about
ESDN, a novel neuropilin-like membrane protein cloned from vascular cells with the longest secretory signal sequence among eukaryotes, is up-regulated after vascular injuryAssignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13.Novel missense mutation in charged multivesicular body protein 2B in a patient with frontotemporal dementia.Loss of brain tau defines novel sporadic and familial tauopathies with frontotemporal dementia.Clinical rationale of genetic testing in dementiaGenetics and biology of Alzheimer's disease and frontotemporal lobar degenerationPresenile dementia syndromes: an update on taxonomy and diagnosis.Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17Autophagy in dementias.Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotypeFrontotemporal lobar degeneration: current concepts in the light of recent advances.Frontotemporal lobar degeneration with ubiquitin-positive inclusions: a molecular genetic update.Identification and chromosomal localization of human genes containing CAG/CTG repeats expressed in testis and brain.Epidemiology of early-onset dementia: a review of the literature.A review on primary progressive aphasia.FTD and ALS: a tale of two diseasesNovel types of frontotemporal lobar degeneration: beyond tau and TDP-43.Frontotemporal dementia: from Mendelian genetics towards genome wide association studies.Frontotemporal lobar degeneration: Pathogenesis, pathology and pathways to phenotype.Inheritance of frontotemporal dementia.Frontotemporal dementia genetics.Tau protein in frontotemporal dementia linked to chromosome 3 (FTD-3).Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval.A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21.Frontotemporal dementia linked to chromosome 3 (FTD-3)--current concepts and the detection of a previously unknown branch of the Danish FTD-3 family.Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis.New genes, new dilemmas: FTLD genetics and its implications for families.Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis
P2860
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P2860
description
1995 nî lūn-bûn
@nan
1995 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Familial non-specific dementia maps to chromosome 3
@ast
Familial non-specific dementia maps to chromosome 3
@en
Familial non-specific dementia maps to chromosome 3
@nl
type
label
Familial non-specific dementia maps to chromosome 3
@ast
Familial non-specific dementia maps to chromosome 3
@en
Familial non-specific dementia maps to chromosome 3
@nl
prefLabel
Familial non-specific dementia maps to chromosome 3
@ast
Familial non-specific dementia maps to chromosome 3
@en
Familial non-specific dementia maps to chromosome 3
@nl
P2093
P356
P1476
Familial non-specific dementia maps to chromosome 3
@en
P2093
P304
P356
10.1093/HMG/4.9.1625
P407
P577
1995-09-01T00:00:00Z