Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes
about
An update on semantic dementia: genetics, imaging, and pathologyFrontotemporal Dementia.Opening up the DNA methylome of dementiaAtypical Parkinsonian syndromes: a general neurologist's perspective.Disrupted Face Processing in Frontotemporal Dementia: A Review of the Clinical and Neuroanatomical Evidence.Frontotemporal lobar degeneration: Pathogenesis, pathology and pathways to phenotype.Advances in progressive supranuclear palsy: new diagnostic criteria, biomarkers, and therapeutic approaches.Imaging and fluid biomarkers in frontotemporal dementia.Which ante mortem clinical features predict progressive supranuclear palsy pathology?Hippocampal Sclerosis in Older Patients: Practical Examples and Guidance With a Focus on Cerebral Age-Related TDP-43 With Sclerosis.Overlapping but distinct TDP-43 and tau pathologic patterns in aged hippocampi.A clinicopathological approach to the diagnosis of dementia.Brain gray matter abnormalities in progressive supranuclear palsy revisited.The Amygdala as a Locus of Pathologic Misfolding in Neurodegenerative Diseases.Primary progressive aphasia: a clinical approach.Neurotransmitter deficits from frontotemporal lobar degeneration.Distribution of Types of Dementia in the First 100 Patients Seen at a Dementia Clinic in India.Aphasia in Progressive Supranuclear Palsy: As Severe as Progressive Non-Fluent Aphasia.Mendelian forms of disease and age at onset affect survival in frontotemporal dementia.Intrafamilial variable phenotype including corticobasal syndrome in a family with p.P301L mutation in the MAPT gene: first report in South America.Ageing as a risk factor for ALS/FTD.White matter change with apathy and impulsivity in frontotemporal lobar degeneration syndromes.Corticobasal degeneration: key emerging issues.Neuroimmune Tau Mechanisms: Their Role in the Progression of Neuronal Degeneration.Progress and Challenges in Frontotemporal Dementia Research: A 20-Year Review.Social Cognition Dysfunctions in Neurodegenerative Diseases: Neuroanatomical Correlates and Clinical Implications.Determining the incidence of familiality in ALS: A study of temporal trends in Ireland from 1994 to 2016.Clinical Studies of Social Neuroscience: A Lesion Model ApproachClinical, Anatomical, and Pathological Features in the Three Variants of Primary Progressive Aphasia: A ReviewPrimary progressive aphasia: a review of neuropsychological tests for the assessment of speech and language disordersDivergent brain gene expression patterns associate with distinct cell-specific tau neuropathology traits in progressive supranuclear palsyIntrafamilial Phenotypic Variability in the Gene Expansion: 2 Case Studies
P2860
Q28069807-2F65E608-A2A2-4454-A63E-9F5CF8DB9EDCQ30234793-30E2A64A-0AF2-4F0E-9978-9DBC3755AA71Q37736146-BAC22652-CA60-4FD5-AEFC-635FA9C952DAQ38372272-715D4C48-B6D6-488E-B4E6-B39D5174E111Q38381873-6B30625D-FCA9-41F4-BBEB-0CD7324E890CQ38382217-6F1C382F-9819-46FF-87CE-3109566D7836Q38666247-6A855D8F-2907-449A-96EB-1931A17AFF6AQ38670219-ECC6E752-4B74-4888-9011-A173D1473D6BQ38788274-7C228AE3-644A-4B6E-ADDA-83AFB8D46583Q38807207-45E6F88D-55C3-46A8-93D6-894B94FD7A5DQ38915426-6707C634-C461-4191-82F1-4402406188C1Q39434968-FCB0B997-8B59-4372-BDFE-593C5ED454FEQ45928844-CB744854-B069-4633-AC90-85707118B589Q46251905-E6C77B0A-F2E3-4CB8-BCD7-FF76B4694A2DQ47697896-365B7CF2-59DD-4A57-9461-976FB2C38ABAQ47837913-1C5728C4-4A6E-4CCC-BCAE-06BDF6AE726CQ47838450-B76FC9F3-0CD9-4009-A91E-184768F30C5CQ47908335-ECD44581-665E-4114-B22F-0A8F57BF2F63Q47908840-B7880A2F-CE46-4906-A0E5-D549FF8914C6Q47952791-8809E77D-72AC-4DC1-B0B9-A359B01E2918Q49608524-644D0AE0-21CC-4481-AD86-884201263E5FQ49914494-8105D62D-FDA8-42C3-A294-46A1CBEA2AB1Q50074075-51CF760C-E859-450F-92E6-CBE5BD838654Q52344625-79C5CBB9-AEEC-4C6C-923E-7FCBFE35DE9AQ53441607-552F4977-0345-41A6-AE6A-24C740991849Q55094741-76540EFD-F3A5-43B1-9006-ABEE227E5DCFQ55378327-05CEDD8C-BF03-46D3-B295-64283A1B0C5FQ56787135-26A7BFF7-D10B-4DEF-946E-F18597D6CAD5Q57168245-29617D6B-89FC-4449-AF5C-59FF5E44A30FQ58249656-D8D51CEE-173A-4C7C-9E8D-EEE22644380DQ58716431-44881B3B-5701-4548-AD22-9691794781B2Q58767380-8C846A7B-5AFD-44AA-BE52-F8B389242772
P2860
Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes
@en
type
label
Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes
@en
prefLabel
Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes
@en
P2093
P2860
P50
P1433
P1476
Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes
@en
P2093
Alicia Wilcox
Claire J Lansdall
Eileen Wehmann
Julie Wiggins
Karalyn Patterson
Kate E Dawson
Katrina M Dick
Patricia Vázquez Rodríquez
Simon Mead
P2860
P304
P356
10.1212/WNL.0000000000002638
P407
P577
2016-04-01T00:00:00Z