Neurofibrillary tangle-predominant dementia: comparison with classical Alzheimer disease
暂无分享,去创建一个
[1] Douglas Walker,et al. Hippocampal Sclerosis Dementia with Tauopathy , 2003, Brain pathology.
[2] H. Akiyama,et al. Different immunoreactivities of the microtubule-binding region of tau and its molecular basis in brains from patients with Alzheimer's disease, Pick's disease, progressive supranuclear palsy and corticobasal degeneration , 2003, Acta Neuropathologica.
[3] Charles Duyckaerts,et al. Beta A4 deposits are constant in the brain of the oldest old: an immunocytochemical study of 20 French centenarians. , 1993, Neurobiology of aging.
[4] B. Hyman,et al. Transcriptional and conformational changes of the tau molecule in Alzheimer's disease. , 2005, Biochimica et biophysica acta.
[5] A. Delacourte,et al. Two‐Dimensional Characterization of Paired Helical Filament‐Tau from Alzheimer's Disease: Demonstration of an Additional 74‐kDa Component and Age‐Related Biochemical Modifications , 1997, Journal of neurochemistry.
[6] A. Probst,et al. Apolipoprotein E genotype in senile dementia with tangles differs from Alzheimer's disease , 2003, Neuropathology and applied neurobiology.
[7] D. Graham,et al. High frequency of apolipoprotein E ϵ2 Allele in hemorrhage due to cerebral amyloid angiopathy , 1997, Annals of neurology.
[8] Ronald C. Petersen,et al. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 , 1998, Nature.
[9] K. Jellinger,et al. Age-related electrical status epilepticus during sleep and epileptic negative myoclonus in DRPLA , 2006, Neurology.
[10] D. Dickson,et al. Increased Frequency of Argyrophilic Grain Disease in Alzheimer Disease with 4R Tau-Specific Immunohistochemistry , 2005, Journal of neuropathology and experimental neurology.
[11] Masahito Yamada,et al. Risk Factors for Cerebral Amyloid Angiopathy in the Elderly , 2002, Annals of the New York Academy of Sciences.
[12] A. Delacourte,et al. Alzheimer’s disease: a true tauopathy fueled by amyloid precursor protein dysfunction , 2005 .
[13] M. L. Schmidt,et al. Autosomal dominant dementia with widespread neurofibrillary tangles , 1997, Annals of neurology.
[14] G. Getz,et al. Association of human, rat, and rabbit apolipoprotein E with β‐amyloid , 1997, Journal of neuroscience research.
[15] J. Haines,et al. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. , 1993, Science.
[16] John X. Morris,et al. Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17. , 1998, Science.
[17] H. Braak,et al. Neuropathological stageing of Alzheimer-related changes , 2004, Acta Neuropathologica.
[18] C. Duyckaerts. Atypical Parkinsonian Disorders , 2005 .
[19] John Q. Trojanowski,et al. The neuropathology of dementia , 2004 .
[20] E. Otomo,et al. Senile Dementia of the Neurofibrillary Tangle Type: A Comparison with Alzheimer’s Disease , 2001, Dementia and Geriatric Cognitive Disorders.
[21] A. M. Saunders,et al. Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease , 1994, Nature Genetics.
[22] H. Braak,et al. Staging of Alzheimer disease-associated neurofibrillary pathology using paraffin sections and immunocytochemistry , 2006, Acta Neuropathologica.
[23] A. Delacourte,et al. Tau pathology: a marker of neurodegenerative disorders , 2000, Current opinion in neurology.
[24] Masanori Kato,et al. Clinical Aspects of ‘Senile Dementia of the Tangle Type’ – A Subset of Dementia in the Senium Separable from Late-Onset Alzheimer’s Disease , 1998, Dementia and Geriatric Cognitive Disorders.
[25] B. Hyman,et al. Apolipoprotein E in sporadic Alzheimer's disease: Allelic variation and receptor interactions , 1993, Neuron.
[26] D. Dickson,et al. Neurodegenerative disorders with extensive tau pathology: A comparative study and review , 1996, Annals of neurology.
[27] P. Davies,et al. Hippocampal sclerosis: a common pathological feature of dementia in very old (≥80 years of age) humans , 2004, Acta Neuropathologica.
[28] John Q Trojanowski,et al. Transgenic animal models of tauopathies. , 2005, Biochimica et biophysica acta.
[29] T. Erkinjuntti,et al. [Aging and dementia]. , 1985, Duodecim; laaketieteellinen aikakauskirja.
[30] H. Brewer,et al. Amyloid-associated proteins α1-antichymotrypsin and apolipoprotein E promote assembly of Alzheimer β-protein into filaments , 1994, Nature.
[31] K. Manton,et al. Apolipoprotein E genotype determines survival in the oldest old (85 years or older) who have good cognition. , 1996, Archives of neurology.
[32] K. Jellinger,et al. Senile Dementia with Tangles (Tangle Predominant Form of Senile Dementia) , 1998, Brain pathology.
[33] B. Hyman,et al. Region-specific dissociation of neuronal loss and neurofibrillary pathology in a mouse model of tauopathy. , 2006, The American journal of pathology.
[34] A. Lees,et al. Dementia with Lewy bodies from the perspective of tauopathy , 2003, Acta Neuropathologica.
[35] T. Tokuda,et al. Thorn-shaped astrocytes: possibly secondarily induced tau-positive glial fibrillary tangles , 2004, Acta Neuropathologica.
[36] K. Jellinger,et al. Alzheimer Pathology in the olfactory bulb , 2005, Neuropathology and applied neurobiology.
[37] M. Tolnay,et al. Argyrophilic grain disease: A late‐onset dementia with distinctive features among tauopathies , 2004, Neuropathology : official journal of the Japanese Society of Neuropathology.
[38] K. Jellinger,et al. Neurofibrillary tangle predominant form of senile dementia of Alzheimer type: a rare subtype in very old subjects , 2004, Acta Neuropathologica.
[39] M. Goedert,et al. Argyrophilic grain disease: widespread hyperphosphorylation of tau protein in limbic neurons , 1997, Acta Neuropathologica.
[40] H. Akiyama,et al. Immunohistochemical investigation of neurofibrillary tangles and their tau isoforms in brains of limbic neurofibrillary tangle dementia , 2006, Neuroscience Letters.
[41] K. Jellinger,et al. Tau and α-synuclein brainstem pathology in Alzheimer disease: relation with extrapyramidal signs , 2006, Acta Neuropathologica.
[42] K. Jellinger,et al. O2-01-04 Tau and alpha-synuclein brainstem pathology in Alzheimer disease , 2006, Alzheimer's & Dementia.
[43] T. Iwaki,et al. Quantitative analysis of neurofibrillary pathology in a general population to reappraise neuropathological criteria for senile dementia of the neurofibrillary tangle type (tangle‐only dementia): The Hisayama study , 2006, Neuropathology : official journal of the Japanese Society of Neuropathology.
[44] H. Akiyama,et al. A subset of senile dementia with high incidence of the apolipoprotein E epsilon2 allele. , 1997, Annals of neurology.
[45] J. Trojanowski,et al. Biochemical analysis of tau proteins in argyrophilic grain disease, Alzheimer's disease, and Pick's disease : a comparative study. , 2002, The American journal of pathology.
[46] D W Dickson,et al. Widespread cytoskeletal pathology characterizes corticobasal degeneration. , 1995, The American journal of pathology.
[47] Patrick R. Hof,et al. Functional neurobiology of aging , 2001 .
[48] T. Mizutani,et al. Neuropathological background of twenty-seven centenarian brains , 1992, Journal of the Neurological Sciences.
[49] K. Iqbal,et al. Alzheimer's disease : biology, diagnosis, and therapeutics , 1996 .
[50] Y. Nakazato,et al. Histopathological and immunohistochemical study of the enteric innervations among various types of aganglionoses including isolated and syndromic Hirschsprung disease , 2006, Neuropathology : official journal of the Japanese Society of Neuropathology.
[51] Pl Lantos,et al. Greenfield's Neuropathology , 1985 .
[52] B. Crain,et al. Interlaboratory Comparison of Neuropathology Assessments in Alzheimer's Disease: A Study of the Consortium to Establish a Registry for Alzheimer's Disease (CERAD) , 1994, Journal of neuropathology and experimental neurology.
[53] I. Litvan. ATYPICAL PARKINSONIAN DISORDERS , 2004 .
[54] T. Tabira,et al. FTDP‐17 mutations N279K and S305N in tau produce increased splicing of exon 10 , 1999, FEBS letters.
[55] H. Akiyama,et al. A subset of senile dementia with high incidence of the apolipoprotein E ϵ2 allele , 1997 .
[56] P. Hof,et al. Quantitative immunohistochemical analysis of the distribution of neurofibrillary tangles and senile plaques in the cerebral cortex of nonagenarians and centenarians , 2004, Acta Neuropathologica.
[57] D. Dickson,et al. An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies , 2006, Acta Neuropathologica.
[58] K. Jellinger,et al. Low prevalence of apolipoprotein E ε4 allele in the neurofibrillary tangle predominant form of senile dementia , 1997, Acta Neuropathologica.
[59] M. Yamada. Senile dementia of the neurofibrillary tangle type (tangle‐only dementia): Neuropathological criteria and clinical guidelines for diagnosis * , 2003, Neuropathology : official journal of the Japanese Society of Neuropathology.
[60] T. Hanihara,et al. Corticobasal degeneration: widespread argentophilic threads and glia in addition to neurofibrillary tangles. Similarities of cytoskeletal abnormalities in corticobasal degeneration and progressive supranuclear palsy , 1996, Journal of the Neurological Sciences.
[61] A. Fisher,et al. Progress in Alzheimer’s and Parkinson’s Diseases , 1998, Advances in Behavioral Biology.
[62] J. Holton,et al. Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule‐binding repeat domains as demonstrated by new specific monoclonal antibodies , 2003, Neuropathology and applied neurobiology.
[63] D. Dickson,et al. Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders: Dickson/Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders , 2011 .
[64] A. Delacourte,et al. Argyrophilic grain disease and Alzheimer's disease are distinguished by their different distribution of tau protein isoforms , 2002, Acta Neuropathologica.
[65] J. Miller,et al. Neuropathological indexes of Alzheimer's disease in demented and nondemented persons aged 80 years and older. , 1993, Archives of neurology.
[66] E. Otomo,et al. An immunohistochemical study of centenarian brains: a comparison , 1998, Journal of the Neurological Sciences.
[67] D. Dickson. Required techniques and useful molecular markers in the neuropathologic diagnosis of neurodegenerative diseases , 2005, Acta Neuropathologica.
[68] B. Hyman,et al. Association of apolipoprotein E epsilon2 and vasculopathy in cerebral amyloid angiopathy. , 1998, Neurology.
[69] K. Kosaka. Limbic neurofibrillary tangle dementia , 1997 .
[70] S. Paul,et al. Lack of apolipoprotein E dramatically reduces amyloid beta-peptide deposition. , 1997, Nature genetics.
[71] A. Fisher,et al. Alzheimer’s disease: a true tauopathy fueled by amyloid precursor protein dysfunction A Delacourte , 2005 .
[72] D. Dickson,et al. APOE E4 is a determinant for Alzheimer type pathology in progressive supranuclear palsy , 2003, Neurology.
[73] Charles Duyckaerts,et al. Subtypes and differential laminar distributions of βA4 deposits in Alzheimer's disease: relationship with the intellectual status of 26 cases , 2004, Acta Neuropathologica.
[74] T. Iwase,et al. Argyrophilic grain disease: frequency and neuropathology in centenarians , 2006, Acta Neuropathologica.
[75] P. Lantos,et al. Office of Rare Diseases Neuropathologic Criteria for Corticobasal Degeneration , 2002, Journal of neuropathology and experimental neurology.
[76] H. Braak,et al. [Post-mortem diagnosis of Alzheimer's disease]. , 2005, Der Pathologe.
[77] D. Dickson. The Neuropathology of Dementia: Sporadic tauopathies: Pick's disease, corticobasal degeneration, progressive supranuclear palsy and argyrophilic grain disease , 2004 .
[78] A. Delacourte,et al. Comparative Biochemistry of Tau in Progressive Supranuclear Palsy, Corticobasal Degeneration, FTDP‐17 and Pick's Disease , 1999, Brain pathology.
[79] S. Greenberg,et al. Association of apolipoprotein E ϵ2 and vasculopathy in cerebral amyloid angiopathy , 1998, Neurology.
[80] D. Dickson,et al. Selective Neurofibrillary Degeneration of the Hippocampal CA2 Sector Is Associated with Four‐Repeat Tauopathies , 2002, Journal of neuropathology and experimental neurology.
[81] Stefano Cappa,et al. Aging and dementia , 2001 .
[82] J. Woulfe,et al. Abnormalities of the nucleus and nuclear inclusions in neurodegenerative disease: a work in progress , 2007, Neuropathology and applied neurobiology.
[83] D. Dickson,et al. Argyrophilic Grain Disease Is a Sporadic 4‐Repeat Tauopathy , 2002, Journal of neuropathology and experimental neurology.
[84] J. Growdon,et al. No alteration in tau exon 10 alternative splicing in tangle-bearing neurons of the Alzheimer’s disease brain , 2006, Acta Neuropathologica.
[85] J. Trojanowski,et al. Biochemical Analysis of τ Proteins in Argyrophilic Grain Disease, Alzheimer's Disease, and Pick's Disease: A Comparative Study , 2002 .
[86] T. Mizutani,et al. Clinicopathologic's Investigations of Atypic's Senile Dementia of 'Szheimer Type , 1994 .
[87] K. Jellinger,et al. Incidence of cerebrovascular lesions in Alzheimer's disease: a postmortem study , 2002, Acta Neuropathologica.
[88] J. Kimura,et al. Immunocytochemical characterization of glial fibrillary tangles in Alzheimer's disease brain. , 1995, The American journal of pathology.
[89] C. Eisdorfer,et al. Early Diagnosis of Dementias , 1989 .
[90] K. Jellinger,et al. Low prevalence of apolipoprotein E epsilon 4 allele in the neurofibrillary tangle predominant form of senile dementia. , 1997, Acta neuropathologica.
[91] K. Jellinger,et al. Accumulation of abnormally phosphorylated τ precedes the formation of neurofibrillary tangles in Alzheimer's disease , 1989, Brain Research.
[92] H. Braak,et al. Postmortale Diagnosestellung bei Morbus Alzheimer , 2005, Der Pathologe.
[93] J. Ulrich. Abundant neurofibrillary tangles without senile plaques in a subset of patients with senile dementia , 1992 .
[94] A. Lees,et al. Immunohistochemical study of tau accumulation in early stages of Alzheimer-type neurofibrillary lesions , 2004, Acta Neuropathologica.
[95] D. Dickson,et al. Neuropathologic Overlap of Progressive Supranuclear Palsy, Pick's Disease and Corticobasal Degeneration , 1996, Journal of neuropathology and experimental neurology.
[96] E. Otomo,et al. Dementia of the Alzheimer type and related dementias in the aged: DAT subgroups and senile dementia of the neurofibrillary tangle type , 1996 .
[97] K. Jellinger. A View on Early Diagnosis of Dementias from Neuropathology , 2006 .
[98] I Litvan,et al. Progressive supranuclear palsy and corticobasal degeneration. , 2011 .
[99] N. Shibata,et al. Astrocytic plaques and tufts of abnormal fibers do not coexist in corticobasal degeneration and progressive supranuclear palsy , 1998, Acta Neuropathologica.