Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family. - Wikidata - awgldk - TriplyDB

Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family.

Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family.

http://www.wikidata.org/entity/Q34472281

about

Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion C9ORF72, the new gene on the block, causes C9FTD/ALS: new insights provided by neuropathology The genetics and neuropathology of frontotemporal lobar degeneration Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72 Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD A comprehensive review of amyotrophic lateral sclerosis Phenotypic Heterogeneity of Monogenic Frontotemporal Dementia Cognitive and behavioral features of c9FTD/ALS Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis.Frontotemporal dementia: a bridge between dementia and neuromuscular disease Modeling key pathological features of frontotemporal dementia with C9ORF72 repeat expansion in iPSC-derived human neurons Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansions.Recent advances in the imaging of frontotemporal dementia.Neuropathology of Amyotrophic Lateral Sclerosis and Its Variants.Cerebrospinal fluid neurofilament concentration reflects disease severity in frontotemporal degeneration.Frontotemporal dementia with psychosis, parkinsonism, visuo-spatial dysfunction, upper motor neuron involvement associated to expansion of C9ORF72: a peculiar phenotype?The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS.Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion Grey and white matter changes across the amyotrophic lateral sclerosis-frontotemporal dementia continuum.Brain distribution of dipeptide repeat proteins in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72 An algorithm for genetic testing of frontotemporal lobar degeneration TDP-43 variants of frontotemporal lobar degeneration.The Spectrum of C9orf72-mediated Neurodegeneration and Amyotrophic Lateral Sclerosis.TMEM106B a novel risk factor for frontotemporal lobar degeneration C9orf72 promoter hypermethylation is neuroprotective: Neuroimaging and neuropathologic evidence.Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72 Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.Chromosome 9 ALS and FTD locus is probably derived from a single founder Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion in C9ORF72: clinicopathologic correlation

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Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family.

http://www.wikidata.org/entity/Q34472281

description

2010 nî lūn-bûn

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2010 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Clinical, neuroimaging and neu ...... some 9p-linked FTD-ALS family.

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Clinical, neuroimaging and neu ...... some 9p-linked FTD-ALS family.

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Clinical, neuroimaging and neu ...... some 9p-linked FTD-ALS family.

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type

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Clinical, neuroimaging and neu ...... some 9p-linked FTD-ALS family.

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Clinical, neuroimaging and neu ...... some 9p-linked FTD-ALS family.

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Clinical, neuroimaging and neu ...... some 9p-linked FTD-ALS family.

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prefLabel

Clinical, neuroimaging and neu ...... some 9p-linked FTD-ALS family.

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Clinical, neuroimaging and neu ...... some 9p-linked FTD-ALS family.

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Clinical, neuroimaging and neu ...... some 9p-linked FTD-ALS family.

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JNNP.2009.204081

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Journal of Neurology, Neurosurgery and Psychiatry

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Clinical, neuroimaging and neu ...... some 9p-linked FTD-ALS family.

@en

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Aleksandra Wojtas

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Anna Karydas

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Bradley F Boeve

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Dean Foti

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Eric McDade

http://www.w3.org/2001/XMLSchema#string

Ging-Yuek R Hsiung

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Howard Feldman

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Ian R Mackenzie

http://www.w3.org/2001/XMLSchema#string

Jacob Mirsky

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Jennifer Molano

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P2860

Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD

11C PiB and structural MRI provide complementary information in imaging of Alzheimer's disease and amnestic mild cognitive impairment

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

Comparison of family histories in FTLD subtypes and related tauopathies

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

The Clinical Dementia Rating (CDR): current version and scoring rules

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.

Survival in frontotemporal dementia.

VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder.

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196-203

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scholarly article

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10.1136/JNNP.2009.204081

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2

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82

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Rosa Rademakers

Bruce L. Miller

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2010-06-20T00:00:00Z

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44687081

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20562461

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amyotrophic lateral sclerosis

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3017222

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