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CHMP2B mutations are not a common cause of frontotemporal lobar degenerationCANNON, Ashley; BAKER, Matthew; NEARY, David et al.Neuroscience letters. 2006, Vol 398, Num 1-2, pp 83-84, issn 0304-3940, 2 p.Article

Clinicopathological and genetic correlates of frontotemporal lobar degeneration and corticobasal degenerationLLADO, Albert; SANCHEZ-VALLE, Raquel; REY, Maria Jesus et al.Journal of neurology. 2008, Vol 255, Num 4, pp 488-494, issn 0340-5354, 7 p.Article

TDP-43 gene analysis in frontotemporal lobar degenerationROLLINSON, Sara; SNOWDEN, Julie S; NEARY, David et al.Neuroscience letters. 2007, Vol 419, Num 1, pp 1-4, issn 0304-3940, 4 p.Article

No association of PGRN 3'UTR rs5848 in frontotemporal lobar degenerationROLLINSON, Sara; ROHRER, Jonathan D; PICKERING-BROWN, Stuart M et al.Neurobiology of aging. 2011, Vol 32, Num 4, pp 754-755, issn 0197-4580, 2 p.Article

MAPT gene duplications are not a cause of frontotemporal lobar degenerationLLADO, A; RODRFGUEZ -SANTIAGO, B; ANTONELL, A et al.Neuroscience letters. 2007, Vol 424, Num 1, pp 61-65, issn 0304-3940, 5 p.Article

Novel splicing mutation in the progranulin gene causing familial corticobasal syndromeMASELLIS, Mario; MOMENI, Parastoo; BLACK, Sandra et al.Brain. 2006, Vol 129, pp 3115-3123, issn 0006-8950, 9 p., 11Article

Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?VENTURELLI, Eliana; VILLA, Chiara; FUMAGALLI, Giorgio et al.Neuroscience letters. 2010, Vol 482, Num 3, pp 240-244, issn 0304-3940, 5 p.Article

Frontotemporal lobar degeneration: current knowledge and future challengesCERAMI, Chiara; SCARPINI, Elio; CAPPA, Stefano F et al.Journal of neurology. 2012, Vol 259, Num 11, pp 2278-2286, issn 0340-5354, 9 p.Article

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degenerationSEELAAR, Harro; KLIJNSMA, Kirsten Y; KONING, Inge De et al.Journal of neurology. 2010, Vol 257, Num 5, pp 747-753, issn 0340-5354, 7 p.Article

A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathiesLASHLEY, Tammaryn; ROHRER, Jonathan D; KING, Andrew et al.Brain. 2011, Vol 134, pp 2548-2564, issn 0006-8950, 17 p., 9Article

A belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD. CommentaryHARDY, John; MOMENI, Parastoo; CAEKEBEKE, Jo et al.Brain. 2006, Vol 129, issn 0006-8950, 830-831,841-852 [14 p.], 4Article

Structural anatomy of empathy in neurodegenerative diseaseRANKIN, Katherine P; GORNO-TEMPINI, Maria Luisa; ALLISON, Stephen C et al.Brain. 2006, Vol 129, pp 2945-2956, issn 0006-8950, 12 p., 11Article

TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohortVAN DER ZEE, Julie; VAN LANGENHOVE, Tim; MATTHEIJSSENS, Maria et al.Brain. 2011, Vol 134, pp 808-815, issn 0006-8950, 8 p., 3Article

Nuclear import impairment causes cytoplasmic trans-activation response DNA-binding protein accumulation and is associated with frontotemporal lobar degenerationNISHIMURA, Agnes L; ZUPUNSKI, Vera; TROAKES, Claire et al.Brain. 2010, Vol 133, pp 1763-1771, issn 0006-8950, 9 p., 6Article

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin geneMACKENZIE, Ian R. A; BAKER, Matt; FELDMAN, Howard H et al.Brain. 2006, Vol 129, pp 3081-3090, issn 0006-8950, 10 p., 11Article

Review: Recent progress in frontotemporal lobar degenerationPICKERING-BROWN, S. M.Neuropathology and applied neurobiology (Print). 2010, Vol 36, Num 1, pp 4-16, issn 0305-1846, 13 p.Article

Update on Recent Molecular and Genetic Advances in Frontotemporal Lobar DegenerationBIGIO, Eileen H.Journal of neuropathology and experimental neurology. 2008, Vol 67, Num 7, pp 635-648, issn 0022-3069, 14 p.Article

Losing protein in the brain: The case of progranulinGHIDONI, Roberta; PATERLINI, Anna; ALBERTINI, Valentina et al.Brain research. 2012, Vol 1476, pp 172-182, issn 0006-8993, 11 p.Article

Characterization of ubiquitinated intraneuronal inclusions in a novel belgian frontotemporal lobar degeneration familyPIRICI, Daniel; VANDENBERGHE, Rik; VAN BROECKHOVEN, Christine et al.Journal of neuropathology and experimental neurology. 2006, Vol 65, Num 3, pp 289-301, issn 0022-3069, 13 p.Article

Establishing short-term prognosis in Frontotemporal Lobar Degeneration spectrum: Role of genetic background and clinical phenotypeBORRONI, Barbara; GRASSI, Mario; AGOSTI, Chiara et al.Neurobiology of aging. 2010, Vol 31, Num 2, pp 270-279, issn 0197-4580, 10 p.Article

Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degenerationROLLINSON, Sara; RIZZU, Patrizia; MEAD, Simon et al.Neurobiology of aging. 2009, Vol 30, Num 4, pp 656-665, issn 0197-4580, 10 p.Article

TAR DNA-Binding Protein 43 Immunohistochemistry Reveals Extensive Neuritic Pathology in FTLD-U : A Midwest-Southwest Consortium for FTLD StudyHATANPAA, Kimmo J; BIGIO, Eileen H; WHITE, Charles L et al.Journal of neuropathology and experimental neurology. 2008, Vol 67, Num 4, pp 271-279, issn 0022-3069, 9 p.Article

Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43 -negative neuronal inclusionsMACKENZIE, Ian R. A; FOTI, Dean; WOULFE, John et al.Brain. 2008, Vol 131, pp 1282-1293, issn 0006-8950, 12 p., 5Article

What the left and right anterior fusiform gyri tell us about semantic memoryMION, Marco; PATTERSON, Karalyn; ACOSTA-CABRONERO, Julio et al.Brain. 2010, Vol 133, pp 3256-3268, issn 0006-8950, 13 p., 11Article