Ubiquitin‐positive inclusions and progression of pathology in frontotemporal dementia and motor neurone disease identifies a group with mainly early pathology
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J. Hodges | J. Hodges | J. Xuereb | T. Bak | J. Kril | R. Pamphlett | C. Kersaitis | G. Halliday
[1] Karalyn Patterson,et al. The pathological basis of semantic dementia. , 2005, Brain : a journal of neurology.
[2] J. Kril,et al. Distribution of brain atrophy in behavioral variant frontotemporal dementia , 2005, Journal of the Neurological Sciences.
[3] J. Kril,et al. Staging disease severity in movement disorder tauopathies: Brain atrophy separates progressive supranuclear palsy from corticobasal degeneration , 2005, Movement disorders : official journal of the Movement Disorder Society.
[4] K. Kosaka,et al. Ubiquitin and ubiquitin‐related proteins in the brains of patients with atypical Pick's disease without Pick bodies and dementia with motor neuron disease , 2004, Neuropathology : official journal of the Japanese Society of Neuropathology.
[5] S. Al-Sarraj,et al. Morphological differences of intraneuronal ubiquitin‐positive inclusions in the dentate gyrus and parahippocampal gyrus of motor neuron disease with dementia , 2004, Neuropathology : official journal of the Japanese Society of Neuropathology.
[6] J. Kril,et al. Regional and cellular pathology in frontotemporal dementia: relationship to stage of disease in cases with and without Pick bodies , 2004, Acta Neuropathologica.
[7] E. Bigio,et al. Frontotemporal lobar degeneration with motor neuron disease-type inclusions predominates in 76 cases of frontotemporal degeneration , 2004, Acta Neuropathologica.
[8] J. Hodges,et al. Clinicopathological correlates in frontotemporal dementia , 2004, Annals of neurology.
[9] M N Rossor,et al. Frontotemporal lobar degeneration and ubiquitin immunohistochemistry , 2004, Neuropathology and applied neurobiology.
[10] M. Mesulam,et al. Neuronal Ubiquitinated Intranuclear Inclusions in Familial and Non‐Familial Frontotemporal Dementia of the Motor Neuron Disease Type Associated with Amyotrophic Lateral Sclerosis , 2004, Journal of neuropathology and experimental neurology.
[11] D. Dickson,et al. Hippocampal Sclerosis and Ubiquitin-Positive Inclusions in Dementia Lacking Distinctive Histopathology , 2004, Dementia and Geriatric Cognitive Disorders.
[12] J. Kril,et al. Clinicopathological Staging of Frontotemporal Dementia Severity: Correlation with Regional Atrophy , 2004, Dementia and Geriatric Cognitive Disorders.
[13] S. Landau,et al. Cortical selective vulnerability in motor neuron disease: a morphometric study. , 2004, Brain : a journal of neurology.
[14] C. Bouras,et al. Cortical ubiquitin-positive inclusions in frontotemporal dementia without motor neuron disease: a quantitative immunocytochemical study , 2004, Acta Neuropathologica.
[15] C. Duyckaerts,et al. Amyotrophic lateral sclerosis with neuronal intranuclear protein inclusions , 2004, Acta Neuropathologica.
[16] Mari Yoshida,et al. Amyotrophic lateral sclerosis with dementia: The clinicopathological spectrum , 2004, Neuropathology : official journal of the Japanese Society of Neuropathology.
[17] K. Kosaka,et al. Ubiquitin and ubiquitin‐related proteins in neurons and dendrites of brains of atypical Pick's disease without Pick bodies , 2004, Neuropathology (Kyoto. 1993).
[18] S. Hirai,et al. Ubiquitin-positive intraneuronal inclusions in the extramotor cortices of presenile dementia patients with motor neuron disease , 1992, Journal of Neurology.
[19] J. Hodges,et al. Survival in frontotemporal dementia , 2003, Neurology.
[20] D. Dickson,et al. Frontotemporal and motor neurone degeneration with neurofilament inclusion bodies: additional evidence for overlap between FTD and ALS , 2003, Neuropathology and applied neurobiology.
[21] L. Stefanis,et al. Ubiquitinated inclusions and neuronal cell death. , 2003, Histology and histopathology.
[22] J. Kril,et al. Severity of gliosis in Pick's disease and frontotemporal lobar degeneration: tau-positive glia differentiate these disorders. , 2003, Brain : a journal of neurology.
[23] J. Hodges,et al. Staging disease severity in pathologically confirmed cases of frontotemporal dementia , 2003, Neurology.
[24] H. Feldman,et al. Neuronal intranuclear inclusions distinguish familial FTD-MND type from sporadic cases , 2003, Acta Neuropathologica.
[25] B Miller,et al. Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease. , 2001, Archives of neurology.
[26] Andrew Kertesz,et al. Frontotemporal dementia with ubiquitinated cytoplasmic and intranuclear inclusions , 2001, Acta Neuropathologica.
[27] A. Kakita,et al. Ubiquitinated neuronal inclusions in the neostriatum in patients with amyotrophic lateral sclerosis with and without dementia--a study of 60 patients 31 to 87 years of age. , 2001, Clinical neuropathology.
[28] T D Bird,et al. Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions , 2000, Neurology.
[29] B. Pakkenberg,et al. Unchanged total number of neurons in motor cortex and neocortex in amyotrophic lateral sclerosis: a stereological study , 2000, Journal of Neuroscience Methods.
[30] M. Figueiredo-Pereira,et al. Ubiquitin, cellular inclusions and their role in neurodegeneration , 1998, Trends in Neurosciences.
[31] J. Lowe,et al. Motor neurone disease-inclusion dementia. , 1996, Neurodegeneration : a journal for neurodegenerative disorders, neuroprotection, and neuroregeneration.
[32] N. Cairns,et al. Involvement of the amygdala, dentate and hippocampus in motor neuron disease , 1995, Journal of the Neurological Sciences.
[33] I. Nakano. Temporal Lobe Lesions in Amyotrophic Lateral Sclerosis with or without Dementia: A Neuropathological Study , 1993 .
[34] D. Neary,et al. Hippocampal and neocortical ubiquitin-immunoreactive inclusions in amyotrophic lateral sclerosis with dementia , 1992, Neuroscience Letters.
[35] D. Dickson,et al. Ubiquitin immunoreactive structures in normal human brains. Distribution and developmental aspects. , 1990, Laboratory investigation; a journal of technical methods and pathology.