-
1
-
-
0031672540
-
Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria
-
Neary D, Snowden JS, Gustafson L, Passant U, Stuss D, Black S, Freedman M, Kertesz A, Robert PH, Albert M, Boone K, Miller BL, Cummings J, Benson DF (1998) Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria. Neurology 51, 1546-1554.
-
(1998)
Neurology
, vol.51
, 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
-
2
-
-
0041320789
-
Frontotemporal dementia in The Netherlands: Patient characteristics and prevalence estimates from a population-based study
-
DOI 10.1093/brain/awg204
-
Rosso SM, Donker Kaat L, Baks T, Joosse M, de Koning I, Pijnenburg Y, de Jong D, Dooijes D, Kamphorst W, Ravid R, Niermeijer MF, Verheij F, Kremer HP, Scheltens P, van Duijn CM, Heutink P, van Swieten JC (2003) Frontotemporal dementia in The Netherlands: Patient characteristics and prevalence estimates from a population-based study. Brain 126, 2016-2022. (Pubitemid 37059441)
-
(2003)
Brain
, vol.126
, Issue.9
, pp. 2016-2022
-
-
Rosso, S.M.1
Kaat, L.D.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
-
3
-
-
0032543684
-
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
-
Hutton M, Lendon CL, 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 RC, Stevens M, de Graaff E, Wauters E, van Baren J, Hillebrand M, Joosse M, Kwon JM, Nowotny P, Che LK, Norton J, Morris JC, Reed LA, Trojanowski J, Basun H, Lannfelt L, Neystat M, Fahn S, Dark F, Tannenberg T, Dodd PR, Hayward N, Kwok JB, Schofield PR, Andreadis A, Snowden J, Craufurd D, Neary D, Owen F, Oostra BA, Hardy J, Goate A, van Swieten J, Mann D, Lynch T, Heutink P (1998) Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 393, 702-705.
-
(1998)
Nature
, vol.393
, pp. 702-705
-
-
Hutton, M.1
Lendon, C.L.2
Rizzu, P.3
Baker, M.4
Froelich, S.5
Houlden, 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
Stevens, 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.38
Schofield, P.R.39
Andreadis, A.40
Snowden, J.41
Craufurd, D.42
Neary, D.43
Owen, F.44
Oostra, B.A.45
Hardy, J.46
Goate, A.47
Van Swieten, J.48
Mann, D.49
Lynch, T.50
Heutink, P.51
more..
-
4
-
-
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, Gass J, Rademakers R, Lindholm C, Snowden J, Adamson J, Sadovnick AD, Rollinson S, Cannon A, Dwosh E, Neary D, Melquist S, Richardson A, Dickson D, Berger Z, Eriksen J, Robinson T, Zehr C, Dickey CA, Crook R, McGowan E, Mann D, Boeve B, Feldman H, HuttonM (2006) Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 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..
-
5
-
-
33846055457
-
Progranulin mutations in ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
-
DOI 10.2174/156720506779025251
-
Cruts M, Kumar-Singh S, Van Broeckhoven C (2006) Progranulin mutations in ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Curr Alzheimer Res 3, 485-491. (Pubitemid 46066424)
-
(2006)
Current Alzheimer Research
, vol.3
, Issue.5
, pp. 485-491
-
-
Cruts, M.1
Kumar-Singh, S.2
Van Broeckhoven, C.3
-
6
-
-
80054837386
-
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
-
Renton AE, Majounie E, Waite A, Simon-Sanchez J, Rollinson S, Gibbs JR, Schymick JC, Laaksovirta H, van Swieten JC, Myllykangas L, Kalimo H, Paetau A, Abramzon Y, Remes AM, Kaganovich A, Scholz SW, Duckworth J, Ding J, Harmer DW, Hernandez DG, Johnson JO, Mok K, Ryten M, Trabzuni D, Guerreiro RJ, Orrell RW, Neal J, Murray A, Pearson J, Jansen IE, Sondervan D, Seelaar H, Blake D, Young K, Halliwell N, Callister JB, Toulson G, Richardson A, Gerhard A, Snowden J, Mann D, Neary D, Nalls MA, Peuralinna T, Jansson L, Isoviita VM, Kaivorinne AL, Holtta-Vuori M, Ikonen E, Sulkava R, Benatar M, Wuu J, Chio A, Restagno G, Borghero G, Sabatelli M, The ITALSGEN, Consortium, Heckerman D, Rogaeva E, Zinman L, Rothstein JD, Sendtner M, Drepper C, Eichler EE, Alkan C, Abdullaev Z, Pack SD, Dutra A, Pak E, Hardy J, Singleton A, Williams NM, Heutink P, Pickering-Brown S, Morris HR, Tienari PJ, Traynor BJ (2011) A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 72, 257-268.
-
(2011)
Neuron
, vol.72
, pp. 257-268
-
-
Renton, A.E.1
Majounie, E.2
Waite, A.3
Simon-Sanchez, J.4
Rollinson, S.5
Gibbs, J.R.6
Schymick, J.C.7
Laaksovirta, H.8
Van Swieten, J.C.9
Myllykangas, L.10
Kalimo, H.11
Paetau, A.12
Abramzon, Y.13
Remes, A.M.14
Kaganovich, A.15
Scholz, S.W.16
Duckworth, J.17
Ding, J.18
Harmer, D.W.19
Hernandez, D.G.20
Johnson, J.O.21
Mok, K.22
Ryten, M.23
Trabzuni, D.24
Guerreiro, R.J.25
Orrell, R.W.26
Neal, J.27
Murray, A.28
Pearson, J.29
Jansen, I.E.30
Sondervan, D.31
Seelaar, H.32
Blake, D.33
Young, K.34
Halliwell, N.35
Callister, J.B.36
Toulson, G.37
Richardson, A.38
Gerhard, A.39
Snowden, J.40
Mann, D.41
Neary, D.42
Nalls, M.A.43
Peuralinna, T.44
Jansson, L.45
Isoviita, V.M.46
Kaivorinne, A.L.47
Holtta-Vuori, M.48
Ikonen, E.49
Sulkava, R.50
Benatar, M.51
Wuu, J.52
Chio, A.53
Restagno, G.54
Borghero, G.55
Sabatelli, M.56
Italsgen, T.57
Heckerman, D.58
Rogaeva, E.59
Zinman, L.60
Rothstein, J.D.61
Sendtner, M.62
Drepper, C.63
Eichler, E.E.64
Alkan, C.65
Abdullaev, Z.66
Pack, S.D.67
Dutra, A.68
Pak, E.69
Hardy, J.70
Singleton, A.71
Williams, N.M.72
Heutink, P.73
Pickering-Brown, S.74
Morris, H.R.75
Tienari, P.J.76
Traynor, B.J.77
more..
-
7
-
-
80054832080
-
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
-
Dejesus-Hernandez M, Mackenzie IR, Boeve BF, Boxer AL, Baker M, Rutherford NJ, Nicholson AM, Finch NA, Flynn H, Adamson J, Kouri N, Wojtas A, Sengdy P, Hsiung GY, Karydas A, Seeley WW, Josephs KA, Coppola G, Geschwind DH, Wszolek ZK, Feldman H, Knopman DS, Petersen RC, Miller BL, Dickson DW, Boylan KB, Graff-Radford NR, Rademakers R (2011) Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 72, 245-256.
-
(2011)
Neuron
, vol.72
, pp. 245-256
-
-
Dejesus-Hernandez, M.1
MacKenzie, I.R.2
Boeve, B.F.3
Boxer, A.L.4
Baker, M.5
Rutherford, N.J.6
Nicholson, A.M.7
Finch, N.A.8
Flynn, H.9
Adamson, J.10
Kouri, N.11
Wojtas, A.12
Sengdy, P.13
Hsiung, G.Y.14
Karydas, A.15
Seeley, W.W.16
Josephs, K.A.17
Coppola, G.18
Geschwind, D.H.19
Wszolek, Z.K.20
Feldman, H.21
Knopman, D.S.22
Petersen, R.C.23
Miller, B.L.24
Dickson, D.W.25
Boylan, K.B.26
Graff-Radford, N.R.27
Rademakers, R.28
more..
-
8
-
-
65449161780
-
2009 Alzheimer's disease facts and figures
-
Alzheimer's Association
-
Alzheimer's Association (2009) 2009 Alzheimer's disease facts and figures. Alzheimers Dement 5, 234-270.
-
(2009)
Alzheimers Dement
, vol.5
, pp. 234-270
-
-
-
9
-
-
70350618915
-
Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic mild cognitive impairment converted to Alzheimer's disease
-
Carecchio M, Fenoglio C, De Riz M, Guidi I, Comi C, Cortini F, Venturelli E, Restelli I, Cantoni C, Bresolin N, Monaco F, Scarpini E, Galimberti D (2009) Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic mild cognitive impairment converted to Alzheimer's disease. J Neurol Sci 287, 291-293.
-
(2009)
J Neurol Sci
, vol.287
, pp. 291-293
-
-
Carecchio, M.1
Fenoglio, C.2
De Riz, M.3
Guidi, I.4
Comi, C.5
Cortini, F.6
Venturelli, E.7
Restelli, I.8
Cantoni, C.9
Bresolin, N.10
Monaco, F.11
Scarpini, E.12
Galimberti, D.13
-
10
-
-
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 RC, Dickson DW, Younkin SG, Deramecourt V, Crook J, Graff-Radford NR, Rademakers R (2009) Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members. Brain 132, 583-591.
-
(2009)
Brain
, vol.132
, 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
-
11
-
-
35348872039
-
Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
-
DOI 10.1001/archneur.64.10.1436
-
Brouwers N, Nuytemans K, van der Zee J, Gijselinck I, Engelborghs S, Theuns J, Kumar-Singh S, Pickut BA, Pals P, Dermaut B, Bogaerts V, De Pooter T, Serneels S, Van den Broeck M, Cuijt I, Mattheijssens M, Peeters K, Sciot R, Martin JJ, Cras P, Santens P, Vandenberghe R, De Deyn PP, Cruts M, Van Broeckhoven C, Sleegers K (2007) Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family. Arch Neurol 64, 1436-1446. (Pubitemid 47572667)
-
(2007)
Archives of Neurology
, vol.64
, Issue.10
, pp. 1436-1446
-
-
Brouwers, N.1
Nuytemans, K.2
Van Der Zee, J.3
Gijselinck, I.4
Engelborghs, S.5
Theuns, J.6
Kumar-Singh, S.7
Pickut, B.A.8
Pals, P.9
Dermaut, B.10
Bogaerts, V.11
De Pooter, T.12
Serneels, S.13
Van Den Broeck, M.14
Cuijt, I.15
Mattheijssens, M.16
Peeters, K.17
Sciot, R.18
Martin, J.-J.19
Cras, P.20
Santens, P.21
Vandenberghe, R.22
De Deyn, P.P.23
Cruts, M.24
Van Broeckhoven, C.25
Sleegers, K.26
more..
-
12
-
-
77649187519
-
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: An update
-
Mackenzie IR, Neumann M, Bigio EH, Cairns NJ, Alafuzoff I, Kril J, Kovacs GG, Ghetti B, Halliday G, Holm IE, Ince PG, Kamphorst W, Revesz T, Rozemuller AJ, Kumar-Singh S, Akiyama H, Baborie A, Spina S, Dickson DW, Trojanowski JQ, Mann DM (2010) Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: An update. Acta Neuropathol 119, 1-4.
-
(2010)
Acta Neuropathol
, vol.119
, pp. 1-4
-
-
MacKenzie, I.R.1
Neumann, M.2
Bigio, E.H.3
Cairns, N.J.4
Alafuzoff, I.5
Kril, J.6
Kovacs, G.G.7
Ghetti, B.8
Halliday, G.9
Holm, I.E.10
Ince, P.G.11
Kamphorst, W.12
Revesz, T.13
Rozemuller, A.J.14
Kumar-Singh, S.15
Akiyama, H.16
Baborie, A.17
Spina, S.18
Dickson, D.W.19
Trojanowski, J.Q.20
Mann, D.M.21
more..
-
13
-
-
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, Boeve B, Baker M, Adamson J, Crook R, Melquist S, Kuntz K, Petersen R, Josephs K, Pickering-Brown SM, Graff-Radford N, Uitti R, Dickson D, Wszolek Z, Gonzalez J, Beach TG, Bigio E, Johnson N, Weintraub S, Mesulam M, White CL 3rd, Woodruff B, Caselli R, Hsiung GY, Feldman H, Knopman D, Hutton M, Rademakers R (2006) Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. Hum Mol Genet 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..
-
14
-
-
33750599059
-
Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia
-
DOI 10.1093/brain/awl267
-
Snowden JS, Pickering-Brown SM, Mackenzie IR, Richardson AM, Varma A, Neary D, Mann DM (2006) Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia. Brain 129, 3091-3102. (Pubitemid 44684528)
-
(2006)
Brain
, vol.129
, Issue.11
, pp. 3091-3102
-
-
Snowden, J.S.1
Pickering-Brown, S.M.2
Mackenzie, I.R.3
Richardson, A.M.T.4
Varma, A.5
Neary, D.6
Mann, D.M.A.7
-
15
-
-
33750576830
-
Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome
-
DOI 10.1093/brain/awl276
-
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 syndrome. Brain 129, 3115-3123. (Pubitemid 44684530)
-
(2006)
Brain
, vol.129
, Issue.11
, 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
-
16
-
-
34447098853
-
Progranulin null mutations in both sporadic and familial frontotemporal dementia
-
DOI 10.1002/humu.20520
-
Le Ber I, van der Zee J, Hannequin D, Gijselinck I, Campion D, Puel M, Laquerriere A, De Pooter T, Camuzat A, Van den Broeck M, Dubois B, Sellal F, Lacomblez L, Vercelletto M, Thomas-Anterion C, Michel BF, Golfier V, Didic M, Salachas F, Duyckaerts C, Cruts M, Verpillat P, Van Broeckhoven C, Brice A, French Research Network on FTD/FTD-MND (2007) Progranulin null mutations in both sporadic and familial frontotemporal dementia. Hum Mutat 28, 846-855. (Pubitemid 47579934)
-
(2007)
Human Mutation
, vol.28
, Issue.9
, pp. 846-855
-
-
Le Ber, I.1
Van Der Zee, J.2
Hannequin, D.3
Gijselinck, U.4
Campion, D.5
Puel, M.6
Laquerriere, A.7
De Pooter, T.8
Camuzat, A.9
Van Den Broeck, M.10
Dubois, B.11
Sellal, F.12
Lacomblez, L.13
Vercelletto, M.14
Thomas-Anterion, C.15
Michel, B.-F.16
Golfier, V.17
Didic, M.18
Salachas, F.19
Duyckaerts, C.20
Cruts, M.21
Verpillat, P.22
Van Broeckhoven, C.23
Brice, A.24
Clerget-Darpoux, F.25
Defer, G.26
Desnuelle, C.27
Pasquier, F.28
Camu, W.29
more..
-
17
-
-
54449085260
-
Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration
-
Ghidoni R, Benussi L, Glionna M, Franzoni M, Binetti G (2008) Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration. Neurology 71, 1235-1239.
-
(2008)
Neurology
, vol.71
, pp. 1235-1239
-
-
Ghidoni, R.1
Benussi, L.2
Glionna, M.3
Franzoni, M.4
Binetti, G.5
-
18
-
-
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 PP, Robberecht W, Van Broeckhoven C (2009) Serum biomarker for progranulin- associated frontotemporal lobar degeneration. Ann Neurol 65, 603-609.
-
(2009)
Ann Neurol
, vol.65
, 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
-
19
-
-
78649796826
-
Low serum progranulin predicts the presence of mutations: A prospective study
-
Schofield EC, Halliday GM, Kwok J, Loy C, Double KL, Hodges JR (2010) Low serum progranulin predicts the presence of mutations: A prospective study. J Alzheimers Dis 22, 981-984.
-
(2010)
J Alzheimers Dis
, vol.22
, pp. 981-984
-
-
Schofield, E.C.1
Halliday, G.M.2
Kwok, J.3
Loy, C.4
Double, K.L.5
Hodges, J.R.6
-
20
-
-
78651365273
-
A novel progranulin mutation causing frontotemporal lobar degeneration with heterogeneous phenotypic expression
-
Rossi G, Piccoli E, Benussi L, Caso F, Redaelli V, Magnani G, Binetti G, Ghidoni R, Perani D, Giaccone G, Tagliavini F (2011) A novel progranulin mutation causing frontotemporal lobar degeneration with heterogeneous phenotypic expression. J Alzheimers Dis 23, 7-12.
-
(2011)
J Alzheimers Dis
, vol.23
, pp. 7-12
-
-
Rossi, G.1
Piccoli, E.2
Benussi, L.3
Caso, F.4
Redaelli, V.5
Magnani, G.6
Binetti, G.7
Ghidoni, R.8
Perani, D.9
Giaccone, G.10
Tagliavini, F.11
-
21
-
-
79956142378
-
The diagnosis of dementia due to Alzheimer's disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease
-
McKhann GM, Knopman DS, Chertkow H, Hyman BT, Jack CR Jr, Kawas CH, Klunk WE, Koroshetz WJ, Manly JJ, Mayeux R, Mohs RC, Morris JC, Rossor MN, Scheltens P, Carrillo MC, Thies B, Weintraub S, Phelps CH (2011) The diagnosis of dementia due to Alzheimer's disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease. Alzheimers Dement 7, 263-269.
-
(2011)
Alzheimers Dement
, vol.7
, pp. 263-269
-
-
McKhann, G.M.1
Knopman, D.S.2
Chertkow, H.3
Hyman, B.T.4
Jack Jr., C.R.5
Kawas, C.H.6
Klunk, W.E.7
Koroshetz, W.J.8
Manly, J.J.9
Mayeux, R.10
Mohs, R.C.11
Morris, J.C.12
Rossor, M.N.13
Scheltens, P.14
Carrillo, M.C.15
Thies, B.16
Weintraub, S.17
Phelps, C.H.18
-
22
-
-
6844255860
-
Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease
-
DOI 10.1093/hmg/7.1.43
-
Cruts M, van Duijn CM, Backhovens H, Van den Broeck M, Wehnert A, Serneels S, Sherrington R, Hutton M, Hardy J, St George-Hyslop PH, Hofman A, Van Broeckhoven C (1998) Estimation of the genetic contribution of presenilin-1 and-2 mutations in a population-based study of presenile Alzheimer disease. Hum Mol Genet 7, 43-51. (Pubitemid 28040736)
-
(1998)
Human Molecular Genetics
, vol.7
, Issue.1
, pp. 43-51
-
-
Cruts, M.1
Van Duijn, C.M.2
Backhovens, H.3
Van Den Broeck, M.4
Wehnert, A.5
Serneels, S.6
Sherrington, R.7
Hutton, M.8
Hardy, J.9
St George-Hyslop, P.H.10
Hofman, A.11
Van Broeckhoven, C.12
-
23
-
-
0026088977
-
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
-
Goate A, Chartier-Harlin MC, Mullan M, Brown J, Crawford F, Fidani L, Giuffra L, Haynes A, Irving N, James L (1991) Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature 349, 704-706. (Pubitemid 21912142)
-
(1991)
Nature
, vol.349
, Issue.6311
, pp. 704-706
-
-
Goate, A.1
Chartier-Harlin, M.-C.2
Mullan, M.3
Brown, J.4
Crawford, F.5
Fldani, L.6
Giuffra, L.7
Haynes, A.8
Irving, N.9
James, L.10
Mant, R.11
Newton, P.12
Rooke, K.13
Roques, P.14
Talbot, C.15
Pericak-Vance, M.16
Roses, A.17
Williamson, R.18
Rossor, M.19
Owen, M.20
Hardy, J.21
more..
-
24
-
-
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, Hasegawa M, Stevens M, Tibben A, Niermeijer MF, Hillebrand M, Ravid R, Oostra BA, Goedert M, van Duijn CM, Heutink P (1999) High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands. Am J Hum Genet 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
-
25
-
-
6344219507
-
Clinical and genetic features of human prion diseases in Catalonia: 1993-2002
-
DOI 10.1111/j.1468-1331.2004.00967.x
-
Sanchez-Valle R, Nos C, Yague J, Graus F, Dominguez A, Saiz A, Catalan Collaborative Study Group forCJD (2004) Clinical and genetic features of human prion diseases in Catalonia: 1993-2002. Eur J Neurol 11, 649-655. (Pubitemid 39389665)
-
(2004)
European Journal of Neurology
, vol.11
, Issue.10
, pp. 649-655
-
-
Sanchez-Valle, R.1
Nos, C.2
Yague, J.3
Graus, F.4
Dominguez, A.5
Saiz, A.6
-
26
-
-
79955930875
-
Different profiles of Alzheimer's disease cerebrospinal fluid biomarkers in controls and subjects with subjective memory complaints
-
Antonell A, Fortea J, Rami L, Bosch B, Balasa M, Sanchez-Valle R, Iranzo A, Molinuevo JL, Llado A (2010) Different profiles of Alzheimer's disease cerebrospinal fluid biomarkers in controls and subjects with subjective memory complaints. J Neural Transm 118, 259-262.
-
(2010)
J Neural Transm
, vol.118
, pp. 259-262
-
-
Antonell, A.1
Fortea, J.2
Rami, L.3
Bosch, B.4
Balasa, M.5
Sanchez-Valle, R.6
Iranzo, A.7
Molinuevo, J.L.8
Llado, A.9
-
27
-
-
77952477706
-
Inter-laboratory variation in cerebrospinal fluid biomarkers for Alzheimer's disease: United we stand, divided we fall
-
Mattsson N, Blennow K, ZetterbergH (2010) Inter-laboratory variation in cerebrospinal fluid biomarkers for Alzheimer's disease: United we stand, divided we fall. Clin Chem Lab Med 48, 603-607.
-
(2010)
Clin Chem Lab Med
, vol.48
, pp. 603-607
-
-
Mattsson, N.1
Blennow, K.2
Zetterberg, H.3
-
28
-
-
84858997674
-
Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: A multicenter Italian study
-
Ghidoni R, Stoppani E, Rossi G, Piccoli E, Albertini V, Paterlini A, Glionna M, Pegoiani E, Agnati LF, Fenoglio C, Scarpini E, Galimberti D, Morbin M, Tagliavini F, Binetti G, Benussi L (2012) Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: A multicenter Italian study. Neurodegener Dis 9, 121-127.
-
(2012)
Neurodegener Dis
, vol.9
, pp. 121-127
-
-
Ghidoni, R.1
Stoppani, E.2
Rossi, G.3
Piccoli, E.4
Albertini, V.5
Paterlini, A.6
Glionna, M.7
Pegoiani, E.8
Agnati, L.F.9
Fenoglio, C.10
Scarpini, E.11
Galimberti, D.12
Morbin, M.13
Tagliavini, F.14
Binetti, G.15
Benussi, L.16
-
29
-
-
48949093046
-
Gene expression study on peripheral blood identifies progranulin mutations
-
Coppola G, Karydas A, Rademakers R, Wang Q, Baker M, Hutton M, Miller BL, GeschwindDH (2008) Gene expression study on peripheral blood identifies progranulin mutations. Ann Neurol 64, 92-96.
-
(2008)
Ann Neurol
, vol.64
, pp. 92-96
-
-
Coppola, G.1
Karydas, A.2
Rademakers, R.3
Wang, Q.4
Baker, M.5
Hutton, M.6
Miller, B.L.7
Geschwind, D.H.8
-
30
-
-
45049084534
-
Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease
-
Rovelet-Lecrux A, Deramecourt V, Legallic S, Maurage CA, Le Ber I, Brice A, Lambert JC, Frebourg T, Hannequin D, Pasquier F, Campion D (2008) Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease. Neurobiol Dis 31, 41-45.
-
(2008)
Neurobiol Dis
, vol.31
, pp. 41-45
-
-
Rovelet-Lecrux, A.1
Deramecourt, V.2
Legallic, S.3
Maurage, C.A.4
Le Ber, I.5
Brice, A.6
Lambert, J.C.7
Frebourg, T.8
Hannequin, D.9
Pasquier, F.10
Campion, D.11
-
31
-
-
55249086715
-
Progranulin variability has no major role in Parkinson disease genetic etiology
-
Nuytemans K, Pals P, Sleegers K, Engelborghs S, Corsmit E, Peeters K, Pickut B, Mattheijssens M, Cras P, De Deyn PP, Theuns J, Van Broeckhoven C (2008) Progranulin variability has no major role in Parkinson disease genetic etiology. Neurology 71, 1147-1151.
-
(2008)
Neurology
, vol.71
, pp. 1147-1151
-
-
Nuytemans, K.1
Pals, P.2
Sleegers, K.3
Engelborghs, S.4
Corsmit, E.5
Peeters, K.6
Pickut, B.7
Mattheijssens, M.8
Cras, P.9
De Deyn, P.P.10
Theuns, J.11
Van Broeckhoven, C.12
-
32
-
-
39749135522
-
Phenotype variability in progranulin mutation carriers: A clinical, neuropsychological, imaging and genetic study
-
DOI 10.1093/brain/awn012
-
Le Ber I, Camuzat A, Hannequin D, Pasquier F, Guedj E, Rovelet-Lecrux A, Hahn-Barma V, van der Zee J, Clot F, Bakchine S, Puel M, Ghanim M, Lacomblez L, Mikol J, Deramecourt V, Lejeune P, de la Sayette V, Belliard S, Vercelletto M, Meyrignac C, Van Broeckhoven C, Lambert JC, Verpillat P, Campion D, Habert MO, Dubois B, Brice A, French research network on FTD/FTD-MND (2008) Phenotype variability in progranulin mutation carriers: A clinical, neuropsychological, imaging and genetic study. Brain 131, 732-746. (Pubitemid 351294727)
-
(2008)
Brain
, vol.131
, Issue.3
, pp. 732-746
-
-
Le Ber, I.1
Camuzat, A.2
Hannequin, D.3
Pasquier, F.4
Guedj, E.5
Rovelet-Lecrux, A.6
Hahn-Barma, V.7
Van Der Zee, J.8
Clot, F.9
Bakchine, S.10
Puel, M.11
Ghanim, M.12
Lacomblez, L.13
Mikol, J.14
Deramecourt, V.15
Lejeune, P.16
De La Sayette, V.17
Belliard, S.18
Vercelletto, M.19
Meyrignac, C.20
Van Broeckhoven, C.21
Lambert, J.-C.22
Verpillat, P.23
Campion, D.24
Habert, M.-O.25
Dubois, B.26
Brice, A.27
Clerget-Darpoux, F.28
Didic, M.29
Desnuelle, C.30
Duyckaerts, C.31
Golfier, V.32
Michel, B.F.33
Thomas-Anterion, C.34
Salachas, F.35
Sellal, F.36
Camu, W.37
more..
-
33
-
-
52449110477
-
Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease
-
Brouwers N, Sleegers K, Engelborghs S, Maurer-Stroh S, Gijselinck I, van der Zee J, Pickut BA, Van den Broeck M, Mattheijssens M, Peeters K, Schymkowitz J, Rousseau F, Martin JJ, Cruts M, De Deyn PP, Van Broeckhoven C (2008) Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease. Neurology 71, 656-664.
-
(2008)
Neurology
, vol.71
, pp. 656-664
-
-
Brouwers, N.1
Sleegers, K.2
Engelborghs, S.3
Maurer-Stroh, S.4
Gijselinck, I.5
Van Der Zee, J.6
Pickut, B.A.7
Van Den Broeck, M.8
Mattheijssens, M.9
Peeters, K.10
Schymkowitz, J.11
Rousseau, F.12
Martin, J.J.13
Cruts, M.14
De Deyn, P.P.15
Van Broeckhoven, C.16
-
34
-
-
67849123734
-
Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia
-
Bernardi L, Tomaino C, Anfossi M, Gallo M, Geracitano S, Costanzo A, Colao R, Puccio G, Frangipane F, Curcio SA, Mirabelli M, Smirne N, Iapaolo D, Maletta RG, Bruni AC (2009) Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia. Neurobiol Aging 30, 1825-1833.
-
(2009)
Neurobiol Aging
, vol.30
, pp. 1825-1833
-
-
Bernardi, L.1
Tomaino, C.2
Anfossi, M.3
Gallo, M.4
Geracitano, S.5
Costanzo, A.6
Colao, R.7
Puccio, G.8
Frangipane, F.9
Curcio, S.A.10
Mirabelli, M.11
Smirne, N.12
Iapaolo, D.13
Maletta, R.G.14
Bruni, A.C.15
-
35
-
-
84856532493
-
Progranulin genetic screening in frontotemporal lobar degeneration patients from central Italy
-
Bagnoli S, Piaceri I, Tedde A, Piacentini S, Nannucci S, Bracco L, Sorbi S, Nacmias B (2011) Progranulin genetic screening in frontotemporal lobar degeneration patients from central Italy. Cell Mol Neurobiol 32, 13-16.
-
(2011)
Cell Mol Neurobiol
, vol.32
, pp. 13-16
-
-
Bagnoli, S.1
Piaceri, I.2
Tedde, A.3
Piacentini, S.4
Nannucci, S.5
Bracco, L.6
Sorbi, S.7
Nacmias, B.8
-
37
-
-
77649192195
-
Brain progranulin expression in GRN-associated frontotemporal lobar degeneration
-
Chen-Plotkin AS, Xiao J, Geser F, Martinez-Lage M, Grossman M, Unger T, Wood EM, Van Deerlin VM, Trojanowski JQ, Lee VM (2010) Brain progranulin expression in GRN-associated frontotemporal lobar degeneration. Acta Neuropathol 119, 111-122.
-
(2010)
Acta Neuropathol
, vol.119
, pp. 111-122
-
-
Chen-Plotkin, A.S.1
Xiao, J.2
Geser, F.3
Martinez-Lage, M.4
Grossman, M.5
Unger, T.6
Wood, E.M.7
Van Deerlin, V.M.8
Trojanowski, J.Q.9
Lee, V.M.10
-
38
-
-
33847654643
-
Progranulin in frontotemporal lobar degeneration and neuroinflammation
-
Ahmed Z, Mackenzie IR, Hutton ML, Dickson DW (2007) Progranulin in frontotemporal lobar degeneration and neuroinflammation. J Neuroinflammatio 4, 7.
-
(2007)
J Neuroinflammatio
, vol.4
, pp. 7
-
-
Ahmed, Z.1
MacKenzie, I.R.2
Hutton, M.L.3
Dickson, D.W.4
|