Development and validation of pedigree classification criteria for frontotemporal lobar degeneration. - Wikidata - wikimedia - TriplyDB

Development and validation of pedigree classification criteria for frontotemporal lobar degeneration.

Development and validation of pedigree classification criteria for frontotemporal lobar degeneration.

http://www.wikidata.org/entity/Q37531130

about

Myelin oligodendrocyte basic protein and prognosis in behavioral-variant frontotemporal dementia.ALS-Plus syndrome: non-pyramidal features in a large ALS cohort.Frontotemporal lobar degeneration: defining phenotypic diversity through personalized medicine.C9orf72 promoter hypermethylation is neuroprotective: Neuroimaging and neuropathologic evidence.Semi-automated quantification of C9orf72 expansion size reveals inverse correlation between hexanucleotide repeat number and disease duration in frontotemporal degeneration Genetic and neuroanatomic associations in sporadic frontotemporal lobar degeneration.The C9ORF72 expansion mutation: gene structure, phenotypic and diagnostic issues.Biomarkers in the primary progressive aphasias Clinical marker for Alzheimer disease pathology in logopenic primary progressive aphasia.Neurodegeneration and sport.Genetics of FTLD: overview and what else we can expect from genetic studies.Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria.What we know about TMEM106B in neurodegeneration.Predictive genetic testing for amyotrophic lateral sclerosis and frontotemporal dementia: genetic counselling considerations.Neuron loss and degeneration in the progression of TDP-43 in frontotemporal lobar degeneration.Ante mortem cerebrospinal fluid tau levels correlate with postmortem tau pathology in frontotemporal lobar degeneration.Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol.Multimodal imaging evidence of pathology-mediated disease distribution in corticobasal syndrome.The Heritability of Frontotemporal Lobar Degeneration: Validation of Pedigree Classification Criteria in a Northern Italy Cohort.Optical coherence tomography identifies outer retina thinning in frontotemporal degeneration.Expansion of the classification of FTLD-TDP: distinct pathology associated with rapidly progressive frontotemporal degeneration.Progranulin-mediated deficiency of cathepsin D results in FTD and NCL-like phenotypes in neurons derived from FTD patients.A 2-Step Cerebrospinal Algorithm for the Selection of Frontotemporal Lobar Degeneration Subtypes.Progress and Challenges in Frontotemporal Dementia Research: A 20-Year Review.Heritability in frontotemporal dementia: more missing pieces?Perfusion alterations converge with patterns of pathological spread in transactive response DNA-binding protein 43 proteinopathies.Loss of Tmem106b is unable to ameliorate frontotemporal dementia-like phenotypes in an AAV mouse model of C9ORF72-repeat induced toxicity.Longitudinal structural gray matter and white matter MRI changes in presymptomatic progranulin mutation carriers.Intrafamilial Phenotypic Variability in the Gene Expansion: 2 Case Studies

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Development and validation of pedigree classification criteria for frontotemporal lobar degeneration.

http://www.wikidata.org/entity/Q37531130

description

2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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Development and validation of ...... totemporal lobar degeneration.

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Development and validation of ...... totemporal lobar degeneration.

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Development and validation of ...... totemporal lobar degeneration.

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Development and validation of ...... totemporal lobar degeneration.

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Development and validation of ...... totemporal lobar degeneration.

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Development and validation of ...... totemporal lobar degeneration.

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Development and validation of ...... totemporal lobar degeneration.

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Alice S Chen-Plotkin

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Dana Falcone

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David J Irwin

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Edward B Lee

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Elisabeth M Wood

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Eunran Suh

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Sharon X Xie

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Vivianna M Van Deerlin

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P2860

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

Classification of primary progressive aphasia and its variants

Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

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

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

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

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

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

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1411-1417

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10.1001/JAMANEUROL.2013.3956

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Murray Grossman

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