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Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
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Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia.
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Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
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TDP-43 pathology and neuronal loss in amyotrophic lateral sclerosis spinal cord.
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Sequential distribution of pTDP-43 pathology in behavioral variant frontotemporal dementia (bvFTD).
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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
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Diffusion tensor imaging analysis of sequential spreading of disease in amyotrophic lateral sclerosis confirms patterns of TDP-43 pathology.
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Amyotrophic lateral sclerosis.
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Amyotrophic lateral sclerosis.
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Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study.
Adriano Chiò, Andrea Calvo, Cristina Moglia, Letizia Mazzini, Gabriele Mora. J Neurol Neurosurg Psychiatry 2011
Adriano Chiò, Andrea Calvo, Cristina Moglia, Letizia Mazzini, Gabriele Mora. J Neurol Neurosurg Psychiatry 2011
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Evidence of widespread cerebral microglial activation in amyotrophic lateral sclerosis: an [11C](R)-PK11195 positron emission tomography study.
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Classification of primary progressive aphasia and its variants.
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A harmonized classification system for FTLD-TDP pathology.
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Structural brain correlates of cognitive and behavioral impairment in MND.
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The frontotemporal dementia-motor neuron disease continuum.
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A large-scale multicentre cerebral diffusion tensor imaging study in amyotrophic lateral sclerosis.
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Screening for cognition and behaviour changes in ALS.
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TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis.
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Basal ganglia pathology in ALS is associated with neuropsychological deficits.
Judith Machts, Kristian Loewe, Joern Kaufmann, Sibylle Jakubiczka, Susanne Abdulla, Susanne Petri, Reinhard Dengler, Hans-Jochen Heinze, Stefan Vielhaber, Mircea Ariel Schoenfeld,[...]. Neurology 2015
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Hippocampal pathology in amyotrophic lateral sclerosis: selective vulnerability of subfields and their associated projections.
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The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study.
Julie Phukan, Marwa Elamin, Peter Bede, Norah Jordan, Laura Gallagher, Susan Byrne, Catherine Lynch, Niall Pender, Orla Hardiman. J Neurol Neurosurg Psychiatry 2012
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Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
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Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6.
Caroline Vance, Boris Rogelj, Tibor Hortobágyi, Kurt J De Vos, Agnes Lumi Nishimura, Jemeen Sreedharan, Xun Hu, Bradley Smith, Deborah Ruddy, Paul Wright,[...]. Science 2009
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Imaging the pathoanatomy of amyotrophic lateral sclerosis in vivo: targeting a propagation-based biological marker.
Jan Kassubek, Hans-Peter Müller, Kelly Del Tredici, Dorothée Lulé, Martin Gorges, Heiko Braak, Albert C Ludolph. J Neurol Neurosurg Psychiatry 2018
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Amyotrophic lateral sclerosis.
Orla Hardiman, Ammar Al-Chalabi, Adriano Chio, Emma M Corr, Giancarlo Logroscino, Wim Robberecht, Pamela J Shaw, Zachary Simmons, Leonard H van den Berg. Nat Rev Dis Primers 2017
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Multimodal longitudinal study of structural brain involvement in amyotrophic lateral sclerosis.
Hannelore K van der Burgh, Henk-Jan Westeneng, Renée Walhout, Kevin van Veenhuijzen, Harold H G Tan, Jil M Meier, Leonhard A Bakker, Jeroen Hendrikse, Michael A van Es, Jan H Veldink,[...]. Neurology 2020
Hannelore K van der Burgh, Henk-Jan Westeneng, Renée Walhout, Kevin van Veenhuijzen, Harold H G Tan, Jil M Meier, Leonhard A Bakker, Jeroen Hendrikse, Michael A van Es, Jan H Veldink,[...]. Neurology 2020
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Patient-derived frontotemporal lobar degeneration brain extracts induce formation and spreading of TDP-43 pathology in vivo.
Sílvia Porta, Yan Xu, Clark R Restrepo, Linda K Kwong, Bin Zhang, Hannah J Brown, Edward B Lee, John Q Trojanowski, Virginia M-Y Lee. Nat Commun 2018
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Expansion of the classification of FTLD-TDP: distinct pathology associated with rapidly progressive frontotemporal degeneration.
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The validation of the Italian Edinburgh Cognitive and Behavioural ALS Screen (ECAS).
Barbara Poletti, Federica Solca, Laura Carelli, Fabiana Madotto, Annalisa Lafronza, Andrea Faini, Alessia Monti, Stefano Zago, Daniela Calini, Cinzia Tiloca,[...]. Amyotroph Lateral Scler Frontotemporal Degener 2016
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The two-year progression of structural and functional cerebral MRI in amyotrophic lateral sclerosis.
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Cognitive correlates in amyotrophic lateral sclerosis: a population-based study in Italy.
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Basal ganglia involvement in amyotrophic lateral sclerosis.
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Connectivity-based characterisation of subcortical grey matter pathology in frontotemporal dementia and ALS: a multimodal neuroimaging study.
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ALS-specific cognitive and behavior changes associated with advancing disease stage in ALS.
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Iron accumulation in deep cortical layers accounts for MRI signal abnormalities in ALS: correlating 7 tesla MRI and pathology.
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The phenotypic variability of amyotrophic lateral sclerosis.
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Brainstem pathology in amyotrophic lateral sclerosis and primary lateral sclerosis: A longitudinal neuroimaging study.
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Prion-like properties of pathological TDP-43 aggregates from diseased brains.
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Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
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Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.
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Cognitive phenotypes of sequential staging in amyotrophic lateral sclerosis.
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Corpus callosum involvement is a consistent feature of amyotrophic lateral sclerosis.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.