Frontotemporal lobar degeneration
暂无分享,去创建一个
[1] G. Schellenberg,et al. The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration. , 2010, Archives of neurology.
[2] M. Kiernan,et al. FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis , 2009, Journal of Neurology, Neurosurgery & Psychiatry.
[3] H. Kretzschmar,et al. A new subtype of frontotemporal lobar degeneration with FUS pathology. , 2009, Brain : a journal of neurology.
[4] I. Mackenzie,et al. Absence of FUS-immunoreactive pathology in frontotemporal dementia linked to chromosome 3 (FTD-3) caused by mutation in the CHMP2B gene , 2009, Acta Neuropathologica.
[5] D. Munoz,et al. FUS pathology in basophilic inclusion body disease , 2009, Acta Neuropathologica.
[6] B. Ghetti,et al. TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea , 2009, Movement disorders : official journal of the Movement Disorder Society.
[7] H. Kretzschmar,et al. Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease , 2009, Acta Neuropathologica.
[8] E. Kremmer,et al. Proteolytic processing of TAR DNA binding protein‐43 by caspases produces C‐terminal fragments with disease defining properties independent of progranulin , 2009, Journal of neurochemistry.
[9] P. Deyn,et al. Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS , 2009, Neurobiology of Aging.
[10] J. Neuhaus,et al. An Open-label Study of Memantine Treatment in 3 Subtypes of Frontotemporal Lobar Degeneration , 2009, Alzheimer disease and associated disorders.
[11] Hans Brunnström,et al. Prevalence of dementia subtypes: a 30-year retrospective survey of neuropathological reports. , 2009, Archives of gerontology and geriatrics.
[12] B. Dubois,et al. TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration , 2009, Annals of neurology.
[13] D. Cleveland,et al. Rethinking ALS: The FUS about TDP-43 , 2009, Cell.
[14] J L Haines,et al. Supporting Online Material Materials and Methods Figs. S1 to S7 Tables S1 to S4 References Mutations in the Fus/tls Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis , 2022 .
[15] Hans Förstl,et al. No association of TDP-43 with sporadic frontotemporal dementia , 2009, Neurobiology of Aging.
[16] D. Dickson. Neuropathologic differentiation of progressive supranuclear palsy and corticobasal degeneration , 1999, Journal of Neurology.
[17] K. Jellinger,et al. Clinical features differentiating patients with postmortem confirmed progressive supranuclear palsy and corticobasal degeneration , 1999, Journal of Neurology.
[18] K. Vossel,et al. New approaches to the treatment of frontotemporal lobar degeneration , 2008, Current opinion in neurology.
[19] J R Hodges,et al. Incidence of early-onset dementias in Cambridgeshire, United Kingdom , 2008, Neurology.
[20] Nathaniel Mercaldo,et al. Development of methodology for conducting clinical trials in frontotemporal lobar degeneration. , 2008, Brain : a journal of neurology.
[21] W. Kamphorst,et al. Distinct genetic forms of frontotemporal dementia , 2008, Neurology.
[22] J. Miklossy,et al. Enduring involvement of tau, β-amyloid, α-synuclein, ubiquitin and TDP-43 pathology in the amyotrophic lateral sclerosis/parkinsonism–dementia complex of Guam (ALS/PDC) , 2008, Acta Neuropathologica.
[23] Peter Heutink,et al. Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia , 2008, The Lancet Neurology.
[24] W. Jagust,et al. Aβ amyloid and glucose metabolism in three variants of primary progressive aphasia , 2008, Annals of neurology.
[25] A. Pestronk,et al. TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia , 2008, Journal of Neurology, Neurosurgery, and Psychiatry.
[26] J. Trojanowski,et al. Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations. , 2008, Archives of neurology.
[27] R. Petersen,et al. Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia , 2008, Human molecular genetics.
[28] Hans Förstl,et al. A 6‐month, open‐label study of memantine in patients with frontotemporal dementia , 2008, International journal of geriatric psychiatry.
[29] M. Morita,et al. Phosphorylated TDP‐43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis , 2008, Annals of neurology.
[30] William T. Hu,et al. Temporal lobar predominance of TDP-43 neuronal cytoplasmic inclusions in Alzheimer disease , 2008, Acta Neuropathologica.
[31] J. Trojanowski,et al. Enrichment of C-terminal fragments in TAR DNA-binding protein-43 cytoplasmic inclusions in brain but not in spinal cord of frontotemporal lobar degeneration and amyotrophic lateral sclerosis. , 2008, The American journal of pathology.
[32] D. Dickson,et al. Frontotemporal lobar degeneration with ubiquitin-positive, but TDP-43-negative inclusions , 2008, Acta Neuropathologica.
[33] H. Kretzschmar,et al. TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD , 2008, Acta Neuropathologica.
[34] Nancy Johnson,et al. Alzheimer and frontotemporal pathology in subsets of primary progressive aphasia , 2008, Annals of neurology.
[35] J. Trojanowski,et al. Concomitant TAR-DNA-Binding Protein 43 Pathology Is Present in Alzheimer Disease and Corticobasal Degeneration but Not in Other Tauopathies , 2008, Journal of neuropathology and experimental neurology.
[36] J. Hodges,et al. Measuring progression in frontotemporal dementia , 2008, Neurology.
[37] J. Trojanowski,et al. Variations in the progranulin gene affect global gene expression in frontotemporal lobar degeneration. , 2008, Human molecular genetics.
[38] C. Jack,et al. Abnormal TDP-43 immunoreactivity in AD modifies clinicopathologic and radiologic phenotype , 2008, Neurology.
[39] J. Trojanowski,et al. CSF biomarkers in frontotemporal lobar degeneration with known pathology , 2008, Neurology.
[40] I. Mackenzie,et al. Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43-negative neuronal inclusions. , 2008, Brain : a journal of neurology.
[41] P. Carmeliet,et al. Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival , 2008, The Journal of cell biology.
[42] C. Lomen‐Hoerth. Amyotrophic lateral sclerosis from bench to bedside. , 2008, Seminars in neurology.
[43] Rohani Omar,et al. Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene. , 2008, Archives of neurology.
[44] J. Morris,et al. TAR DNA-Binding Protein 43 Immunohistochemistry Reveals Extensive Neuritic Pathology in FTLD-U: A Midwest-Southwest Consortium for FTLD Study , 2008, Journal of neuropathology and experimental neurology.
[45] Xun Hu,et al. TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis , 2008, Science.
[46] Charles D. Smith,et al. Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia , 2008, American journal of medical genetics. Part A.
[47] J. Trojanowski,et al. New directions for frontotemporal dementia drug discovery , 2008, Alzheimer's & Dementia.
[48] D. Yves von Cramon,et al. Neural networks in frontotemporal dementia—A meta-analysis , 2008, Neurobiology of Aging.
[49] Julie S Snowden,et al. Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations. , 2008, Brain : a journal of neurology.
[50] Eric Guedj,et al. Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study. , 2008, Brain : a journal of neurology.
[51] Andrew King,et al. A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series. , 2008, Brain : a journal of neurology.
[52] C. Jack,et al. Voxel-based morphometry in autopsy proven PSP and CBD , 2008, Neurobiology of Aging.
[53] Maria Luisa Gorno-Tempini,et al. Frontal paralimbic network atrophy in very mild behavioral variant frontotemporal dementia. , 2008, Archives of neurology.
[54] A. Kertesz,et al. Galantamine in Frontotemporal Dementia and Primary Progressive Aphasia , 2008, Dementia and Geriatric Cognitive Disorders.
[55] E. Buratti,et al. Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease. , 2008, Frontiers in bioscience : a journal and virtual library.
[56] B. Miller,et al. New Genes, New Dilemmas: FTLD Genetics and Its Implications for Families , 2008, American journal of Alzheimer's disease and other dementias.
[57] B. Miller,et al. Distinct MRI Atrophy Patterns in Autopsy-Proven Alzheimer's Disease and Frontotemporal Lobar Degeneration , 2008, American journal of Alzheimer's disease and other dementias.
[58] D. Neary,et al. Imbalance of a serotonergic system in frontotemporal dementia: implication for pharmacotherapy , 2008, Psychopharmacology.
[59] T. Kikusui,et al. Alteration of behavioural phenotype in mice by targeted disruption of the progranulin gene , 2007, Behavioural Brain Research.
[60] H. Arai,et al. Concurrence of TDP-43, tau and α-synuclein pathology in brains of Alzheimer's disease and dementia with Lewy bodies , 2007, Brain Research.
[61] J. Woolley,et al. Frontotemporal dementia and mania. , 2007, The American journal of psychiatry.
[62] Jennifer Farmer,et al. Distinct antemortem profiles in patients with pathologically defined frontotemporal dementia. , 2007, Archives of neurology.
[63] K. Rankin,et al. Binge eating is associated with right orbitofrontal-insular-striatal atrophy in frontotemporal dementia , 2007, Neurology.
[64] J. Merrilees. A Model for Management of Behavioral Symptoms in Frontotemporal Lobar Degeneration , 2007, Alzheimer disease and associated disorders.
[65] D. Geschwind,et al. Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative , 2007, The Lancet Neurology.
[66] P. Johannsen,et al. A Reassessment of the Neuropathology of Frontotemporal Dementia Linked to Chromosome 3 , 2007, Journal of neuropathology and experimental neurology.
[67] K Patterson,et al. Focal cortical presentations of Alzheimer's disease. , 2007, Brain : a journal of neurology.
[68] B. Boeve,et al. Frontotemporal Dementia Treatment: Current Symptomatic Therapies and Implications of Recent Genetic, Biochemical, and Neuroimaging Studies , 2007, Alzheimer disease and associated disorders.
[69] C. DeCarli,et al. FDG-PET improves accuracy in distinguishing frontotemporal dementia and Alzheimer's disease. , 2007, Brain : a journal of neurology.
[70] L. Petrucelli,et al. Progranulin Mediates Caspase-Dependent Cleavage of TAR DNA Binding Protein-43 , 2007, The Journal of Neuroscience.
[71] B. Dubois,et al. Progranulin null mutations in both sporadic and familial frontotemporal dementia , 2007, Human mutation.
[72] M. Weiner,et al. Patterns of MRI atrophy in tau positive and ubiquitin positive frontotemporal lobar degeneration , 2007, Journal of Neurology, Neurosurgery, and Psychiatry.
[73] J. Morris,et al. TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions. , 2007, The American journal of pathology.
[74] J. Schneider,et al. Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration , 2007, Acta Neuropathologica.
[75] I. Mackenzie. The neuropathology and clinical phenotype of FTD with progranulin mutations , 2007, Acta Neuropathologica.
[76] J. Trojanowski,et al. Cognitive and motor assessment in autopsy-proven corticobasal degeneration , 2007, Neurology.
[77] B. Miller,et al. 11C-PIB PET imaging in Alzheimer disease and frontotemporal lobar degeneration , 2007, Neurology.
[78] Andrew Kertesz,et al. The Diagnosis and Course of Frontotemporal Dementia , 2007, Alzheimer disease and associated disorders.
[79] M. Swanberg. Memantine for Behavioral Disturbances in Frontotemporal Dementia: A Case Series , 2007, Alzheimer disease and associated disorders.
[80] Clifford R Jack,et al. Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations. , 2007, Archives of neurology.
[81] Murray Grossman,et al. TDP-43-Positive White Matter Pathology in Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions , 2007, Journal of neuropathology and experimental neurology.
[82] D. Dickson,et al. Journal of Neuroinflammation BioMed Central Review , 2006 .
[83] Matthias J. Müller,et al. Clinical improvement in a case of frontotemporal dementia under aripiprazole treatment corresponds to partial recovery of disturbed frontal glucose metabolism , 2007, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.
[84] M. Mendez,et al. Preliminary findings: behavioral worsening on donepezil in patients with frontotemporal dementia. , 2007, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.
[85] C. van Broeckhoven,et al. Progranulin mutations in ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. , 2006, Current Alzheimer research.
[86] B L Miller,et al. Behavioral features in semantic dementia vs other forms of progressive aphasias , 2006, Neurology.
[87] J. Hodges,et al. Progression in frontotemporal dementia: identifying a benign behavioral variant by magnetic resonance imaging. , 2006, Archives of neurology.
[88] D. Neary,et al. Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia. , 2006, Brain : a journal of neurology.
[89] S. Melquist,et al. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. , 2006, Human molecular genetics.
[90] Bruce L. Miller,et al. Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis , 2006, Science.
[91] J. Collinge,et al. ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B) , 2006, Neurology.
[92] P. Pietrini,et al. Characteristics of frontotemporal dementia patients with a Progranulin mutation , 2006, Annals of neurology.
[93] S. Melquist,et al. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 , 2006, Nature.
[94] D. Neary,et al. Dementia lacking distinctive histology (DLDH) revisited , 2006, Acta Neuropathologica.
[95] Jennifer L. Whitwell,et al. Clinicopathological and imaging correlates of progressive aphasia and apraxia of speech. , 2006, Brain : a journal of neurology.
[96] Jennifer Farmer,et al. Frontotemporal dementia: Clinicopathological correlations , 2006, Annals of neurology.
[97] I. Litvan,et al. Current and future treatments in progressive supranuclear palsy , 2006, Current treatment options in neurology.
[98] F. Baas,et al. Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3. , 2006, Brain : a journal of neurology.
[99] H. Horvitz,et al. A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia , 2006, Neurology.
[100] M. Gorno-Tempini,et al. Clinical and neuropsychological features of corticobasal degeneration , 2006, Mechanisms of Ageing and Development.
[101] Joseph James Duffy,et al. Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP , 2006, Neurology.
[102] Jordan Grafman,et al. A systematic review of neurotransmitter deficits and treatments in frontotemporal dementia , 2006, Neurology.
[103] Karalyn Patterson,et al. Clinical and pathological characterization of progressive aphasia , 2006, Annals of neurology.
[104] Maria Luisa Gorno-Tempini,et al. Patterns of brain atrophy that differentiate corticobasal degeneration syndrome from progressive supranuclear palsy. , 2006, Archives of neurology.
[105] S Minoshima,et al. Diagnosis and management of dementia with Lewy bodies , 2005, Neurology.
[106] J. Neuhaus,et al. Comparison of family histories in FTLD subtypes and related tauopathies , 2005, Neurology.
[107] Guido F. Schauer,et al. Neuroanatomical correlates of behavioural disorders in dementia. , 2005, Brain : a journal of neurology.
[108] K Yaffe,et al. Frontotemporal dementia progresses to death faster than Alzheimer disease , 2005, Neurology.
[109] Andrew Kertesz,et al. The evolution and pathology of frontotemporal dementia. , 2005, Brain : a journal of neurology.
[110] Nick C Fox,et al. Magnetic resonance imaging signatures of tissue pathology in frontotemporal dementia. , 2005, Archives of neurology.
[111] C. DeCarli,et al. Rate of progression differs in frontotemporal dementia and Alzheimer disease , 2005, Neurology.
[112] M. Mendez,et al. Acquired Sociopathy and Frontotemporal Dementia , 2005, Dementia and Geriatric Cognitive Disorders.
[113] Holger Hummerich,et al. Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia , 2005, Nature Genetics.
[114] J. Shapira,et al. Stereotypical movements and frontotemporal dementia , 2005, Movement disorders : official journal of the Movement Disorder Society.
[115] B. Miller,et al. Frontotemporal lobar degeneration: demographic characteristics of 353 patients. , 2005, Archives of neurology.
[116] B. L. Miller,et al. The natural history of temporal variant frontotemporal dementia , 2005, Neurology.
[117] B L Miller,et al. Self awareness and personality change in dementia , 2005, Journal of Neurology, Neurosurgery & Psychiatry.
[118] Joel H Kramer,et al. Patterns of Cognitive and Emotional Empathy in Frontotemporal Lobar Degeneration , 2005, Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology.
[119] Linda Clare,et al. The ‘Talking About Memory Coffee Group’: A new model of support for people with early-stage dementia and their families , 2005 .
[120] Daniela Perani,et al. Glucose metabolism and serotonin receptors in the frontotemporal lobe degeneration , 2005, Annals of neurology.
[121] Marina Boccardi,et al. Frontotemporal dementia as a neural system disease , 2005, Neurobiology of Aging.
[122] Maria Luisa Gorno-Tempini,et al. Cognitive and Behavioral Profile in a Case of Right Anterior Temporal Lobe Neurodegeneration , 2004, Cortex.
[123] Maria Luisa Gorno-Tempini,et al. Clinical, Cognitive and Anatomical Evolution from Nonfluent Progressive Aphasia to Corticobasal Syndrome: A Case Report , 2004, Neurocase.
[124] E. Devouche,et al. Confabulation, but not executive dysfunction discriminate AD from frontotemporal dementia , 2004, European journal of neurology.
[125] J. Trojanowski,et al. Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease , 2004, Neurology.
[126] J. Kramer,et al. Neuropsychological and Functional Measures of Severity in Alzheimer Disease, Frontotemporal Dementia, and Semantic Dementia , 2004, Alzheimer disease and associated disorders.
[127] C. Broeckhoven,et al. The role of tau (MAPT) in frontotemporal dementia and related tauopathies , 2004, Human mutation.
[128] E. Bigio,et al. Frontotemporal lobar degeneration with motor neuron disease-type inclusions predominates in 76 cases of frontotemporal degeneration , 2004, Acta Neuropathologica.
[129] M N Rossor,et al. Frontotemporal lobar degeneration and ubiquitin immunohistochemistry , 2004, Neuropathology and applied neurobiology.
[130] A. Moosa,et al. Evidence for an association between the CSF HVA:5-HIAA ratio and aggressiveness in frontotemporal dementia but not in Alzheimer's disease. , 2004 .
[131] D. Mann,et al. Frontotemporal dementia with Pick-type histology associated with Q336R mutation in the tau gene. , 2004, Brain : a journal of neurology.
[132] F. Pasquier,et al. Frontotemporal Dementia: A Randomised, Controlled Trial with Trazodone , 2004, Dementia and Geriatric Cognitive Disorders.
[133] C. Lomen‐Hoerth. Characterization of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia , 2004, Dementia and Geriatric Cognitive Disorders.
[134] A. Pestronk,et al. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein , 2004, Nature Genetics.
[135] B L Miller,et al. Behavioral disorders in the frontal and temporal variants of frontotemporal dementia , 2004, Neurology.
[136] M. Ikeda,et al. Efficacy of Fluvoxamine as a Treatment for Behavioral Symptoms in Frontotemporal Lobar Degeneration Patients , 2004, Dementia and Geriatric Cognitive Disorders.
[137] W. Klunk,et al. Imaging brain amyloid in Alzheimer's disease with Pittsburgh Compound‐B , 2004, Annals of neurology.
[138] M. Weiner,et al. Cognition and anatomy in three variants of primary progressive aphasia , 2004, Annals of neurology.
[139] R. Petersen,et al. The incidence of frontotemporal lobar degeneration in Rochester, Minnesota, 1990 through 1994 , 2004, Neurology.
[140] A. Bava,et al. Rivastigmine in Frontotemporal Dementia , 2004, Drugs & aging.
[141] J. Morrison,et al. Amyotrophic lateral sclerosis/parkinsonism-dementia complex of Guam: quantitative neuropathology, immunohistochemical analysis of neuronal vulnerability, and comparison with related neurodegenerative disorders , 2004, Acta Neuropathologica.
[142] D. Mann,et al. The topographic distribution of brain atrophy in frontal lobe dementia , 2004, Acta Neuropathologica.
[143] B. Sahakian,et al. Paroxetine does not improve symptoms and impairs cognition in frontotemporal dementia: a double-blind randomized controlled trial , 2004, Psychopharmacology.
[144] Howard J. Rosen,et al. Distinctive Neuropsychological Patterns in Frontotemporal Dementia, Semantic Dementia, And Alzheimer Disease , 2003, Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology.
[145] Karalyn Patterson,et al. Left/right asymmetry of atrophy in semantic dementia , 2003, Neurology.
[146] D. Dickson,et al. Ultrastructural neuronal pathology in transgenic mice expressing mutant (P301L) human tau , 2003, Journal of neurocytology.
[147] K. Blennow,et al. CSF markers for incipient Alzheimer's disease , 2003, The Lancet Neurology.
[148] Nick C Fox,et al. Neurofilament inclusion body disease: a new proteinopathy? , 2003, Brain : a journal of neurology.
[149] Philip Scheltens,et al. Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study. , 2003, Brain : a journal of neurology.
[150] Zhiheng He,et al. Progranulin (granulin-epithelin precursor, PC-cell-derived growth factor, acrogranin) mediates tissue repair and tumorigenesis , 2003, Journal of Molecular Medicine.
[151] J. Hodges,et al. Survival in frontotemporal dementia , 2003, Neurology.
[152] M. Mesulam,et al. The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathy , 2003, Acta Neuropathologica.
[153] Bin Zhang,et al. Neurodegeneration and defective neurotransmission in a Caenorhabditis elegans model of tauopathy , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[154] A. Bava,et al. Olanzapine as a treatment of neuropsychiatric disorders of Alzheimer's disease and other dementias: A 24-month follow-up of 68 patients , 2003, American journal of Alzheimer's disease and other dementias.
[155] M. Sjögren,et al. The prevalence of frontal variant frontotemporal dementia and the frontal lobe syndrome in a population based sample of 85 year olds , 2003, Journal of neurology, neurosurgery, and psychiatry.
[156] Norbert Schuff,et al. Cinguloparietal atrophy distinguishes Alzheimer disease from semantic dementia. , 2003, Archives of neurology.
[157] I. McKeith,et al. SIC Task Force appraisal of clinical diagnostic criteria for parkinsonian disorders , 2003, Movement disorders : official journal of the Movement Disorder Society.
[158] Trey Sunderland,et al. Decreased beta-amyloid1-42 and increased tau levels in cerebrospinal fluid of patients with Alzheimer disease. , 2003, JAMA.
[159] B. Miller,et al. Are amyotrophic lateral sclerosis patients cognitively normal? , 2003, Neurology.
[160] Rachelle Doody,et al. Memantine in moderate-to-severe Alzheimer's disease. , 2003, The New England journal of medicine.
[161] J. Hodges,et al. Staging disease severity in pathologically confirmed cases of frontotemporal dementia , 2003, Neurology.
[162] Joel H Kramer,et al. Double dissociation of social functioning in frontotemporal dementia , 2003, Neurology.
[163] C. H. Ong,et al. Progranulin is a mediator of the wound response , 2003, Nature Medicine.
[164] Nick C Fox,et al. Vulnerability to neuroleptic side effects in frontotemporal lobar degeneration , 2003, International journal of geriatric psychiatry.
[165] R. Caselli,et al. Cognitive impairment, frontotemporal dementia, and the motor neuron diseases , 2003, Annals of neurology.
[166] A. Delacourte,et al. The neuropathology and biochemistry of frontotemporal dementia , 2003, Annals of neurology.
[167] A. Bava,et al. Frontotemporal Dementia: Paroxetine as a Possible Treatment of Behavior Symptoms , 2002, European Neurology.
[168] S Gydesen,et al. Chromosome 3 linked frontotemporal dementia (FTD-3) , 2002, Neurology.
[169] P. Lantos,et al. Office of Rare Diseases Neuropathologic Criteria for Corticobasal Degeneration , 2002, Journal of neuropathology and experimental neurology.
[170] Catherine Lomen-Hoerth,et al. The overlap of amyotrophic lateral sclerosis and frontotemporal dementia , 2002, Neurology.
[171] K. Heilman,et al. Relative Frequencies of Alzheimer Disease, Lewy Body, Vascular and Frontotemporal Dementia, and Hippocampal Sclerosis in the State of Florida Brain Bank , 2002, Alzheimer disease and associated disorders.
[172] J R Hodges,et al. Changes in appetite, food preference, and eating habits in frontotemporal dementia and Alzheimer’s disease , 2002, Journal of neurology, neurosurgery, and psychiatry.
[173] J. V. van Swieten,et al. New developments in frontotemporal dementia and parkinsonism linked to chromosome 17 , 2002, Current opinion in neurology.
[174] Murray Grossman,et al. Progressive aphasic syndromes: clinical and theoretical advances , 2002, Current opinion in neurology.
[175] J. Trojanowski,et al. Transgenic Mouse Model of Tauopathies with Glial Pathology and Nervous System Degeneration , 2002, Neuron.
[176] Odette A. Harris,et al. The role of hypothermia in the management of severe brain injury: a meta-analysis. , 2002, Archives of neurology.
[177] L A Hansen,et al. Cognitive profiles differ in autopsy-confirmed frontotemporal dementia and AD , 2002, Neurology.
[178] J R Hodges,et al. The prevalence of frontotemporal dementia , 2002, Neurology.
[179] B L Miller,et al. Utility of clinical criteria in differentiating frontotemporal lobar degeneration (FTLD) from AD , 2002, Neurology.
[180] J. Trojanowski,et al. Sporadic Pick's disease: A tauopathy characterized by a spectrum of pathological τ isoforms in gray and white matter , 2002, Annals of neurology.
[181] M. Laine,et al. Striatal dopamine transporter and extrapyramidal symptoms in frontotemporal dementia , 2002, Neurology.
[182] D. Geschwind,et al. Human Wild-Type Tau Interacts with wingless Pathway Components and Produces Neurofibrillary Pathology in Drosophila , 2002, Neuron.
[183] T. Iwatsubo,et al. Late‐onset frontotemporal dementia with a novel exon 1 (Arg5His) tau gene mutation , 2002, Annals of neurology.
[184] L. Forno,et al. Ubiquitin-positive neuronal and tau 2-positive glial inclusions in frontotemporal dementia of motor neuron type , 2002, Acta Neuropathologica.
[185] B L Miller,et al. Patterns of brain atrophy in frontotemporal dementia and semantic dementia , 2002, Neurology.
[186] Norbert Schuff,et al. Patterns of cerebral atrophy in primary progressive aphasia. , 2002, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.
[187] Masatoshi Suzuki,et al. Granulin precursor gene: a sex steroid-inducible gene involved in sexual differentiation of the rat brain. , 2002, Molecular genetics and metabolism.
[188] James L. McClelland,et al. Deficits in irregular past-tense verb morphology associated with degraded semantic knowledge , 2001, Neuropsychologia.
[189] D. Geschwind,et al. Dementia and neurodevelopmental predisposition: Cognitive dysfunction in presymptomatic subjects precedes dementia by decades in frontotemporal dementia , 2001, Annals of neurology.
[190] Mark A. Levenstien,et al. Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia. , 2001, Molecular genetics and metabolism.
[191] J. Trojanowski,et al. Update on the Neuropathological Diagnosis of Frontotemporal Dementias , 2001, Journal of neuropathology and experimental neurology.
[192] Nick C Fox,et al. Rates of global and regional cerebral atrophy in AD and frontotemporal dementia , 2001, Neurology.
[193] G. Alexander,et al. Positron emission tomography in evaluation of dementia: Regional brain metabolism and long-term outcome. , 2001, JAMA.
[194] 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.
[195] J. Hardy,et al. The genetic and pathological classification of familial frontotemporal dementia. , 2001, Archives of neurology.
[196] R. Crowther,et al. Pick's disease associated with the novel Tau gene mutation K369I , 2001, Annals of neurology.
[197] D. Dickson,et al. Analysis of tauopathies with transgenic mice. , 2001, Trends in molecular medicine.
[198] W. Kamphorst,et al. Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22. , 2001, Brain : a journal of neurology.
[199] J R Hodges,et al. Episodic memory: insights from semantic dementia. , 2001, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[200] K. Boone,et al. Neuroanatomy of the self , 2001, Neurology.
[201] B. Sahakian,et al. Differing patterns of temporal atrophy in Alzheimer’s disease and semantic dementia , 2001, Neurology.
[202] M N Rossor,et al. Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype , 2001, Neurology.
[203] Joshua M. Shulman,et al. Tauopathy in Drosophila: Neurodegeneration Without Neurofibrillary Tangles , 2001, Science.
[204] M. Grossman. A multidisciplinary approach to Pick’s disease and frontotemporal dementia , 2001, Neurology.
[205] I. Litvan. Therapy and management of frontal lobe dementia patients , 2001, Neurology.
[206] D. Dickson. Neuropathology of Pick’s disease , 2001, Neurology.
[207] L. Evans,et al. Responding to safety issues in frontotemporal dementias , 2001, Neurology.
[208] R. J. Perry,et al. Behavior and treatment in frontotemporal dementia , 2001, Neurology.
[209] J. Hodges. Frontotemporal dementia (Pick’s disease): Clinical features and assessment , 2001, Neurology.
[210] M. Hutton. Missense and splice site mutations in tau associated with FTDP-17: Multiple pathogenic mechanisms , 2001, Neurology.
[211] B. L. Miller,et al. The influence of right frontotemporal dysfunction on social behavior in frontotemporal dementia , 2001, Neurology.
[212] M. Mesulam. Primary progressive aphasia , 2001, Annals of neurology.
[213] H. P. Schmitt,et al. Frontotemporal dementia: evidence for impairment of ascending serotoninergic but not noradrenergic innervation , 2001, Acta Neuropathologica.
[214] M N Rossor,et al. Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease , 2001, Annals of neurology.
[215] J. Trojanowski,et al. Loss of brain tau defines novel sporadic and familial tauopathies with frontotemporal dementia , 2001, Annals of neurology.
[216] G. Schellenberg,et al. The case of the missing Tau, or, why didn't the mRNA bark? , 2001, Annals of neurology.
[217] B. Sahakian,et al. Temporal lobe rating scale: application to Alzheimer's disease and frontotemporal dementia , 2001, Journal of neurology, neurosurgery, and psychiatry.
[218] René Hen,et al. Decreased nuclear β‐catenin, tau hyperphosphorylation and neurodegeneration in GSK‐3β conditional transgenic mice , 2001 .
[219] B Miller,et al. The Classification, Genetics and Neuropathology of Frontotemporal Dementia. Introduction to the Special Topic Papers: Part I , 2001, Neurocase.
[220] J R Hodges,et al. Selective impairment of verb processing associated with pathological changes in Brodmann areas 44 and 45 in the motor neurone disease-dementia-aphasia syndrome. , 2001, Brain : a journal of neurology.
[221] I Litvan,et al. The FAB: A frontal assessment battery at bedside , 2000, Neurology.
[222] M. Gaviria,et al. [Fronto-temporal dementia]. , 2000, Actas espanolas de psiquiatria.
[223] A. Kertesz,et al. The corticobasal degeneration syndrome overlaps progressive aphasia and frontotemporal dementia , 2000, Neurology.
[224] D. Neary,et al. Cognitive change in motor neurone disease/amyotrophic lateral sclerosis (MND/ALS) , 2000, Journal of the Neurological Sciences.
[225] J. Hodges,et al. Tau Gene Mutation K257T Causes a Tauopathy Similar to Pick's Disease , 2000, Journal of neuropathology and experimental neurology.
[226] J. Hoffman,et al. FDG PET imaging in patients with pathologically verified dementia. , 2000, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.
[227] J. Haines,et al. Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22. , 2000, JAMA.
[228] Wen-Lang Lin,et al. Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein , 2000, Nature Genetics.
[229] Sasha Bozeat,et al. Which neuropsychiatric and behavioural features distinguish frontal and temporal variants of frontotemporal dementia from Alzheimer's disease? , 2000, Journal of neurology, neurosurgery, and psychiatry.
[230] J. Hodges,et al. Differentiating frontal and temporal variant frontotemporal dementia from Alzheimer’s disease , 2000, Neurology.
[231] R. Curtis,et al. Case of pick's central lobar atrophy with apparent stabilization of cognitive decline after treatment with risperidone. , 2000, Journal of clinical psychopharmacology.
[232] J. Hodges,et al. Semantic dementia: clinical, radiological and pathological perspectives , 2000, Journal of Neurology.
[233] R. A. Crowther,et al. Axonopathy and amyotrophy in mice transgenic for human four-repeat tau protein , 2000, Acta Neuropathologica.
[234] R. D. Williams,et al. Hyperphosphorylated tau and neurofilament and cytoskeletal disruptions in mice overexpressing human p25, an activator of cdk5. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[235] J. Hodges,et al. Insights from semantic dementia on the relationship between episodic and semantic memory , 2000, Neuropsychologia.
[236] M N Rossor,et al. Semantic dementia with ubiquitin-positive tau-negative inclusion bodies. , 2000, Brain : a journal of neurology.
[237] Richard S. J. Frackowiak,et al. A voxel‐based morphometry study of semantic dementia: Relationship between temporal lobe atrophy and semantic memory , 2000, Annals of neurology.
[238] P Nestor,et al. Non-Alzheimer dementias. , 2000, Seminars in neurology.
[239] Bin Zhang,et al. Age-Dependent Emergence and Progression of a Tauopathy in Transgenic Mice Overexpressing the Shortest Human Tau Isoform , 1999, Neuron.
[240] C. Cotman,et al. Clinical and pathological evidence for a frontal variant of Alzheimer disease. , 1999, Archives of neurology.
[241] Bruce L. Miller,et al. Neuroimaging in the Diagnosis of Frontotemporal Dementia , 1999, Dementia and Geriatric Cognitive Disorders.
[242] P. Francis,et al. Neurochemical Features of Frontotemporal Dementia , 1999, Dementia and Geriatric Cognitive Disorders.
[243] D. Geschwind,et al. Inheritance of frontotemporal dementia. , 1999, Archives of neurology.
[244] M G Spillantini,et al. Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau. , 1999, Journal of neuropathology and experimental neurology.
[245] G. Schellenberg,et al. Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[246] J R Hodges,et al. Early diagnosis of the frontal variant of frontotemporal dementia: how sensitive are standard neuroimaging and neuropsychologic tests? , 1999, Neuropsychiatry, neuropsychology, and behavioral neurology.
[247] G. Schellenberg,et al. A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L) , 1999, Brain : a journal of neurology.
[248] I Litvan,et al. Association of an extended haplotype in the tau gene with progressive supranuclear palsy. , 1999, Human molecular genetics.
[249] P. Hof,et al. Phosphorylated serine422 on tau proteins is a pathological epitope found in several diseases with neurofibrillary degeneration , 1999, Acta Neuropathologica.
[250] D. Neary,et al. Evaluation of the NINCDS-ADRDA criteria in the differentiation of Alzheimer’s disease and frontotemporal dementia , 1999, Journal of neurology, neurosurgery, and psychiatry.
[251] C. Price,et al. Disrupted temporal lobe connections in semantic dementia. , 1999 .
[252] G. Schellenberg,et al. Correction: A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L) (Brain (1999) 122, 4 (741-756)) , 1999 .
[253] P Garrard,et al. The differentiation of semantic dementia and frontal lobe dementia (temporal and frontal variants of frontotemporal dementia) from early Alzheimer's disease: a comparative neuropsychological study. , 1999, Neuropsychology.
[254] John X. Morris,et al. Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17. , 1998, Science.
[255] M. Freedman,et al. Frontotemporal lobar degeneration , 1998, Neurology.
[256] J R Hodges,et al. Dementia and aphasia in motor neuron disease: an underrecognised association? , 1998, Journal of neurology, neurosurgery, and psychiatry.
[257] J. Hardy,et al. Genetic classification of primary neurodegenerative disease. , 1998, Science.
[258] M. Goedert,et al. Tau proteins with FTDP‐17 mutations have a reduced ability to promote microtubule assembly , 1998, FEBS letters.
[259] B L Miller,et al. Emergence of artistic talent in frontotemporal dementia , 1998, Neurology.
[260] A Klug,et al. Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[261] Ronald C. Petersen,et al. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 , 1998, Nature.
[262] P. Scheltens,et al. Familial aggregation in frontotemporal dementia , 1998, Neurology.
[263] M. L. Schmidt,et al. Autosomal dominant dementia with widespread neurofibrillary tangles , 1997, Annals of neurology.
[264] D. Benson,et al. Behavioral Phenomenology in Alzheimer's Disease, Frontotemporal Dementia, and Late-Life Depression: A Retrospective Analysis , 1997, Journal of geriatric psychiatry and neurology.
[265] Gerald L. Russell,et al. The temporal variant of frontotemporal dementia. , 1997, Brain : a journal of neurology.
[266] J. Swartz,et al. Frontotemporal dementia: treatment response to serotonin selective reuptake inhibitors. , 1997, The Journal of clinical psychiatry.
[267] K. Boone,et al. A study of the Lund‐Manchester research criteria for frontotemporal dementia , 1997, Neurology.
[268] K. Wilhelmsen. Frontotemporal dementia is on the MAPτ , 1997 .
[269] B. Miller,et al. Aggressive, socially disruptive and antisocial behaviour associated with fronto-temporal dementia , 1997, British Journal of Psychiatry.
[270] J. Lowe,et al. Motor neurone disease-inclusion dementia. , 1996, Neurodegeneration : a journal for neurodegenerative disorders, neuroprotection, and neuroregeneration.
[271] J R Hodges,et al. Nonfluent progressive aphasia and semantic dementia: A comparative neuropsychological study , 1996, Journal of the International Neuropsychological Society.
[272] J. Cummings,et al. Frontotemporal dementia versus Alzheimer's disease , 1996, Neurology.
[273] B L Miller,et al. Alzheimer disease and frontotemporal dementias. Behavioral distinctions. , 1996, Archives of neurology.
[274] M. Hallett,et al. Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) , 1996, Neurology.
[275] J. Hodges,et al. Charting the progression in semantic dementia: implications for the organisation of semantic memory. , 1995, Memory.
[276] J. Grafman,et al. Neuropsychological Features of Progressive Supranuclear Palsy , 1995, Brain and Cognition.
[277] B L Miller,et al. Dietary changes, compulsions and sexual behavior in frontotemporal degeneration. , 1995, Dementia.
[278] John R. Hodges,et al. Progressive prosopagnosia associated with selective right temporal lobe atrophy. A new syndrome? , 1995, Brain : a journal of neurology.
[279] S. Love,et al. Neurofibrillary tangles in Niemann-Pick disease type C. , 1995, Brain : a journal of neurology.
[280] K. Wilhelmsen,et al. Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22. , 1994, American journal of human genetics.
[281] A. Kertesz,et al. The pathology and nosology of primary progressive aphasia , 1994, Neurology.
[282] K. Marder,et al. Clinical characteristics of a family with chromosome 17‐linked disinhibition‐dementia‐ parkinsonism‐amyotrophy complex , 1994, Neurology.
[283] A. Brun,et al. Neuropsychological tests as discriminators between dementia of alzheimer type and frontotemporal dementia , 1994 .
[284] V. Meininger,et al. A controlled trial of riluzole in amyotrophic lateral sclerosis. ALS/Riluzole Study Group. , 1994, The New England journal of medicine.
[285] J. Cummings,et al. Repetitive and compulsive behavior in frontal lobe degenerations. , 1994, The Journal of neuropsychiatry and clinical neurosciences.
[286] D. Neary,et al. Dementia of frontal lobe type: neuropathology and immunohistochemistry. , 1993, Journal of neurology, neurosurgery, and psychiatry.
[287] A. Brun. Frontal lobe degeneration of non-Alzheimer type revisited. , 1993, Dementia.
[288] L. Gustafson,et al. Clinical picture of frontal lobe degeneration of non-Alzheimer type. , 1993, Dementia.
[289] H. Karbe,et al. Profiles of language impairment in primary progressive aphasia. , 1993, Archives of neurology.
[290] M. Mendez,et al. Pick's disease versus Alzheimer's disease , 1993, Neurology.
[291] R. Petersen,et al. Rapidly progressive aphasic dementia and motor neuron disease , 1993, Annals of neurology.
[292] J. Hodges,et al. Dementia of frontal type and the focal lobar atrophies , 1993 .
[293] D. Knopman,et al. Overview of dementia lacking distinctive histology: pathological designation of a progressive dementia. , 1993, Dementia.
[294] J. Hodges,et al. Semantic dementia. Progressive fluent aphasia with temporal lobe atrophy. , 1992, Brain : a journal of neurology.
[295] A. Brun,et al. Frontal lobe degeneration of non‐Alzheimer type , 1992, Bailliere's clinical neurology.
[296] H J Testa,et al. Progressive language disorder due to lobar atrophy , 1992, Annals of neurology.
[297] H. Doshi,et al. Pick's disease , 1991, Neurology.
[298] B. L. Miller,et al. Frontal lobe degeneration , 1991, Neurology.
[299] D. Sparks,et al. Altered serotonergic and cholinergic synaptic markers in Pick's disease. , 1991, Archives of neurology.
[300] M. Mesulam,et al. Primary progressive aphasia. Longitudinal course, neuropsychological profile, and language features. , 1990, Archives of neurology.
[301] D. Benson,et al. Slowly progressive aphasia: three cases with language, memory, CT and PET data. , 1990, Journal of neurology, neurosurgery, and psychiatry.
[302] E. Masliah,et al. Quantitative immunohistochemistry of synaptophysin in human neocortex: an alternative method to estimate density of presynaptic terminals in paraffin sections. , 1990, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.
[303] M. N. Hart,et al. Progressive aphasia in a patient with Pick's disease , 1990, Neurology.
[304] D. Knopman,et al. Dementia lacking distinctive histologie features , 1990, Neurology.
[305] D. Neary,et al. Frontal lobe dementia and motor neuron disease. , 1990, Journal of neurology, neurosurgery, and psychiatry.
[306] D. Neary,et al. Dementia of frontal lobe type. , 1988, Journal of neurology, neurosurgery, and psychiatry.
[307] R. Crowther,et al. Cloning and sequencing of the cDNA encoding an isoform of microtubule‐associated protein tau containing four tandem repeats: differential expression of tau protein mRNAs in human brain. , 1989, The EMBO journal.
[308] D. Neary,et al. Semantic dementia: a form of circumscribed cerebral atrophy , 1995 .
[309] E Capitani,et al. Progressive language impairment without dementia: a case with isolated category specific semantic defect. , 1988, Journal of neurology, neurosurgery, and psychiatry.
[310] R. DeTeresa,et al. Neocortical morphometry and cholinergic neurochemistry in Pick's disease. , 1988, American Journal of Pathology.
[311] C. Luzzatti,et al. Slowly progressive aphasia in three patients. The problem of accompanying neuropsychological deficit. , 1988, Brain : a journal of neurology.
[312] H. Kirshner,et al. Progressive aphasia without dementia: Two cases with focal spongiform degeneration , 1987, Annals of neurology.
[313] A Brun,et al. Frontal lobe degeneration of non-Alzheimer type. I. Neuropathology. , 1987, Archives of gerontology and geriatrics.
[314] L. Gustafson,et al. Frontal lobe degeneration of non-Alzheimer type. II. Clinical picture and differential diagnosis. , 1987, Archives of gerontology and geriatrics.
[315] S. Mirra,et al. FILAMENTOUS AGGREGATES IN PICK'S DISEASE, PROGRESSIVE SUPRANUCLEAR PALSY, AND ALZHEIMER'S DISEASE SHARE ANTIGENIC DETERMINANTS WITH MICROTUBULE-ASSOCIATED PROTEIN, TAU , 1986, The Lancet.
[316] A. Alavi,et al. Slowly progressive aphasia without generalized dementia: Studies with positron emission tomography , 1986, Annals of neurology.
[317] W. Meier-Ruge,et al. Neurochemical enzyme changes in Alzheimer's and Pick's disease. , 1984, Archives of gerontology and geriatrics.
[318] A. Paetau,et al. A post-mortem comparison of the cortical cholinergic system in Alzheimer's disease and Pick's disease , 1983, Journal of the Neurological Sciences.
[319] M. Mesulam,et al. Slowly progressive aphasia without generalized dementia , 1982, Annals of neurology.
[320] J. Simpson,et al. Neurochemical observations in a case of Pick's disease , 1980, Journal of the Neurological Sciences.
[321] E. Warrington. Quarterly Journal of Experimental Psychology the Selective Impairment of Semantic Memory the Selective Impairment of Semantic Memory , 2022 .
[322] J. Constantinidis,et al. Pick’s Disease , 1974 .
[323] E. Richardson,et al. Corticodentatonigral degeneration with neuronal achromasia. , 1968, Archives of neurology.
[324] K. Onari,et al. Anatomische beiträge zur lehre von der pickschen umschriebenen gro\hirnrinden-atrophie („picksche krankheit“) , 1926 .
[325] A. Alzheimer. über eigenartige Krankheitsfälle des späteren Alters , 1911 .
[326] A. Pick. Zur Symptomatologie der linksseitigen Schläfenlappenatrophie. , 1904 .
[327] A. Pick,et al. Uber die Beziehungen der senilen Hirnatrophie zur Aphasie , 1892 .