Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations.
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Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansionPrimary progressive aphasias and their contribution to the contemporary knowledge about the brain-language relationshipNeuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadicsPhenotypic Heterogeneity of Monogenic Frontotemporal DementiaInvited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimagingFrontotemporal dementia: a bridge between dementia and neuromuscular diseaseTargeted manipulation of the sortilin-progranulin axis rescues progranulin haploinsufficiencyProgranulin is expressed within motor neurons and promotes neuronal cell survivalFrontotemporal lobar degeneration: epidemiology, pathophysiology, diagnosis and management.Syndromes of nonfluent primary progressive aphasia: a clinical and neurolinguistic analysis.Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutationsThe diagnosis of young-onset dementia.Genetic modifiers in carriers of repeat expansions in the C9ORF72 gene.Are there susceptibility factors for primary progressive aphasia?Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family.Predicting functional decline in behavioural variant frontotemporal dementia.An algorithm for genetic testing of frontotemporal lobar degenerationTrajectories of brain and hippocampal atrophy in FTD with mutations in MAPT or GRN.Altered functional connectivity in asymptomatic MAPT subjects: a comparison to bvFTDDistinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutationsClinico-pathological correlations of the most common neurodegenerative dementias.Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.Frontal asymmetry in behavioral variant frontotemporal dementia: clinicoimaging and pathogenetic correlates.No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort.Update on frontotemporal dementia.Progranulin: an emerging target for FTLD therapies.Novel progranulin mutation detected in 2 patients with FTLD.Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRNTDP-43 is a culprit in human neurodegeneration, and not just an innocent bystander.Update on recent molecular and genetic advances in frontotemporal lobar degeneration.FTD and ALS: a tale of two diseasesThe syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis.Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort.Distinct anatomical subtypes of the behavioural variant of frontotemporal dementia: a cluster analysis study.Two distinct subtypes of right temporal variant frontotemporal dementia.The heritability and genetics of frontotemporal lobar degeneration.The molecular basis of frontotemporal dementia.Early-onset dementias: diagnostic and etiological considerations.Progranulin-associated PiB-negative logopenic primary progressive aphasia.Primary progressive aphasia: clinicopathological correlations.
P2860
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P2860
Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Frequency and clinical charact ...... h MAPT and no known mutations.
@en
type
label
Frequency and clinical charact ...... h MAPT and no known mutations.
@en
prefLabel
Frequency and clinical charact ...... h MAPT and no known mutations.
@en
P2093
P2860
P356
P1433
P1476
Frequency and clinical charact ...... h MAPT and no known mutations.
@en
P2093
Anna M T Richardson
Anoop Varma
Daniel Du Plessis
David M A Mann
David Neary
Karen E Morrison
Sara Rollinson
P2860
P304
P356
10.1093/BRAIN/AWM331
P407
P577
2008-01-11T00:00:00Z