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Article

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

JAMA neurology - 1 Nov 2013

Wood Elisabeth M, Falcone Dana, Suh Eunran, Irwin David J, Chen-Plotkin Alice S, Lee Edward B, Xie Sharon X, Van Deerlin Vivianna M, Grossman Murray

Abstract excerpt

IMPORTANCE: A significant portion of frontotemporal lobar degeneration (FTLD) is due to inherited gene mutations, and we are unaware of a large sequential series that includes a recently discovered inherited cause of FTLD. There is also great need to develop clinical tools and approaches that will assist clinicians in the identification and counseling of patients with FTLD and their families regarding the...

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Identifiers

PMID: 24081456
DOI: 10.1001/jamaneurol.2013.3956
PMCID: PMC3906581

Genes

GRN
MAPT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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