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Article

TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD

6 Jun 2008

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 18536926
DOI: 10.1007/s00401-008-0395-x

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Related research

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TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLDPMID 18536926Read ↗

Reappraisal of TDP-43 pathology in FTLD-U subtypesSemantic proximity Read ↗

Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome SequencingSemantic proximity Read ↗

TDP-43: an emerging new player in neurodegenerative diseasesSemantic proximity Read ↗

Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing.Semantic proximity Read ↗

TDP-43 functions and pathogenic mechanisms implicated in TDP-43 proteinopathiesSemantic proximity Read ↗

TDP-43: a novel neurodegenerative proteinopathySemantic proximity Read ↗

Expansion of the classification of FTLD-TDP: distinct pathology associated with rapidly progressive frontotemporal degeneration.Semantic proximity Read ↗

Genetic architecture of FTLD-TDP pathological subtypes.Semantic proximity Read ↗

Biomarkers for diseases with TDP-43 pathologySemantic proximity Read ↗

TDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron diseaseSemantic proximity Read ↗

Clinical aspects of TDP-43 proteinopathy, neurofilament inclusion body disease and dementias lacking distinctive proteinopathy.Semantic proximity Read ↗

Genotype-phenotype links in frontotemporal lobar degeneration.Semantic proximity Read ↗

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