Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs. - Test2 - elhamkhani - TriplyDB

Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs.

Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs.

http://www.wikidata.org/entity/Q34396046

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Phenotypic Heterogeneity of Monogenic Frontotemporal Dementia Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging Tau physiology and pathomechanisms in frontotemporal lobar degeneration TDP-43 as a possible biomarker for frontotemporal lobar degeneration: a systematic review of existing antibodies ALS/FTD Mutation-Induced Phase Transition of FUS Liquid Droplets and Reversible Hydrogels into Irreversible Hydrogels Impairs RNP Granule Function.Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.Genetics of Frontotemporal Dementia.Extra-motor abnormalities in amyotrophic lateral sclerosis: another layer of heterogeneity.Frontotemporal lobar degeneration due to P301L tau mutation showing apathy and severe frontal atrophy but lacking other behavioral changes: A case report and literature review.The roles of intrinsic disorder-based liquid-liquid phase transitions in the "Dr. Jekyll-Mr. Hyde" behavior of proteins involved in amyotrophic lateral sclerosis and frontotemporal lobar degeneration.

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Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs.

http://www.wikidata.org/entity/Q34396046

description

2014 nî lūn-bûn

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2014 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հունվարին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs.

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Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs.

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Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs.

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type

label

Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs.

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Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs.

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Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs.

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Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs.

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Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs.

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Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs.

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NRNEUROL.2013.270

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Nature Reviews Neurology

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Dementia in 2013: frontotemporal lobar degeneration-building on breakthroughs.

@en

P2860

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS.

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.

Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration.

Current insights into the C9orf72 repeat expansion diseases of the FTLD/ALS spectrum.

Dipeptide repeat protein pathology in C9ORF72 mutation cases: clinico-pathological correlations.

Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort.

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study.

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nrneurol.2013.270

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Christine Van Broeckhoven

Julie van der Zee

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2014-01-07T00:00:00Z

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