-
2
-
-
1942440928
-
Non-Alzheimer's Disease Dementias: Anatomic, Clinical, and Molecular Correlates
-
Hou CE, Carlin D, Miller BL. Non-Alzheimer's disease dementias: anatomic, clinical, and molecular correlates. Can J Psychiatry 2004 49 : 164 171. (Pubitemid 38506494)
-
(2004)
Canadian Journal of Psychiatry
, vol.49
, Issue.3
, pp. 164-171
-
-
Hou, C.E.1
Carlin, D.2
Miller, B.L.3
-
3
-
-
0031672540
-
Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria
-
Neary D, Snowden JS, Gustafson L, et al. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology 1998 51 : 1546 1554.
-
(1998)
Neurology
, vol.51
, pp. 1546-1554
-
-
Neary, D.1
Snowden, J.S.2
Gustafson, L.3
-
4
-
-
29144489408
-
Progressive, isolated language disturbance: Its significance in a 65-year-old-man. A case report with implications for treatment and review of literature
-
DOI 10.1016/j.jns.2005.09.006, PII S0022510X05003333
-
Scarpini E, Galimberti D, Guidi I, Bresolin N, Scheltens P. Progressive, isolated language disturbance: its significance in a 65-year-old-man. A case report with implications for treatment and review of literature. J Neurol Sci 2006 240 : 45 51. (Pubitemid 41814952)
-
(2006)
Journal of the Neurological Sciences
, vol.240
, Issue.1-2
, pp. 45-51
-
-
Scarpini, E.1
Galimberti, D.2
Guidi, I.3
Bresolin, N.4
Scheltens, P.5
-
5
-
-
33749568019
-
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
-
DOI 10.1093/hmg/ddl241
-
Gass J, Cannon A, Mackenzie IR, et al. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. Hum Mol Genet 2006 15 : 2988 3001. (Pubitemid 44530703)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.20
, pp. 2988-3001
-
-
Gass, J.1
Cannon, A.2
Mackenzie, I.R.3
Boeve, B.4
Baker, M.5
Adamson, J.6
Crook, R.7
Melquist, S.8
Kuntz, K.9
Petersen, R.10
Josephs, K.11
Pickering-Brown, S.M.12
Graff-Radford, N.13
Uitti, R.14
Dickson, D.15
Wszolek, Z.16
Gonzalez, J.17
Beach, T.G.18
Bigio, E.19
Johnson, N.20
Weintraub, S.21
Mesulam, M.22
White III, C.L.23
Woodruff, B.24
Caselli, R.25
Hsiung, G.-Y.26
Feldman, H.27
Knopman, D.28
Hutton, M.29
Rademakers, R.30
more..
-
6
-
-
5044235577
-
The role of tau (MAPT) in frontotemporal dementia and related tauopathies
-
DOI 10.1002/humu.20086
-
Rademakers R, Cruts M, van Broekhoven C. The role of tau (MAPT) in frontotemporal dementia and related tauopathies. Hum Mutat 2004 24 : 277 295. (Pubitemid 39336634)
-
(2004)
Human Mutation
, vol.24
, Issue.4
, pp. 277-295
-
-
Rademakers, R.1
Cruts, M.2
Van Broeckhoven, C.3
-
7
-
-
42249085980
-
Refining frontotemporal dementia with parkinsonism linked to chromosome 17
-
Boeve BF, Hutton M. Refining frontotemporal dementia with parkinsonism linked to chromosome 17. Arch Neurol 2008 65 : 460 464.
-
(2008)
Arch Neurol
, vol.65
, pp. 460-464
-
-
Boeve, B.F.1
Hutton, M.2
-
8
-
-
21744455599
-
The conserved protein DCN-1/Dcn1p is required for cullin neddylation in C. elegans and S. cerevisiae
-
DOI 10.1038/nature03662
-
Kurz T, Özlü N, Rudolf F, et al. The conserved protein DCN-1/Dcn1p is required for cullin neddylation in C. elegans and S. cerevisiae. Nature 2005 435 : 1257 1261. (Pubitemid 40943092)
-
(2005)
Nature
, vol.435
, Issue.7046
, pp. 1257-1261
-
-
Kurz, T.1
Ozlu, N.2
Rudolf, F.3
O'Rourke, S.M.4
Luke, B.5
Hofmann, K.6
Hyman, A.A.7
Bowerman, B.8
Peter, M.9
-
9
-
-
0033070197
-
High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands
-
Rizzu P, Van Swieten JC, Joosse M, et al. High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands. Am J Hum Genet 1999 64 : 414 421. (Pubitemid 129500524)
-
(1999)
American Journal of Human Genetics
, vol.64
, Issue.2
, pp. 414-421
-
-
Rizzu, P.1
Van Swieten, J.C.2
Joosse, M.3
Hasegawa, M.4
Stevens, M.5
Tibben, A.6
Niermeijer, M.F.7
Hillebrand, M.8
Ravid, R.9
Oostra, B.A.10
Goedert, M.11
Van Duijn, C.M.12
Heutink, P.13
-
10
-
-
38949174973
-
A novel deletion in progranulin gene is associated with FTDP-17 and CBS
-
Benussi L, Binetti G, Sina E, et al. A novel deletion in progranulin gene is associated with FTDP-17 and CBS. Neurobiol Aging 2008 29 : 427 435.
-
(2008)
Neurobiol Aging
, vol.29
, pp. 427-435
-
-
Benussi, L.1
Binetti, G.2
Sina, E.3
-
11
-
-
51349151222
-
Novel exon 1 progranulin gene variant in Alzheimer's disease
-
Cortini F, Fenoglio C, Guidi I, et al. Novel exon 1 progranulin gene variant in Alzheimer's disease. Eur J Neurol 2008 15 : 1111 1117.
-
(2008)
Eur J Neurol
, vol.15
, pp. 1111-1117
-
-
Cortini, F.1
Fenoglio, C.2
Guidi, I.3
-
12
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
DOI 10.1126/science.1069424
-
Gabriel SB, Schaffner SF, Nguyen H, et al. The structure of haplotype blocks in the human genome. Science 2002 296 : 2225 2229. (Pubitemid 34680308)
-
(2002)
Science
, vol.296
, Issue.5576
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
Higgins, J.7
DeFelice, M.8
Lochner, A.9
Faggart, M.10
Liu-Cordero, S.N.11
Rotimi, C.12
Adeyemo, A.13
Cooper, R.14
Ward, R.15
Lander, E.S.16
Daly, M.J.17
Altshuler, D.18
-
13
-
-
46149083470
-
Progranulin genetic variations in frontotemporal lobar degeneration: Evidence for low mutation frequency in Italian clinical series
-
Borroni B, Archetti S, Alberici A, et al. Progranulin genetic variations in frontotemporal lobar degeneration: evidence for low mutation frequency in Italian clinical series. Neurogenetics 2008 9 : 197 205.
-
(2008)
Neurogenetics
, vol.9
, pp. 197-205
-
-
Borroni, B.1
Archetti, S.2
Alberici, A.3
-
14
-
-
0032850581
-
Clinical and pathological evidence for a frontal variant of Alzheimer disease
-
DOI 10.1001/archneur.56.10.1233
-
Johnson JK, Head E, Kim R, Starr A, Cotman CW. Clinical and pathological evidence for a frontal variant of Alzheimer disease. Arch Neurol 1999 56 : 1233 1239. (Pubitemid 29473215)
-
(1999)
Archives of Neurology
, vol.56
, Issue.10
, pp. 1233-1239
-
-
Johnson, J.K.1
Head, E.2
Kim, R.3
Starr, A.4
Cotman, C.W.5
|