowe, L.6
Lees, A.7
Leung, D.8
McKeith, I.G.9
Perry, R.H.10
Morris, C.M.11
Trojanowski, J.Q.12
Clark, C.13
Karlawish, J.14
Arnold, S.15
Forman, M.S.16
Van Deerlin, V.17
De Silva, R.18
Hardy, J.19
-
12
-
-
33845361007
-
Haplotype-specific expression of exon 10 at the human MAPT locus
-
Caffrey TM, Joachim C, Paracchini S, Esiri MM, Wade-Martins R (2006) Haplotype-specific expression of exon 10 at the human MAPT locus. HumMol Genet 15, 3529-3537.
-
(2006)
HumMol Genet
, vol.15
, pp. 3529-3537
-
-
Caffrey, T.M.1
Joachim, C.2
Paracchini, S.3
Esiri, M.M.4
Wade-Martins, R.5
-
13
-
-
34147181052
-
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms
-
Melquist S, Craig DW, Huentelman MJ, Crook R, Pearson JV, Baker M, Zismann VL, Gass J, Adamson J, Szelinger S, Corn-eveaux J, Cannon A, Coon KD, Lincoln S, Adler C, Tuite P, Calne DB, Bigio EH, Uitti RJ, Wszolek ZK, Golbe LI, Caselli RJ, Graff-Radford N, Litvan I, Farrer MJ, Dickson DW, Hut-ton M, Stephan DA (2007) Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms. Am J Hum Genet 80, 769-778.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 769-778
-
-
Melquist, S.1
Craig, D.W.2
Huentelman, M.J.3
Crook, R.4
Pearson, J.V.5
Baker, M.6
Zismann, V.L.7
Gass, J.8
Adamson, J.9
Szelinger, S.10
Corn-Eveaux, J.11
Cannon, A.12
Coon, K.D.13
Lincoln, S.14
Adler, C.15
Tuite, P.16
Calne, D.B.17
Bigio, E.H.18
Uitti, R.J.19
Wszolek, Z.K.20
Golbe, L.I.21
Caselli, R.J.22
Graff-Radford, N.23
Litvan, I.24
Farrer, M.J.25
Dickson, D.W.26
Hut-Ton, M.27
Stephan, D.A.28
more..
-
14
-
-
50449108723
-
Preliminary evidence that VEGF genetic variability confers susceptibility to frontotemporal lobar degeneration
-
Borroni B, Ghezzi S, Agosti C, Archetti S, Fenoglio C, Galim-berti D, Scarpini E, Di Luca M, Bresolin N, Comi GP, Padovani A, Del Bo R (2008) Preliminary evidence that VEGF genetic variability confers susceptibility to frontotemporal lobar degeneration. Rejuvenation Res 11, 773-780.
-
(2008)
Rejuvenation Res
, vol.11
, pp. 773-780
-
-
Borroni, B.1
Ghezzi, S.2
Agosti, C.3
Archetti, S.4
Fenoglio, C.5
Galim-Berti, D.6
Scarpini, E.7
Di Luca, M.8
Bresolin, N.9
Comi, G.P.10
Padovani, A.11
Del Bo, R.12
-
15
-
-
2342667384
-
New roles for VEGF in nervous tissue-beyond blood vessels
-
Rosenstein JM, Krum JM (2004) New roles for VEGF in nervous tissue-beyond blood vessels. Exp Neurol 187, 246253.
-
(2004)
Exp Neurol
, vol.187
, pp. 246253
-
-
Rosenstein, J.M.1
Krum, J.M.2
-
16
-
-
16644382257
-
Treatment of motoneuron degeneration by intracerebroventricular delivery of VEGF in a rat model of ALS
-
Storkebaum E, Lambrechts D, Dewerchin M, Moreno-Murciano MP, Appelmans S, Oh H, Van Damme P, Rutten B, Man WY, De Mol M, Wyns S, Manka D, Vermeulen K, Van Den Bosch L, Mertens N, Schmitz C, Robberecht W, Conway EM, Collen D, Moons L, Carmeliet P (2005) Treatment of motoneuron degeneration by intracerebroventricular delivery of VEGF in a rat model of ALS. Nat Neurosci 8, 85-92.
-
(2005)
Nat Neurosci
, vol.8
, pp. 85-92
-
-
Storkebaum, E.1
Lambrechts, D.2
Dewerchin, M.3
Moreno-Murciano, M.P.4
Appelmans, S.5
Oh, H.6
Van Damme, P.7
Rutten, B.8
Man, W.Y.9
De Mol, M.10
Wyns, S.11
Manka, D.12
Vermeulen, K.13
Van Den Bosch, L.14
Mertens, N.15
Schmitz, C.16
Robberecht, W.17
Conway, E.M.18
Collen, D.19
Moons, L.20
Carmeliet, P.21
more..
-
17
-
-
0034764622
-
Clinical and pathological diagnosis of frontotemporal dementia: Report of the Work Group on Frontotemporal Dementia and Pick's Disease
-
Work Group on Frontotemporal Dementia and Pick's Disease
-
McKhann GM, Albert MS, Grossman M, Miller B, Dickson D, Trojanowski JQ; Work Group on Frontotemporal Dementia and Pick's Disease (2001) Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease. Arch Neurol 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
-
18
-
-
0028361508
-
Noise properties of the em algorithm: I theory
-
Barrett HH, Wilson DW, Tsui BM (1994) Noise properties of the EM algorithm: I. Theory. Phys Med Biol 39, 833-846.
-
(1994)
Phys Med Biol
, vol.39
, pp. 833-846
-
-
Barrett, H.H.1
Wilson, D.W.2
Tsui, B.M.3
-
19
-
-
34249052182
-
Genetic variation at the tau locus and clinical syndromes associated with progressive supranuclear palsy
-
Williams DR, Pittman AM, Revesz T, Lees AJ, de Silva R (2007) Genetic variation at the tau locus and clinical syndromes associated with progressive supranuclear palsy. Mov Disord 22, 895-897.
-
(2007)
Mov Disord
, vol.22
, pp. 895-897
-
-
Williams, D.R.1
Pittman, A.M.2
Revesz, T.3
Lees, A.J.4
De Silva, R.5
-
20
-
-
3843131833
-
Novel haplotypes in 17q21 are associated with progressive supranuclear palsy
-
Pastor P, Ezquerra M, Perez JC, Chakraverty S, Norton J, Racette BA, McKeel D, Perlmutter JS, Tolosa E, Goate AM. Novel haplotypes in 17q21 are associated with progressive supranuclear palsy. Ann Neurol 56, 249-528.
-
Ann Neurol
, vol.56
, pp. 249-528
-
-
Pastor, P.1
Ezquerra, M.2
Perez, J.C.3
Chakraverty, S.4
Norton, J.5
Racette, B.A.6
McKeel, D.7
Perlmutter, J.S.8
Tolosa, E.9
Goate, A.M.10
-
21
-
-
0036445830
-
Vascular and neuronal effects of VEGF in the nervous system: Implications for neurological disorders
-
Carmeliet P, Storkebaum E (2002) Vascular and neuronal effects of VEGF in the nervous system: implications for neurological disorders. Semin CellDevBiol 13, 39-53.
-
(2002)
Semin CellDevBiol
, vol.13
, pp. 39-53
-
-
Carmeliet, P.1
Storkebaum, E.2
-
22
-
-
67649973540
-
Role and therapeutic potentials of VEGF in the nervous system
-
De Almodovar CR, Lambrechts D, Mazzone M, Carmeliet P (2009) Role and therapeutic potentials of VEGF in the nervous system. Physion Rev 89, 607-648.
-
(2009)
Physion Rev
, vol.89
, pp. 607-648
-
-
De Almodovar, C.R.1
Lambrechts, D.2
Mazzone, M.3
Carmeliet, P.4
-
23
-
-
0037442985
-
Haplotype analysis of the polymorphic human vascular en-dothelial growth factor gene promoter
-
Stevens A, Soden J, Brenchley PE, Ralph S, Ray DW (2003) Haplotype analysis of the polymorphic human vascular en-dothelial growth factor gene promoter. Cancer Res 63, 812-816.
-
(2003)
Cancer Res
, vol.63
, pp. 812-816
-
-
Stevens, A.1
Soden, J.2
Brenchley, P.E.3
Ralph, S.4
Ray, D.W.5
-
24
-
-
20044378293
-
Vascular endothelial growth factor gene variability is associated with increased risk for AD
-
Del Bo R, Scarlato M, Ghezzi S, Martinelli Boneschi F, Fenoglio C, Galbiati S, Virgilio R, Galimberti D, Galimberti G, Crimi M, Ferrarese C, Scarpini E, Bresolin N, Comi GP, Del Bo R, Scarlato M, Ghezzi S, Martinelli Boneschi F, Fenoglio C, Galbiati S, Virgilio R, Galimberti D, Galimberti G, Crimi M, Ferrarese C, Scarpini E, Bresolin N, Comi GPF. Vascular endothelial growth factor gene variability is associated with increased risk for AD. Ann Neurol 57, 373-380.
-
Ann Neurol
, vol.57
, pp. 373-380
-
-
Del Bo, R.1
Scarlato, M.2
Ghezzi, S.3
Martinelli Boneschi, F.4
Fenoglio, C.5
Galbiati, S.6
Virgilio, R.7
Galimberti, D.8
Galimberti, G.9
Crimi, M.10
Ferrarese, C.11
Scarpini, E.12
Bresolin, N.13
Comi, G.P.14
Del Bo, R.15
Scarlato, M.16
Ghezzi, S.17
Martinelli Boneschi, F.18
Fenoglio, C.19
Galbiati, S.20
Virgilio, R.21
Galimberti, D.22
Galimberti, G.23
Crimi, M.24
Ferrarese, C.25
Scarpini, E.26
Bresolin, N.27
Gpf, C.28
more..
-
25
-
-
33846228854
-
VEGF gene and phenotype relation with Alzheimer's disease and mild cognitive impairment
-
Chiappelli M, Borroni B, Archetti S, Calabrese E, Corsi MM, Franceschi M, Padovani A, Licastro F (2006) VEGF gene and phenotype relation with Alzheimer's disease and mild cognitive impairment. Rejuvenation Res 9, 485-493.
-
(2006)
Rejuvenation Res
, vol.9
, pp. 485-493
-
-
Chiappelli, M.1
Borroni, B.2
Archetti, S.3
Calabrese, E.4
Corsi, M.M.5
Franceschi, M.6
Padovani, A.7
Licastro, F.8
-
26
-
-
0041903805
-
VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death
-
Lambrechts D, Storkebaum E, Morimoto M, Del-Favero J, Desmet F, Marklund SL, Wyns S, Thijs V, Andersson J, van Marion I, Al-Chalabi A, Bornes S, Musson R, Hansen V, Beck-man L, Adolfsson R, Pall HS, Prats H, Vermeire S, Rutgeerts P, Katayama S, Awata T, Leigh N, Lang-Lazdunski L, Dewerchin M, Shaw C, Moons L, Vlietinck R, Morrison KE, Robberecht W, Van Broeckhoven C, Collen D, Andersen PM, Carmeliet P (2003) VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death. Nat Genet 34, 383-389.
-
(2003)
Nat Genet
, vol.34
, pp. 383-389
-
-
Lambrechts, D.1
Storkebaum, E.2
Morimoto, M.3
Del-Favero, J.4
Desmet, F.5
Marklund, S.L.6
Wyns, S.7
Thijs, V.8
Andersson, J.9
Van Marion, I.10
Al-Chalabi, A.11
Bornes, S.12
Musson, R.13
Hansen, V.14
Beck-Man, L.15
Adolfsson, R.16
Pall, H.S.17
Prats, H.18
Vermeire, S.19
Rutgeerts, P.20
Katayama, S.21
Awata, T.22
Leigh, N.23
Lang-Lazdunski, L.24
Dewerchin, M.25
Shaw, C.26
Moons, L.27
Vlietinck, R.28
Morrison, K.E.29
Robberecht, W.30
Van Broeckhoven, C.31
Collen, D.32
Andersen, P.M.33
Carmeliet, P.34
more..
|