-
1
-
-
34247597966
-
The Frontal Behavioural Inventory (Italian version) differentiates frontotemporal lobar degeneration variants from Alzheimer's disease
-
Alberici A., Geroldi C., Cotelli M., Adorni A., Calabria M., Rossi G., Borroni B., Padovani A., Zanetti O., Kertesz A. The Frontal Behavioural Inventory (Italian version) differentiates frontotemporal lobar degeneration variants from Alzheimer's disease. Neurol. Sci 2007, 28:80-86.
-
(2007)
Neurol. Sci
, vol.28
, pp. 80-86
-
-
Alberici, A.1
Geroldi, C.2
Cotelli, M.3
Adorni, A.4
Calabria, M.5
Rossi, G.6
Borroni, B.7
Padovani, A.8
Zanetti, O.9
Kertesz, A.10
-
2
-
-
0035205278
-
Why voxel-based morphometry should be used
-
Ashburner J., Friston K.J. Why voxel-based morphometry should be used. Neuroimage 2001, 14:1238-1243.
-
(2001)
Neuroimage
, vol.14
, pp. 1238-1243
-
-
Ashburner, J.1
Friston, K.J.2
-
4
-
-
33746919083
-
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
-
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.
-
(2006)
Nature
, vol.442
, 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
-
-
0000398777
-
Revised administration and scoring of the digit PNFAn test
-
Blackburn H.L., Benton A.L. Revised administration and scoring of the digit PNFAn test. J. Consult. Psychol 1957, 21:139-143.
-
(1957)
J. Consult. Psychol
, vol.21
, pp. 139-143
-
-
Blackburn, H.L.1
Benton, A.L.2
-
6
-
-
39749141572
-
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series
-
Beck J., Rohrer J.D., Campbell T., Isaacs A., Morrison K.E., Goodall E.F., Warrington E.K., Stevens J., Revesz T., Holton J., Al-Sarraj S., King A., Scahill R., Warren J.D., Fox N.C., Rossor M.N., Collinge J., Mead S. A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series. Brain 2008, 131:706-720.
-
(2008)
Brain
, vol.131
, pp. 706-720
-
-
Beck, J.1
Rohrer, J.D.2
Campbell, T.3
Isaacs, A.4
Morrison, K.E.5
Goodall, E.F.6
Warrington, E.K.7
Stevens, J.8
Revesz, T.9
Holton, J.10
Al-Sarraj, S.11
King, A.12
Scahill, R.13
Warren, J.D.14
Fox, N.C.15
Rossor, M.N.16
Collinge, J.17
Mead, S.18
-
7
-
-
84946640033
-
Raven's Progressive Matrices: construct validity
-
Bingham W.C., Burke H.R., Murray S. Raven's Progressive Matrices: construct validity. J. Psychol 1966, 62:205-209.
-
(1966)
J. Psychol
, vol.62
, pp. 205-209
-
-
Bingham, W.C.1
Burke, H.R.2
Murray, S.3
-
8
-
-
0029166541
-
Functional connectivity in the motor cortex of resting human brain using echo-planar MRI
-
Biswal B., Yetkin F.Z., Haughton V.M., Hyde J.S. Functional connectivity in the motor cortex of resting human brain using echo-planar MRI. Magn. Reson. Med 1995, 34:537-541.
-
(1995)
Magn. Reson. Med
, vol.34
, pp. 537-541
-
-
Biswal, B.1
Yetkin, F.Z.2
Haughton, V.M.3
Hyde, J.S.4
-
9
-
-
46449123028
-
Brain magnetic resonance imaging structural changes in a pedigree of asymptomatic progranulin mutation carriers
-
Borroni B., Alberici A., Premi E., Archetti S., Garibotto V., Agosti C., Gasparotti R., Di Luca M., Perani D., Padovani A. Brain magnetic resonance imaging structural changes in a pedigree of asymptomatic progranulin mutation carriers. Rejuvenation Res 2008, 11:585-595.
-
(2008)
Rejuvenation Res
, vol.11
, pp. 585-595
-
-
Borroni, B.1
Alberici, A.2
Premi, E.3
Archetti, S.4
Garibotto, V.5
Agosti, C.6
Gasparotti, R.7
Di Luca, M.8
Perani, D.9
Padovani, A.10
-
10
-
-
46149083470
-
Progranulin genetic variations in frontotemporal lobar degeneration: evidence for low mutation frequency in an Italian clinical series
-
Borroni B., Archetti S., Alberici A., Agosti C., Gennarelli M., Bigni B., Bonvicini C., Ferrari M., Bellelli G., Galimberti D., Scarpini E., Di Lorenzo D., Caimi L., Caltagirone C., Di Luca M., Padovani A. Progranulin genetic variations in frontotemporal lobar degeneration: evidence for low mutation frequency in an Italian clinical series. Neurogenetics 2008, 9:197-205.
-
(2008)
Neurogenetics
, vol.9
, pp. 197-205
-
-
Borroni, B.1
Archetti, S.2
Alberici, A.3
Agosti, C.4
Gennarelli, M.5
Bigni, B.6
Bonvicini, C.7
Ferrari, M.8
Bellelli, G.9
Galimberti, D.10
Scarpini, E.11
Di Lorenzo, D.12
Caimi, L.13
Caltagirone, C.14
Di Luca, M.15
Padovani, A.16
-
11
-
-
79952899795
-
Founder effect and estimation of the age of the Progranulin Thr272fs mutation in 14 Italian pedigrees with frontotemporal lobar degeneration
-
Borroni B., Bonvicini C., Galimberti D., Tremolizzo L., Papetti A., Archetti S., Turla M., Alberici A., Agosti C., Premi E., Appollonio I., Rainero I., Ferrarese C., Gennarelli M., Scarpini E., Padovani A. Founder effect and estimation of the age of the Progranulin Thr272fs mutation in 14 Italian pedigrees with frontotemporal lobar degeneration. Neurobiol. Aging 2011, 32:555.e1-555.e8.
-
(2011)
Neurobiol. Aging
, vol.32
-
-
Borroni, B.1
Bonvicini, C.2
Galimberti, D.3
Tremolizzo, L.4
Papetti, A.5
Archetti, S.6
Turla, M.7
Alberici, A.8
Agosti, C.9
Premi, E.10
Appollonio, I.11
Rainero, I.12
Ferrarese, C.13
Gennarelli, M.14
Scarpini, E.15
Padovani, A.16
-
12
-
-
79958788915
-
Genetic background predicts poor prognosis in frontotemporal lobar degeneration
-
Borroni B., Grassi M., Archetti S., Papetti A., Del Bo R., Bonvicini C., Comi G.P., Gennarelli M., Bellelli G., Di Luca M., Padovani A. Genetic background predicts poor prognosis in frontotemporal lobar degeneration. Neurodegener. Dis 2011, 8:289-295.
-
(2011)
Neurodegener. Dis
, vol.8
, pp. 289-295
-
-
Borroni, B.1
Grassi, M.2
Archetti, S.3
Papetti, A.4
Del Bo, R.5
Bonvicini, C.6
Comi, G.P.7
Gennarelli, M.8
Bellelli, G.9
Di Luca, M.10
Padovani, A.11
-
13
-
-
48549085645
-
Brain volumetrics to investigate aging and the principal forms of degenerative cognitive decline: a brief review
-
Bozzali M., Cercignani M., Caltagirone C. Brain volumetrics to investigate aging and the principal forms of degenerative cognitive decline: a brief review. Magn. Reson. Imaging 2008, 26:1065-1070.
-
(2008)
Magn. Reson. Imaging
, vol.26
, pp. 1065-1070
-
-
Bozzali, M.1
Cercignani, M.2
Caltagirone, C.3
-
14
-
-
33746910649
-
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
-
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.
-
(2006)
Nature
, vol.442
, 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..
-
15
-
-
41249089087
-
Loss of progranulin function in frontotemporal lobar degeneration
-
Cruts M., Van Van Broeckhoven C. Loss of progranulin function in frontotemporal lobar degeneration. Trends Genet 2008, 24:186-194.
-
(2008)
Trends Genet
, vol.24
, pp. 186-194
-
-
Cruts, M.1
Van Van Broeckhoven, C.2
-
16
-
-
0027985334
-
The Neuropsychiatric Inventory: comprehensive assessment of psychopathology in dementia
-
Cummings J.L., Mega M., Gray K., Rosenberg-Thompson S., Carusi D.A., Gornbein J. The Neuropsychiatric Inventory: comprehensive assessment of psychopathology in dementia. Neurology 1994, 44:2308-2314.
-
(1994)
Neurology
, vol.44
, pp. 2308-2314
-
-
Cummings, J.L.1
Mega, M.2
Gray, K.3
Rosenberg-Thompson, S.4
Carusi, D.A.5
Gornbein, J.6
-
17
-
-
31844433315
-
FMRI resting state networks define distinct modes of long-distance interactions in the human brain
-
De Luca M., Beckmann C.F., De Stefano N., Matthews P.M., Smith S.M. fMRI resting state networks define distinct modes of long-distance interactions in the human brain. Neuroimage 2006, 29:1359-1367.
-
(2006)
Neuroimage
, vol.29
, pp. 1359-1367
-
-
De Luca, M.1
Beckmann, C.F.2
De Stefano, N.3
Matthews, P.M.4
Smith, S.M.5
-
18
-
-
28244471573
-
Blood oxygenation level dependent contrast resting state networks are relevant to functional activity in the neocortical sensorimotor system
-
De Luca M., Smith S., De Stefano N., Federico A., Matthews P.M. Blood oxygenation level dependent contrast resting state networks are relevant to functional activity in the neocortical sensorimotor system. Exp. Brain Res 2005, 167:587-594.
-
(2005)
Exp. Brain Res
, vol.167
, pp. 587-594
-
-
De Luca, M.1
Smith, S.2
De Stefano, N.3
Federico, A.4
Matthews, P.M.5
-
19
-
-
73649175004
-
The Token Test: a sensitive test to detect receptive disturbances in aphasics
-
De Renzi E., Vignolo L.A. The Token Test: a sensitive test to detect receptive disturbances in aphasics. Brain 1962, 85:665-678.
-
(1962)
Brain
, vol.85
, pp. 665-678
-
-
De Renzi, E.1
Vignolo, L.A.2
-
20
-
-
0016823810
-
"Mini-Mental State". A practical method for grading the cognitive state of patients for the clinician
-
Folstein M.F., Folstein S.E., McHugh P.R. "Mini-Mental State". A practical method for grading the cognitive state of patients for the clinician. J. Psychiatr. Res 1975, 12:189-198.
-
(1975)
J. Psychiatr. Res
, vol.12
, pp. 189-198
-
-
Folstein, M.F.1
Folstein, S.E.2
McHugh, P.R.3
-
21
-
-
34548014282
-
Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging
-
Fox M.D., Raichle M.E. Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging. Nat. Rev. Neurosci 2007, 8:700-711.
-
(2007)
Nat. Rev. Neurosci
, vol.8
, pp. 700-711
-
-
Fox, M.D.1
Raichle, M.E.2
-
22
-
-
0035199224
-
Dementia and neurodevelopmental predisposition: cognitive dysfunction in presymptomatic subjects precedes dementia by decades in frontotemporal dementia
-
Geschwind D.H., Robidoux J., Alarcón M., Miller B.L., Wilhelmsen K.C., Cummings J.L., Nasreddine Z.S. Dementia and neurodevelopmental predisposition: cognitive dysfunction in presymptomatic subjects precedes dementia by decades in frontotemporal dementia. Ann. Neurol 2001, 50:741-746.
-
(2001)
Ann. Neurol
, vol.50
, pp. 741-746
-
-
Geschwind, D.H.1
Robidoux, J.2
Alarcón, M.3
Miller, B.L.4
Wilhelmsen, K.C.5
Cummings, J.L.6
Nasreddine, Z.S.7
-
23
-
-
78650487445
-
Regional brain atrophy and functional disconnection across Alzheimer's disease evolution
-
Gili T., Cercignani M., Serra L., Perri R., Giove F., Maraviglia B., Caltagirone C., Bozzali M. Regional brain atrophy and functional disconnection across Alzheimer's disease evolution. J. Neurol. Neurosurg., Psychiatry 2011, 82:58-66.
-
(2011)
J. Neurol. Neurosurg., Psychiatry
, vol.82
, pp. 58-66
-
-
Gili, T.1
Cercignani, M.2
Serra, L.3
Perri, R.4
Giove, F.5
Maraviglia, B.6
Caltagirone, C.7
Bozzali, M.8
-
24
-
-
33645078169
-
Comparison of family histories in FTLD subtypes and related tauopathies
-
Goldman J.S., Farmer J.M., Wood E.M., Johnson J.K., Boxer A., Neuhaus J., Lomen-Hoerth C., Wilhelmsen K.C., Lee V.M., Grossman M., Miller B.L. Comparison of family histories in FTLD subtypes and related tauopathies. Neurology 2005, 65:1817-1819.
-
(2005)
Neurology
, vol.65
, pp. 1817-1819
-
-
Goldman, J.S.1
Farmer, J.M.2
Wood, E.M.3
Johnson, J.K.4
Boxer, A.5
Neuhaus, J.6
Lomen-Hoerth, C.7
Wilhelmsen, K.C.8
Lee, V.M.9
Grossman, M.10
Miller, B.L.11
-
25
-
-
1442329321
-
Cognition and anatomy in three variants of primary progressive aphasia
-
Gorno-Tempini M.L., Dronkers N.F., Rankin K.P., Ogar J.M., Phengrasamy L., Rosen H.J., Johnson J.K., Weiner M.W., Miller B.L. Cognition and anatomy in three variants of primary progressive aphasia. Ann. Neurol 2004, 55:335-346.
-
(2004)
Ann. Neurol
, vol.55
, pp. 335-346
-
-
Gorno-Tempini, M.L.1
Dronkers, N.F.2
Rankin, K.P.3
Ogar, J.M.4
Phengrasamy, L.5
Rosen, H.J.6
Johnson, J.K.7
Weiner, M.W.8
Miller, B.L.9
-
26
-
-
79952823979
-
Classification of primary progressive aphasia and its variants
-
Gorno-Tempini M.L., Hillis A.E., Weintraub S., Kertesz A., Mendez M., Cappa S.F., Ogar J.M., Rohrer J.D., Black S., Boeve B.F., Manes F., Dronkers N.F., Vandenberghe R., Rascovsky K., Patterson K., Miller B.L., Knopman D.S., Hodges J.R., Mesulam M.M., Grossman M. Classification of primary progressive aphasia and its variants. Neurology 2011, 76:1006-1014.
-
(2011)
Neurology
, vol.76
, pp. 1006-1014
-
-
Gorno-Tempini, M.L.1
Hillis, A.E.2
Weintraub, S.3
Kertesz, A.4
Mendez, M.5
Cappa, S.F.6
Ogar, J.M.7
Rohrer, J.D.8
Black, S.9
Boeve, B.F.10
Manes, F.11
Dronkers, N.F.12
Vandenberghe, R.13
Rascovsky, K.14
Patterson, K.15
Miller, B.L.16
Knopman, D.S.17
Hodges, J.R.18
Mesulam, M.M.19
Grossman, M.20
more..
-
27
-
-
0037422586
-
Functional connectivity in the resting brain: a network analysis of the default mode hypothesis
-
Greicius M.D., Krasnow B., Reiss A.L., Menon V. Functional connectivity in the resting brain: a network analysis of the default mode hypothesis. Proc. Natl. Acad. Sci. U. S. A. 2003, 100:253-258.
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, pp. 253-258
-
-
Greicius, M.D.1
Krasnow, B.2
Reiss, A.L.3
Menon, V.4
-
28
-
-
1842427969
-
Default-mode network activity distinguishes Alzheimer's disease from healthy aging: Evidence from functional MRI
-
Greicius M.D., Srivastava G., Reiss A.L., Menon V. Default-mode network activity distinguishes Alzheimer's disease from healthy aging: Evidence from functional MRI. Proc. Natl. Acad. Sci. U. S. A. 2004, 101:4637-4642.
-
(2004)
Proc. Natl. Acad. Sci. U. S. A.
, vol.101
, pp. 4637-4642
-
-
Greicius, M.D.1
Srivastava, G.2
Reiss, A.L.3
Menon, V.4
-
29
-
-
0032543684
-
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17
-
Hutton M., Lendon C.L., 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 5'-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 1998, 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..
-
30
-
-
0015677794
-
The Set test as an aid to the detection of dementia in old people
-
Isaacs B., Kennie A.T. The Set test as an aid to the detection of dementia in old people. Br. J. Psychiatry 1973, 123:467-470.
-
(1973)
Br. J. Psychiatry
, vol.123
, pp. 467-470
-
-
Isaacs, B.1
Kennie, A.T.2
-
31
-
-
78651299905
-
Increased caspase activation and decreased TDP-43 solubility in progranulin knockout cortical cultures
-
Kleinberger G., Wils H., Ponsaerts P., Joris G., Timmermans J.P., Van Broeckhoven C., Kumar-Singh S. Increased caspase activation and decreased TDP-43 solubility in progranulin knockout cortical cultures. J. Neurochem 2010, 115:735-747.
-
(2010)
J. Neurochem
, vol.115
, pp. 735-747
-
-
Kleinberger, G.1
Wils, H.2
Ponsaerts, P.3
Joris, G.4
Timmermans, J.P.5
Van Broeckhoven, C.6
Kumar-Singh, S.7
-
32
-
-
0014579432
-
Assessment of older people: self-maintaining and instrumental activities of daily living
-
Lawton M.P., Brody E.M. Assessment of older people: self-maintaining and instrumental activities of daily living. Gerontologist 1969, 9:179-186.
-
(1969)
Gerontologist
, vol.9
, pp. 179-186
-
-
Lawton, M.P.1
Brody, E.M.2
-
33
-
-
39749135522
-
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study
-
French Research Network on FTD/FTD-MND
-
LeBer 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 J.C., Verpillat P., Campion D., Habert M.O., Dubois B., Brice A. Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study. Brain 2008, 131:732-746. French Research Network on FTD/FTD-MND.
-
(2008)
Brain
, vol.131
, pp. 732-746
-
-
LeBer, 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
more..
-
34
-
-
0025376402
-
Psychometric construction of the Rey-Osterrieth Complex Figure: methodological considerations and interrater reliability
-
Loring D.W., Martin R.C., Meador K.J., Lee G.P. Psychometric construction of the Rey-Osterrieth Complex Figure: methodological considerations and interrater reliability. Arch. Clin. Neuropsychol 1990, 5:1-14.
-
(1990)
Arch. Clin. Neuropsychol
, vol.5
, pp. 1-14
-
-
Loring, D.W.1
Martin, R.C.2
Meador, K.J.3
Lee, G.P.4
-
35
-
-
33750576830
-
Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome
-
Masellis M., Momeni P., Meschino W., Heffner R., Elder J., Sato C., Liang Y., St George-Hyslop P., Hardy J., Bilbao J., Black S., Rogaeva E. Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome. Brain 2006, 129:3115-3123.
-
(2006)
Brain
, vol.129
, pp. 3115-3123
-
-
Masellis, M.1
Momeni, P.2
Meschino, W.3
Heffner, 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
-
36
-
-
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 G.M., Albert M.S., Grossman M., Miller B., Dickson D., Trojanowski J.Q. 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. Work Group on Frontotemporal Dementia and Pick's Disease.
-
(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
-
37
-
-
33846094364
-
Progranulin mutations in primary progressive aphasia: the PPA1 and PPA3 families
-
Mesulam M., Johnson N., Krefft T.A., Gass J.M., Cannon A.D., Adamson J.L., Bigio E.H., Weintraub S., Dickson D.W., Hutton M.L., Graff-Radford N.R. Progranulin mutations in primary progressive aphasia: the PPA1 and PPA3 families. Arch. Neurol 2007, 64:43-47.
-
(2007)
Arch. Neurol
, vol.64
, pp. 43-47
-
-
Mesulam, M.1
Johnson, N.2
Krefft, T.A.3
Gass, J.M.4
Cannon, A.D.5
Adamson, J.L.6
Bigio, E.H.7
Weintraub, S.8
Dickson, D.W.9
Hutton, M.L.10
Graff-Radford, N.R.11
-
38
-
-
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, 51:1546-1554.
-
(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
-
39
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
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. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 2006, 314:130-133.
-
(2006)
Science
, vol.314
, 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.19
-
40
-
-
34548633862
-
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C->T (Arg493X) mutation: an international initiative
-
Rademakers R., Baker M., Gass J., Adamson J., Huey E.D., Momeni P., Spina S., Coppola G., Karydas A.M., Stewart H., Johnson N., Hsiung G.Y., Kelley B., Kuntz K., Steinbart E., Wood E.M., Yu C.E., Josephs K., Sorenson E., Womack K.B., Weintraub S., Pickering-Brown S.M., Schofield P.R., Brooks W.S., Van Deerlin V.M., Snowden J., Clark C.M., Kertesz A., Boylan K., Ghetti B., Neary D., Schellenberg G.D., Beach T.G., Mesulam M., Mann D., Grafman J., Mackenzie I.R., Feldman H., Bird T., Petersen R., Knopman D., Boeve B., Geschwind D.H., Miller B., Wszolek Z., Lippa C., Bigio E.H., Dickson D., Graff-Radford N., Hutton M. Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C->T (Arg493X) mutation: an international initiative. Lancet Neurol 2007, 6:857-868.
-
(2007)
Lancet Neurol
, vol.6
, pp. 857-868
-
-
Rademakers, R.1
Baker, M.2
Gass, J.3
Adamson, J.4
Huey, E.D.5
Momeni, P.6
Spina, S.7
Coppola, G.8
Karydas, A.M.9
Stewart, H.10
Johnson, N.11
Hsiung, G.Y.12
Kelley, B.13
Kuntz, K.14
Steinbart, E.15
Wood, E.M.16
Yu, C.E.17
Josephs, K.18
Sorenson, E.19
Womack, K.B.20
Weintraub, S.21
Pickering-Brown, S.M.22
Schofield, P.R.23
Brooks, W.S.24
Van Deerlin, V.M.25
Snowden, J.26
Clark, C.M.27
Kertesz, A.28
Boylan, K.29
Ghetti, B.30
Neary, D.31
Schellenberg, G.D.32
Beach, T.G.33
Mesulam, M.34
Mann, D.35
Grafman, J.36
Mackenzie, I.R.37
Feldman, H.38
Bird, T.39
Petersen, R.40
Knopman, D.41
Boeve, B.42
Geschwind, D.H.43
Miller, B.44
Wszolek, Z.45
Lippa, C.46
Bigio, E.H.47
Dickson, D.48
Graff-Radford, N.49
Hutton, M.50
more..
-
41
-
-
68049123562
-
Recent insights into the molecular genetics of dementia
-
Rademakers R., Rovelet-Lecrux A. Recent insights into the molecular genetics of dementia. Trends Neurosci 2009, 32:451-461.
-
(2009)
Trends Neurosci
, vol.32
, pp. 451-461
-
-
Rademakers, R.1
Rovelet-Lecrux, A.2
-
42
-
-
0000119553
-
Validity of the Trail Making Test as an indicator of organic brain damage
-
Reitan R.M. Validity of the Trail Making Test as an indicator of organic brain damage. Percept. Mot. Skills 1958, 8:271-276.
-
(1958)
Percept. Mot. Skills
, vol.8
, pp. 271-276
-
-
Reitan, R.M.1
-
43
-
-
77956227571
-
Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations
-
Rohrer J.D., Ridgway G.R., Modat M., Ourselin S., Mead S., Fox N.C., Rossor M.N., Warren J.D. Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations. Neuroimage 2010, 53:1070-1076.
-
(2010)
Neuroimage
, vol.53
, pp. 1070-1076
-
-
Rohrer, J.D.1
Ridgway, G.R.2
Modat, M.3
Ourselin, S.4
Mead, S.5
Fox, N.C.6
Rossor, M.N.7
Warren, J.D.8
-
44
-
-
64149093013
-
Neurodegenerative diseases target large-scale human brain networks
-
Seeley W.W., Crawford R.K., Zhou J., Miller B.L., Greicius M.D. Neurodegenerative diseases target large-scale human brain networks. Neuron 2009, 62:42-52.
-
(2009)
Neuron
, vol.62
, pp. 42-52
-
-
Seeley, W.W.1
Crawford, R.K.2
Zhou, J.3
Miller, B.L.4
Greicius, M.D.5
-
45
-
-
77957331866
-
Are the behavioral symptoms of Alzheimer's disease directly associated with neurodegeneration?
-
Serra L., Perri R., Cercignani M., Spanò B., Fadda L., Marra C., Carlesimo G.A., Caltagirone C., Bozzali M. Are the behavioral symptoms of Alzheimer's disease directly associated with neurodegeneration?. J. Alzheimers Dis 2010, 21:627-639.
-
(2010)
J. Alzheimers Dis
, vol.21
, pp. 627-639
-
-
Serra, L.1
Perri, R.2
Cercignani, M.3
Spanò, B.4
Fadda, L.5
Marra, C.6
Carlesimo, G.A.7
Caltagirone, C.8
Bozzali, M.9
-
46
-
-
0018361757
-
Repeatability and validity of a modified activities of daily living (ADL) index in studies of chronic disability
-
Sheikh K., Smith D.S., Meade T.W., Goldenberg E., Brennan P.J., Kinsella G. Repeatability and validity of a modified activities of daily living (ADL) index in studies of chronic disability. Int. Rehabil. Med 1979, 1:51-58.
-
(1979)
Int. Rehabil. Med
, vol.1
, pp. 51-58
-
-
Sheikh, K.1
Smith, D.S.2
Meade, T.W.3
Goldenberg, E.4
Brennan, P.J.5
Kinsella, G.6
-
47
-
-
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, 65:603-609.
-
(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
-
48
-
-
33750599059
-
Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia
-
Snowden J.S., Pickering-Brown S.M., Mackenzie I.R., Richardson A.M., Varma A., Neary D., Mann D.M. Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia. Brain 2006, 129:3091-3102.
-
(2006)
Brain
, vol.129
, pp. 3091-3102
-
-
Snowden, J.S.1
Pickering-Brown, S.M.2
Mackenzie, I.R.3
Richardson, A.M.4
Varma, A.5
Neary, D.6
Mann, D.M.7
-
49
-
-
0003374626
-
Tau protein pathology in neurodegenerative diseases
-
Spillantini M.G., Goedert M. Tau protein pathology in neurodegenerative diseases. Trends Neurosci 1998, 21:428-433.
-
(1998)
Trends Neurosci
, vol.21
, pp. 428-433
-
-
Spillantini, M.G.1
Goedert, M.2
-
51
-
-
42049087853
-
Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival
-
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, 181:37-41.
-
(2008)
J. Cell Biol
, vol.181
, 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
-
52
-
-
34447096609
-
Clinical, genetic, and pathologic characteristics of patients with frontotemporal dementia and progranulin mutations
-
Van Deerlin V.M., Wood E.M., Moore P., Yuan W., Forman M.S., Clark C.M., Neumann M., Kwong L.K., Trojanowski J.Q., Lee V.M., Grossman M. Clinical, genetic, and pathologic characteristics of patients with frontotemporal dementia and progranulin mutations. Arch. Neurol 2007, 64:1148-1153.
-
(2007)
Arch. Neurol
, vol.64
, pp. 1148-1153
-
-
Van Deerlin, V.M.1
Wood, E.M.2
Moore, P.3
Yuan, W.4
Forman, M.S.5
Clark, C.M.6
Neumann, M.7
Kwong, L.K.8
Trojanowski, J.Q.9
Lee, V.M.10
Grossman, M.11
-
53
-
-
77951921512
-
Divergent network connectivity changes in behavioural variant frontotemporal dementia and Alzheimer's disease
-
Zhou J., Greicius M.D., Gennatas E.D., Growdon M.E., Jang J.Y., Rabinovici G.D., Kramer J.H., Weiner M., Miller B.L., Seeley W.W. Divergent network connectivity changes in behavioural variant frontotemporal dementia and Alzheimer's disease. Brain 2010, 133:1352-1367.
-
(2010)
Brain
, vol.133
, pp. 1352-1367
-
-
Zhou, J.1
Greicius, M.D.2
Gennatas, E.D.3
Growdon, M.E.4
Jang, J.Y.5
Rabinovici, G.D.6
Kramer, J.H.7
Weiner, M.8
Miller, B.L.9
Seeley, W.W.10
|