Leader
|
|
|
00000nz a2200037n 45 0 |
001
|
|
|
WKP|Q114336700
(VIAF cluster)
(Authority/Source Record)
|
003
|
|
|
WKP |
005
|
|
|
20241221010639.0 |
008
|
|
|
241221nneanz||abbn n and d |
035
|
|
|
‡a
(WKP)Q114336700
|
035
|
|
|
‡a
(OCoLC)Q114336700
|
100
|
0 |
|
‡a
Maura Gallo
‡c
researcher
‡9
en
|
670
|
|
|
‡a
Author's Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration.
|
670
|
|
|
‡a
Author's Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
|
670
|
|
|
‡a
Author's C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts
|
670
|
|
|
‡a
Author's Frontotemporal dementia and its subtypes: a genome-wide association study
|
670
|
|
|
‡a
Author's Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
|
670
|
|
|
‡a
Author's Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.
|
670
|
|
|
‡a
Author's Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
|
912
|
|
|
‡a
frontotemporaldementiaanditssubtypesagenomewideassociationstudy
‡A
Frontotemporal dementia and its subtypes: a genome-wide association study
‡9
1
|
912
|
|
|
‡a
geneticmetaanalysisofdiagnosedalzheimersdiseaseidentifiesnewrisklociandimplicatesaβtauimmunityandlipidprocessing
‡A
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
‡9
1
|
912
|
|
|
‡a
potentialgeneticmodifiersofdiseaseriskandageatonsetinpatientswithfrontotemporallobardegenerationandgrnmutationsagenomewideassociationstudy
‡A
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.
‡9
1
|
912
|
|
|
‡a
rarecodingvariantsinplcg2abi3andtrem2implicatemicroglialmediatedinnateimmunityinalzheimersdisease
‡A
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
‡9
1
|
912
|
|
|
‡a
authorcorrectiongeneticmetaanalysisofdiagnosedalzheimersdiseaseidentifiesnewrisklociandimplicatesaβtauimmunityandlipidprocessing
‡A
Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
‡9
1
|
912
|
|
|
‡a
c9orf72aaoandancestryhelpdiscriminatingbehaviouralfromlanguagevariantsinftldcohorts
‡A
C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts
‡9
1
|
919
|
|
|
‡a
associationofthevariantcys139argatgrngenetotheclinicalspectrumoffrontotemporallobardegeneration
‡A
Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration.
‡9
1
|
996
|
|
|
‡2
BNE|XX1780456
|
996
|
|
|
‡2
SUDOC|028682793
|
996
|
|
|
‡2
BAV|495_216017
|
996
|
|
|
‡2
NTA|36417319X
|
996
|
|
|
‡2
BNF|12046819
|
996
|
|
|
‡2
ISNI|0000000000683148
|
997
|
|
|
‡a
0 0 lived 0 0
‡9
1
|