Frontotemporal demens heterogen sjukdomsgrupp.

Research output: Contribution to journalArticle

Standard

Frontotemporal demens heterogen sjukdomsgrupp. / Landqvist, Maria; Elfgren, Christina; Englund, Elsabet; Nilsson, Christer; Passant, Ulla.

In: Läkartidningen, Vol. 106, No. 20, 2009, p. 1381-1385.

Research output: Contribution to journalArticle

Harvard

Landqvist, M, Elfgren, C, Englund, E, Nilsson, C & Passant, U 2009, 'Frontotemporal demens heterogen sjukdomsgrupp.', Läkartidningen, vol. 106, no. 20, pp. 1381-1385.

APA

Landqvist, M., Elfgren, C., Englund, E., Nilsson, C., & Passant, U. (2009). Frontotemporal demens heterogen sjukdomsgrupp. Läkartidningen, 106(20), 1381-1385.

CBE

Landqvist M, Elfgren C, Englund E, Nilsson C, Passant U. 2009. Frontotemporal demens heterogen sjukdomsgrupp. Läkartidningen. 106(20):1381-1385.

MLA

Vancouver

Landqvist M, Elfgren C, Englund E, Nilsson C, Passant U. Frontotemporal demens heterogen sjukdomsgrupp. Läkartidningen. 2009;106(20):1381-1385.

Author

Landqvist, Maria ; Elfgren, Christina ; Englund, Elsabet ; Nilsson, Christer ; Passant, Ulla. / Frontotemporal demens heterogen sjukdomsgrupp. In: Läkartidningen. 2009 ; Vol. 106, No. 20. pp. 1381-1385.

RIS

TY - JOUR

T1 - Frontotemporal demens heterogen sjukdomsgrupp.

AU - Landqvist, Maria

AU - Elfgren, Christina

AU - Englund, Elsabet

AU - Nilsson, Christer

AU - Passant, Ulla

N1 - The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Department of Psychogeriatrics (013304000), Department of Psychology (012010000)

PY - 2009

Y1 - 2009

N2 - Frontotemporal lobar degeneration (FTLD) or frontotemporal dementia (FTD) is a clinically and neuropathologically heterogeneous group of primary degenerative dementia diseases. The clinical representation consists of progressive psychiatric and/or neurological symtoms such as behavioural changes, language or motor dysfunction. FTD is usually divided into the following subgroups: Behavioural variant FTD (FTD-bv), semantic dementia (SD), progressive non-fluent aphasia (PNFA) and FTD with motor neuron disease (FTD-MND). Progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD) show both clinical and neuropathological similarities to FTD, and therefore are often considered being part of the FTD complex. Knowledge about the great diversity in phenotype of FTD facilitates early refererral and diagnosis of patients, which is necessary for adequate support and treatment.

AB - Frontotemporal lobar degeneration (FTLD) or frontotemporal dementia (FTD) is a clinically and neuropathologically heterogeneous group of primary degenerative dementia diseases. The clinical representation consists of progressive psychiatric and/or neurological symtoms such as behavioural changes, language or motor dysfunction. FTD is usually divided into the following subgroups: Behavioural variant FTD (FTD-bv), semantic dementia (SD), progressive non-fluent aphasia (PNFA) and FTD with motor neuron disease (FTD-MND). Progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD) show both clinical and neuropathological similarities to FTD, and therefore are often considered being part of the FTD complex. Knowledge about the great diversity in phenotype of FTD facilitates early refererral and diagnosis of patients, which is necessary for adequate support and treatment.

KW - Dementia: classification

KW - Brain: pathology

KW - Dementia: genetics

KW - Dementia: diagnosis

KW - Dementia: pathology

M3 - Artikel i vetenskaplig tidskrift

VL - 106

SP - 1381

EP - 1385

JO - Läkartidningen

T2 - Läkartidningen

JF - Läkartidningen

SN - 0023-7205

IS - 20

ER -