Frontotemporal Lobar Degeneration

Keith A. Josephs

doi:10.1016/j.ncl.2007.03.005

Frontotemporal Lobar Degeneration

Keith A. Josephs

Neurology

Research output: Contribution to journal › Review article › peer-review

21 Scopus citations

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 language	English (US)
Pages (from-to)	683-696
Number of pages	14
Journal	Neurologic clinics
Volume	25
Issue number	3
DOIs	https://doi.org/10.1016/j.ncl.2007.03.005
State	Published - Aug 2007

ASJC Scopus subject areas

Clinical Neurology

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10.1016/j.ncl.2007.03.005

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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 A.}",

year = "2007",

month = aug,

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",

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TY - JOUR

T1 - Frontotemporal Lobar Degeneration

AU - Josephs, Keith A.

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.

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DO - 10.1016/j.ncl.2007.03.005

M3 - Review article

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AN - SCOPUS:34447301517

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SP - 683

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JO - Neurologic Clinics

JF - Neurologic Clinics

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Frontotemporal Lobar Degeneration

Abstract

ASJC Scopus subject areas

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