Frontotemporal Lobar Degeneration

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Frontotemporal lobar degeneration (FTLD) is a syndromic diagnosis that encompasses at least three different variants. Imaging modalities are clinically useful in FTLD, although pathology remains the gold standard for definitive diagnosis. To date, four different genes have been identified that account for FTLD.

Original languageEnglish (US)
Pages (from-to)683-696
Number of pages14
JournalNeurologic Clinics
Volume25
Issue number3
DOIs
StatePublished - Aug 2007

Fingerprint

Frontotemporal Lobar Degeneration
Pathology
Genes

ASJC Scopus subject areas

  • Clinical Neurology

Cite this

Frontotemporal Lobar Degeneration. / Josephs, Keith Anthony.

In: Neurologic Clinics, Vol. 25, No. 3, 08.2007, p. 683-696.

Research output: Contribution to journalArticle

@article{9d5c9afc8b904b4899808f7293a71325,
title = "Frontotemporal Lobar Degeneration",
abstract = "Frontotemporal lobar degeneration (FTLD) is a syndromic diagnosis that encompasses at least three different variants. Imaging modalities are clinically useful in FTLD, although pathology remains the gold standard for definitive diagnosis. To date, four different genes have been identified that account for FTLD.",
author = "Josephs, {Keith Anthony}",
year = "2007",
month = "8",
doi = "10.1016/j.ncl.2007.03.005",
language = "English (US)",
volume = "25",
pages = "683--696",
journal = "Neurologic Clinics",
issn = "0733-8619",
publisher = "W.B. Saunders Ltd",
number = "3",

}

TY - JOUR

T1 - Frontotemporal Lobar Degeneration

AU - Josephs, Keith Anthony

PY - 2007/8

Y1 - 2007/8

N2 - Frontotemporal lobar degeneration (FTLD) is a syndromic diagnosis that encompasses at least three different variants. Imaging modalities are clinically useful in FTLD, although pathology remains the gold standard for definitive diagnosis. To date, four different genes have been identified that account for FTLD.

AB - Frontotemporal lobar degeneration (FTLD) is a syndromic diagnosis that encompasses at least three different variants. Imaging modalities are clinically useful in FTLD, although pathology remains the gold standard for definitive diagnosis. To date, four different genes have been identified that account for FTLD.

UR - http://www.scopus.com/inward/record.url?scp=34447301517&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=34447301517&partnerID=8YFLogxK

U2 - 10.1016/j.ncl.2007.03.005

DO - 10.1016/j.ncl.2007.03.005

M3 - Article

C2 - 17659185

AN - SCOPUS:34447301517

VL - 25

SP - 683

EP - 696

JO - Neurologic Clinics

JF - Neurologic Clinics

SN - 0733-8619

IS - 3

ER -