-
1
-
-
33847212830
-
Frontotemporal lobar degeneration: Current concepts in the light of recent advances
-
Kumar-Singh S, Van Broeckhoven C. Frontotemporal lobar degeneration: current concepts in the light of recent advances. Brain Pathol 2007;17:104-14.
-
(2007)
Brain Pathol
, vol.17
, pp. 104-114
-
-
Kumar-Singh, S.1
Van Broeckhoven, C.2
-
2
-
-
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;51:1546-54.
-
(1998)
Neurology
, vol.51
, pp. 1546-1554
-
-
Neary, D.1
Snowden, J.S.2
Gustafson, L.3
-
3
-
-
84866490231
-
The molecular basis of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum
-
Van Langenhove T, Van der Zee J, Van Broeckhoven C, et al. The molecular basis of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum. Ann Med 2012;44:817-28.
-
(2012)
Ann Med
, vol.44
, pp. 817-828
-
-
Van Langenhove, T.1
Van Der Zee, J.2
Van Broeckhoven, C.3
-
4
-
-
77649187519
-
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: An update
-
Mackenzie IR, Neumann M, Bigio EH, et al. Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update. Acta Neuropathol 2010;119:1-4.
-
(2010)
Acta Neuropathol
, vol.119
, pp. 1-4
-
-
Mackenzie, I.R.1
Neumann, M.2
Bigio, E.H.3
-
5
-
-
0031800415
-
Familial aggregation in frontotemporal dementia
-
Stevens M, Van Duijn CM, Kamphorst W, et al. Familial aggregation in frontotemporal dementia. Neurology 1998;50:1541-5. (Pubitemid 28283216)
-
(1998)
Neurology
, vol.50
, Issue.6
, 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
-
6
-
-
33746919083
-
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
-
DOI 10.1038/nature05016, PII NATURE05016
-
Baker M, Mackenzie IR, Pickering-Brown SM, et al. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 2006;442:916-9. (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..
-
7
-
-
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, et al. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 2006;442:920-4. (Pubitemid 44285947)
-
(2006)
Nature
, vol.442
, Issue.7105
, pp. 920-924
-
-
Cruts, M.1
Gijselinck, I.2
Van Der, Z.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, B.M.17
Cuijt, I.18
Vennekens, K.19
De Deyn, P.P.20
Kumar-Singh, S.21
Van Broeckhoven, C.22
more..
-
8
-
-
7344220963
-
Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism
-
DOI 10.1093/hmg/7.11.1825
-
Dumanchin C, Camuzat A, Campion D, et al. Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism. Hum Mol Genet 1998;7:1825-9. (Pubitemid 28464159)
-
(1998)
Human Molecular Genetics
, vol.7
, Issue.11
, pp. 1825-1829
-
-
Dumanchin, C.1
Camuzat, A.2
Campion, D.3
Verpillat, P.4
Hannequin, D.5
Dubois, B.6
Saugier-Veber, P.7
Martin, C.8
Penet, C.9
Charbonnier, F.10
Agid, Y.11
Frebourg, T.12
Brice, A.13
-
9
-
-
80054832080
-
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
-
DeJesus-Hernandez M, Mackenzie IR, Boeve BF, et al. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 2011;72:245-56.
-
(2011)
Neuron
, vol.72
, pp. 245-256
-
-
DeJesus-Hernandez, M.1
Mackenzie, I.R.2
Boeve, B.F.3
-
10
-
-
83555166183
-
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: A gene identification study
-
Gijselinck I, Van Langenhove T, Van der Zee J, et al. A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study. Lancet Neurol 2012;11:54-65.
-
(2012)
Lancet Neurol
, vol.11
, pp. 54-65
-
-
Gijselinck, I.1
Van Langenhove, T.2
Van Der Zee, J.3
-
11
-
-
80054837386
-
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
-
Renton AE, Majounie E, Waite A, et al. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 2011;72:257-68.
-
(2011)
Neuron
, vol.72
, pp. 257-268
-
-
Renton, A.E.1
Majounie, E.2
Waite, A.3
-
12
-
-
84873093810
-
A pan-European study of the C9orf72 repeat associated with FTLD: Geographic prevalence, genomic instability, and intermediate repeats
-
Van der Zee J, Gijselinck I, Dillen L, et al. A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats. Hum Mutat 2013;34:363-73.
-
(2013)
Hum Mutat
, vol.34
, pp. 363-373
-
-
Van Der Zee, J.1
Gijselinck, I.2
Dillen, L.3
-
13
-
-
33750716074
-
TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
DOI 10.1016/j.bbrc.2006.10.093, PII S0006291X06023187
-
Arai T, Hasegawa M, Akiyama H, et al. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem Biophys Res Commun 2006;351:602-11. (Pubitemid 44708852)
-
(2006)
Biochemical and Biophysical Research Communications
, vol.351
, Issue.3
, pp. 602-611
-
-
Arai, T.1
Hasegawa, M.2
Akiyama, H.3
Ikeda, K.4
Nonaka, T.5
Mori, H.6
Mann, D.7
Tsuchiya, K.8
Yoshida, M.9
Hashizume, Y.10
Oda, T.11
-
14
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
DOI 10.1126/science.1134108
-
Neumann M, Sampathu DM, Kwong LK, et al. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 2006;314:130-3. (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
-
15
-
-
65649112431
-
TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration
-
Benajiba L, Le Ber I, Camuzat A, et al. TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration. Ann Neurol 2009;65:470-3.
-
(2009)
Ann Neurol
, vol.65
, pp. 470-473
-
-
Benajiba, L.1
Le Ber, I.2
Camuzat, A.3
-
16
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
DOI 10.1126/science.1154584
-
Sreedharan J, Blair IP, Tripathi VB, et al. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 2008;319:1668-72. (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
-
17
-
-
82755161705
-
Biomarkers in frontotemporal lobar degenerations-progress and challenges
-
Hu WT, Trojanowski JQ, Shaw LM. Biomarkers in frontotemporal lobar degenerations-progress and challenges. Prog Neurobiol 2011;95:636-48.
-
(2011)
Prog Neurobiol
, vol.95
, pp. 636-648
-
-
Hu, W.T.1
Trojanowski, J.Q.2
Shaw, L.M.3
-
18
-
-
47949108734
-
TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer's disease and frontotemporal lobar degeneration
-
Foulds P, McAuley E, Gibbons L, et al. TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer's disease and frontotemporal lobar degeneration. Acta Neuropathol 2008;116:141-6.
-
(2008)
Acta Neuropathol
, vol.116
, pp. 141-146
-
-
Foulds, P.1
McAuley, E.2
Gibbons, L.3
-
19
-
-
70449526407
-
Plasma phosphorylated-TDP-43 protein levels correlate with brain pathology in frontotemporal lobar degeneration
-
Foulds PG, Davidson Y, Mishra M, et al. Plasma phosphorylated-TDP-43 protein levels correlate with brain pathology in frontotemporal lobar degeneration. Acta Neuropathol 2009;118:647-58.
-
(2009)
Acta Neuropathol
, vol.118
, pp. 647-658
-
-
Foulds, P.G.1
Davidson, Y.2
Mishra, M.3
-
20
-
-
57049149602
-
Increased TDP-43 protein in cerebrospinal fluid of patients with amyotrophic lateral sclerosis
-
Kasai T, Tokuda T, Ishigami N, et al. Increased TDP-43 protein in cerebrospinal fluid of patients with amyotrophic lateral sclerosis. Acta Neuropathol 2009;117:55-62.
-
(2009)
Acta Neuropathol
, vol.117
, pp. 55-62
-
-
Kasai, T.1
Tokuda, T.2
Ishigami, N.3
-
21
-
-
55949089475
-
TDP-43 in cerebrospinal fluid of patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Steinacker P, Hendrich C, Sperfeld AD, et al. TDP-43 in cerebrospinal fluid of patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Arch Neurol 2008;65:1481-7.
-
(2008)
Arch Neurol
, vol.65
, pp. 1481-1487
-
-
Steinacker, P.1
Hendrich, C.2
Sperfeld, A.D.3
-
22
-
-
79952739268
-
PICOGEN: Five years experience with a genetic counselling program for dementia
-
Fortea J, Lladó A, Clarimón J, et al. PICOGEN: five years experience with a genetic counselling program for dementia. Neurologia 2011;26:143-9.
-
(2011)
Neurologia
, vol.26
, pp. 143-149
-
-
Fortea, J.1
Lladó, A.2
Clarimón, J.3
-
23
-
-
80052938441
-
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
-
Rascovsky K, Hodges JR, Knopman D, et al. Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain 2011;134:2456-77.
-
(2011)
Brain
, vol.134
, pp. 2456-2477
-
-
Rascovsky, K.1
Hodges, J.R.2
Knopman, D.3
-
24
-
-
79952823979
-
Classification of primary progressive aphasia and its variants
-
Gorno-Tempini ML, Hillis A, Weintraub S, et al. Classification of primary progressive aphasia and its variants. Neurology 2011;76:1006-14.
-
(2011)
Neurology
, vol.76
, pp. 1006-1014
-
-
Gorno-Tempini, M.L.1
Hillis, A.2
Weintraub, S.3
-
25
-
-
84865592580
-
Serum progranulin levels in patients with frontotemporal lobar degeneration and Alzheimer's disease: Detection of GRN mutations in a Spanish cohort
-
Antonell A, Gil S, Sánchez-Valle R, et al . Serum progranulin levels in patients with frontotemporal lobar degeneration and Alzheimer's disease: detection of GRN mutations in a Spanish cohort. J Alzheimers Dis 2012;31:581-91.
-
(2012)
J Alzheimers Dis
, vol.31
, pp. 581-591
-
-
Antonell, A.1
Gil, S.2
Sánchez-Valle, R.3
-
26
-
-
84861919479
-
Expansion mutation in C9ORF72 does not influence plasma progranulin levels in frontotemporal dementia
-
Dols-Icardo O, Suárez-Calvet M, Hernández I, et al. Expansion mutation in C9ORF72 does not influence plasma progranulin levels in frontotemporal dementia. Neurobiol Aging 2012;33:1851.e17-19.
-
(2012)
Neurobiol Aging
, vol.33
-
-
Dols-Icardo, O.1
Suárez-Calvet, M.2
Hernández, I.3
-
27
-
-
84881421614
-
Comparison of 2 diagnostic criteria for the behavioral variant of frontotemporal dementia
-
Costa S, Suárez-Calvet M, Antón S, et al. Comparison of 2 diagnostic criteria for the behavioral variant of frontotemporal dementia. Am J Alzheimers Dis Other Demen 2013;28:469-76.
-
(2013)
Am J Alzheimers Dis Other Demen
, vol.28
, pp. 469-476
-
-
Costa, S.1
Suárez-Calvet, M.2
Antón, S.3
-
28
-
-
67651204382
-
CSF biomarkers and incipient Alzheimer disease in patients with mild cognitive impairment
-
Mattsson N, Zetterberg H, Hansson O, et al. CSF biomarkers and incipient Alzheimer disease in patients with mild cognitive impairment. JAMA 2009;302:385-93.
-
(2009)
JAMA
, vol.302
, pp. 385-393
-
-
Mattsson, N.1
Zetterberg, H.2
Hansson, O.3
-
29
-
-
1542349913
-
Beta-Secretase Activity Increases with Aging in Human, Monkey, and Mouse Brain
-
Fukumoto H, Rosene DL, Moss MB, et al. Beta-secretase activity increases with aging in human, monkey, and mouse brain. Am J Pathol 2004;164:719-25. (Pubitemid 38364685)
-
(2004)
American Journal of Pathology
, vol.164
, Issue.2
, pp. 719-725
-
-
Fukumoto, H.1
Rosene, D.L.2
Moss, M.B.3
Raju, S.4
Hyman, B.T.5
Irizarry, M.C.6
-
30
-
-
84892451456
-
Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia
-
Published Online First: 20 September doi:10.1093/hmg/ddt460
-
Dols-Icardo O, García-Redondo A, Rojas-García R, et al. Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia. Hum Mol Genet Published Online First: 20 September 2013. doi:10.1093/hmg/ddt460
-
(2013)
Hum Mol Genet
-
-
Dols-Icardo, O.1
García-Redondo, A.2
Rojas-García, R.3
-
31
-
-
79960835044
-
Neuropathological background of phenotypical variability in frontotemporal dementia
-
Josephs KA, Hodges JR, Snowden JS, et al. Neuropathological background of phenotypical variability in frontotemporal dementia. Acta Neuropathol 2011;122:137-53.
-
(2011)
Acta Neuropathol
, vol.122
, pp. 137-153
-
-
Josephs, K.A.1
Hodges, J.R.2
Snowden, J.S.3
-
32
-
-
64849103956
-
Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members
-
Finch N, Baker M, Crook R, et al. Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members. Brain 2009;132:583-91.
-
(2009)
Brain
, vol.132
, pp. 583-591
-
-
Finch, N.1
Baker, M.2
Crook, R.3
-
33
-
-
54449085260
-
Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration
-
Ghidoni R, Benussi L, Glionna M, et al. Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration. Neurology 2008;71:1235-9.
-
(2008)
Neurology
, vol.71
, pp. 1235-1239
-
-
Ghidoni, R.1
Benussi, L.2
Glionna, M.3
-
34
-
-
67249111266
-
Serum biomarker for progranulin-associated frontotemporal lobar degeneration
-
Sleegers K, Brouwers N, Van Damme P, et al. Serum biomarker for progranulin-associated frontotemporal lobar degeneration. Ann Neurol 2009;65:603-9.
-
(2009)
Ann Neurol
, vol.65
, pp. 603-609
-
-
Sleegers, K.1
Brouwers, N.2
Van Damme, P.3
-
35
-
-
77949423619
-
Cerebrospinal fluid and plasma biomarkers in Alzheimer disease
-
Blennow K, Hampel H, Weiner M, et al. Cerebrospinal fluid and plasma biomarkers in Alzheimer disease. Nat Rev Neurol 2010;6:131-44.
-
(2010)
Nat Rev Neurol
, vol.6
, pp. 131-144
-
-
Blennow, K.1
Hampel, H.2
Weiner, M.3
-
36
-
-
43249106998
-
CSF biomarkers in frontotemporal lobar degeneration with known pathology
-
DOI 10.1212/01.wnl.0000311445.21321.fc, PII 0000611420080506100015
-
Bian H, Van Swieten JC, Leight S, et al. CSF biomarkers in frontotemporal lobar degeneration with known pathology. Neurology 2008;70:1827-35. (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
-
37
-
-
84863423724
-
Cerebrospinal fluid amyloid-β 2-42 is decreased in Alzheimer's, but not in frontotemporal dementia
-
Bibl M, Gallus M, Welge V, et al. Cerebrospinal fluid amyloid-β 2-42 is decreased in Alzheimer's, but not in frontotemporal dementia. J Neural Transm 2012;119:805-13.
-
(2012)
J Neural Transm
, vol.119
, pp. 805-813
-
-
Bibl, M.1
Gallus, M.2
Welge, V.3
-
38
-
-
43249091150
-
Diagnostic value of CSF biomarker profile in frontotemporal lobar degeneration
-
DOI 10.1097/WAD.0b013e3181610fea, PII 0000209320080100000007
-
Kapaki E, Paraskevas GP, Papageorgiou SG, et al. Diagnostic value of CSF biomarker profile in frontotemporal lobar degeneration. Alzheimer Dis Assoc Disord 2008;22:47-53. (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
-
39
-
-
77957317483
-
The multiple roles of TDP-43 in pre-mRNA processing and gene expression regulation
-
Buratti E, Baralle FE. The multiple roles of TDP-43 in pre-mRNA processing and gene expression regulation. RNA Biol 2010;7:420-9.
-
(2010)
RNA Biol
, vol.7
, pp. 420-429
-
-
Buratti, E.1
Baralle, F.E.2
-
40
-
-
59249085091
-
Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies
-
Neumann M, Kwong LK, Lee EB, et al. Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies. Acta Neuropathol 2009;117:137-49.
-
(2009)
Acta Neuropathol
, vol.117
, pp. 137-149
-
-
Neumann, M.1
Kwong, L.K.2
Lee, E.B.3
|