An algorithm for genetic testing of frontotemporal lobar degeneration
about
Parkinsonian syndrome in familial frontotemporal dementiaDiagnosis and management of behavioral variant frontotemporal dementiaThe genetics of dementia.The non-fluent/agrammatic variant of primary progressive aphasia.New approaches to genetic counseling and testing for Alzheimer's disease and frontotemporal degenerationMissense mutations in progranulin gene associated with frontotemporal lobar degeneration: study of pathogenetic featuresCase records of the Massachusetts General Hospital. Case 9-2015. A 31-year-old man with personality changes and progressive neurologic decline.A review of quality of life after predictive testing for and earlier identification of neurodegenerative diseases.Multimodal comparative studies of neurodegenerative diseases.Frontotemporal degeneration, the next therapeutic frontier: molecules and animal models for frontotemporal degeneration drug development.Treatment implications of C9ORF72."Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide.Clinical Subtypes of Frontotemporal Dementia.Atypical association of semantic dementia, corticobasal syndrome, and 4R tauopathy.Neuroimaging and biochemical markers in the three variants of primary progressive aphasia.Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol.Parkinsonism and frontotemporal dementia: the clinical overlap.The patterns of inheritance in early-onset dementia: Alzheimer's disease and frontotemporal dementia.EFNS-ENS Guidelines on the diagnosis and management of disorders associated with dementia.Aprosodic speech with insular hyperintensities and 4R Tau pathology on autopsy.Frontotemporal Dementia Caused by the P301L Mutation in the MAPT Gene: Clinicopathological Features of 13 Cases from the Same Geographical Origin in Barcelona, Spain.C9ORF72 G4C2-repeat expansion and frontotemporal dementia first reported case in Argentina.Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: a multicenter Italian study.Frontotemporal dementia.
P2860
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P2860
An algorithm for genetic testing of frontotemporal lobar degeneration
description
2011 nî lūn-bûn
@nan
2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
An algorithm for genetic testing of frontotemporal lobar degeneration
@ast
An algorithm for genetic testing of frontotemporal lobar degeneration
@en
An algorithm for genetic testing of frontotemporal lobar degeneration
@nl
type
label
An algorithm for genetic testing of frontotemporal lobar degeneration
@ast
An algorithm for genetic testing of frontotemporal lobar degeneration
@en
An algorithm for genetic testing of frontotemporal lobar degeneration
@nl
prefLabel
An algorithm for genetic testing of frontotemporal lobar degeneration
@ast
An algorithm for genetic testing of frontotemporal lobar degeneration
@en
An algorithm for genetic testing of frontotemporal lobar degeneration
@nl
P2093
P2860
P1433
P1476
An algorithm for genetic testing of frontotemporal lobar degeneration
@en
P2093
B L Miller
J S Goldman
R Rademakers
P2860
P304
P356
10.1212/WNL.0B013E31820A0D13
P407
P577
2011-02-01T00:00:00Z