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Short-term suppression of A315T mutant human TDP-43 expression improves functional deficits in a novel inducible transgenic mouse model of FTLD-TDP and ALS
Short-term suppression of A315T mutant human TDP-43 expression improves functional deficits in a novel inducible transgenic mouse model of FTLD-TDP and ALS
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Short-term suppression of A315T mutant human TDP-43 expression improves functional deficits in a novel inducible transgenic mouse model of FTLD-TDP and ALS

Ke, Yazi D. ; van Hummel, Annika ; Stevens, Claire H. ; Gladbach, Amadeus ; Ippati, Stefania ; Bi, Mian ; Lee, Wei S. ; Krüger, Sarah ; van der Hoven, Julia ; Volkerling, Alexander ; Bongers, Andre ; Halliday, Glenda ; Haass, Nikolas K. ; Kiernan, Matthew ; Delerue, Fabien ; Ittner, Lars M.

Acta neuropathologica, 2015-11, Vol.130 (5), p.661-678 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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2
FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration
FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration
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FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration

Urwin, Hazel ; Josephs, Keith A. ; Rohrer, Jonathan D. ; Mackenzie, Ian R. ; Neumann, Manuela ; Authier, Astrid ; Seelaar, Harro ; Van Swieten, John C. ; Brown, Jeremy M. ; Johannsen, Peter ; Nielsen, Jorgen E. ; Holm, Ida E. ; Dickson, Dennis W. ; Rademakers, Rosa ; Graff-Radford, Neill R. ; Parisi, Joseph E. ; Petersen, Ronald C. ; Hatanpaa, Kimmo J. ; White III, Charles L. ; Weiner, Myron F. ; Geser, Felix ; Van Deerlin, Vivianna M. ; Trojanowski, John Q. ; Miller, Bruce L. ; Seeley, William W. ; van der Zee, Julie ; Kumar-Singh, Samir ; Engelborghs, Sebastiaan ; De Deyn, Peter P. ; Van Broeckhoven, Christine ; Bigio, Eileen H. ; Deng, Han-Xiang ; Halliday, Glenda M. ; Kril, Jillian J. ; Munoz, David G. ; Mann, David M. ; Pickering-Brown, Stuart M. ; Doodeman, Valerie ; Adamson, Gary ; Ghazi-Noori, Shabnam ; Fisher, Elizabeth M. C. ; Holton, Janice L. ; Revesz, Tamas ; Rossor, Martin N. ; Collinge, John ; Mead, Simon ; Isaacs, Adrian M.

Acta neuropathologica, 2010-07, Vol.120 (1), p.33-41 [Periódico revisado por pares]

Berlin/Heidelberg: Springer-Verlag

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3
Frontotemporal dementia–amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1–q12.2: genetic, clinical and neuropathological analysis
Frontotemporal dementia–amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1–q12.2: genetic, clinical and neuropathological analysis
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Frontotemporal dementia–amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1–q12.2: genetic, clinical and neuropathological analysis

Dobson-Stone, Carol ; Luty, Agnes A. ; Thompson, Elizabeth M. ; Blumbergs, Peter ; Brooks, William S. ; Short, Cathy L. ; Field, Colin D. ; Panegyres, Peter K. ; Hecker, Jane ; Solski, Jennifer A. ; Blair, Ian P. ; Fullerton, Janice M. ; Halliday, Glenda M. ; Schofield, Peter R. ; Kwok, John B. J.

Acta neuropathologica, 2013-04, Vol.125 (4), p.523-533 [Periódico revisado por pares]

Berlin/Heidelberg: Springer-Verlag

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4
An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies
An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies
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An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies

de Silva, Rohan ; Lashley, Tammaryn ; Strand, Catherine ; Shiarli, Anna-Maria ; Shi, Jing ; Tian, Jinzhou ; Bailey, Kathryn L ; Davies, Peter ; Bigio, Eileen H ; Arima, Kunimasa ; Iseki, Eizo ; Murayama, Shigeo ; Kretzschmar, Hans ; Neumann, Manuela ; Lippa, Carol ; Halliday, Glenda ; MacKenzie, James ; Ravid, Rivka ; Dickson, Dennis ; Wszolek, Zbigniew ; Iwatsubo, Takeshi ; Pickering-Brown, Stuart M ; Holton, Janice ; Lees, Andrew ; Revesz, Tamas ; Mann, David M A

Acta neuropathologica, 2006-04, Vol.111 (4), p.329-340 [Periódico revisado por pares]

Germany: Springer Nature B.V

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5
Consensus neuropathological diagnosis of common dementia syndromes: testing and standardising the use of multiple diagnostic criteria
Consensus neuropathological diagnosis of common dementia syndromes: testing and standardising the use of multiple diagnostic criteria
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Consensus neuropathological diagnosis of common dementia syndromes: testing and standardising the use of multiple diagnostic criteria

HALLIDAY, G ; NG, T ; KALNINS, R ; MASTERS, C. L ; MCLEAN, C ; MILDER, D. G ; PAMPHLETT, R ; SCOTT, G ; TANNENBERG, A ; KRIL, J ; RODRIGUEZ, M ; HARDING, A ; BLUMBERGS, P ; EVANS, W ; FABIAN, V ; FRYER, J ; GONZALES, M ; HARPER, C

Acta neuropathologica, 2002-07, Vol.104 (1), p.72-78 [Periódico revisado por pares]

Berlin: Springer

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6
Ubiquitin-positive achromatic neurons in corticobasal degeneration
Ubiquitin-positive achromatic neurons in corticobasal degeneration
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Ubiquitin-positive achromatic neurons in corticobasal degeneration

HALLIDAY, G. M ; DAVIES, L ; MCRITCHIE, D. A ; CARTWRIGHT, H ; PAMPHLETT, R ; MORRIS, J. G. L

Acta neuropathologica, 1995-07, Vol.90 (1), p.68-75 [Periódico revisado por pares]

Berlin: Springer

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7
Analysis of staining methods for different cortical plaques in Alzheimer's disease
Analysis of staining methods for different cortical plaques in Alzheimer's disease
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Analysis of staining methods for different cortical plaques in Alzheimer's disease

Halliday, G ; Flowers, D ; Baum, L

Acta neuropathologica, 1994-02, Vol.87 (2), p.174-186 [Periódico revisado por pares]

Germany

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8
Congenital absence of pyramids and its significance in genetic diseases
Congenital absence of pyramids and its significance in genetic diseases
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Congenital absence of pyramids and its significance in genetic diseases

CHOW, C. W ; HALLIDAY, J. L ; ANDERSON, R. McD ; DANKS, D. M ; FORTUNE, D. W

Acta neuropathologica, 1985-01, Vol.65 (3-4), p.313-317 [Periódico revisado por pares]

Berlin: Springer

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