Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is increasingly recognized to be a multisystem disorder which includes both clinical and neuropathological features of a frontotemporal lobar degeneration (FTLD). In order to provide a common framework within which to discuss the characteristics of the cognitive a...
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Veröffentlicht in: | Amyotrophic lateral sclerosis 2009-01, Vol.10 (3), p.131-146 |
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creator | Strong, Michael J. Grace, Gloria M. Freedman, Morris Lomen-Hoerth, Cathy Woolley, Susan Goldstein, Laura H. Murphy, Jennifer Shoesmith, Christen Rosenfeld, Jeffery Leigh, P. Nigel Bruijn, Lucie Ince, Paul Figlewicz, Denise |
description | Amyotrophic lateral sclerosis (ALS) is increasingly recognized to be a multisystem disorder which includes both clinical and neuropathological features of a frontotemporal lobar degeneration (FTLD). In order to provide a common framework within which to discuss the characteristics of the cognitive and behavioural syndromes of ALS, and with which to conduct clinical and neuropathological research, an international research workshop on frontotemporal dementia (FTD) and ALS was held in London, Canada in June 2007. The recommendations arising from this research workshop address the requirement for a concise clinical diagnosis of the underlying motor neuron disease (Axis I), defining the cognitive and behavioural dysfunction (Axis II), describing additional non-motor manifestations (Axis III) and identifying the presence of disease modifiers (Axis IV). |
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Nigel</creatorcontrib><creatorcontrib>Bruijn, Lucie</creatorcontrib><creatorcontrib>Ince, Paul</creatorcontrib><creatorcontrib>Figlewicz, Denise</creatorcontrib><title>Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis</title><title>Amyotrophic lateral sclerosis</title><addtitle>Amyotroph Lateral Scler</addtitle><description>Amyotrophic lateral sclerosis (ALS) is increasingly recognized to be a multisystem disorder which includes both clinical and neuropathological features of a frontotemporal lobar degeneration (FTLD). In order to provide a common framework within which to discuss the characteristics of the cognitive and behavioural syndromes of ALS, and with which to conduct clinical and neuropathological research, an international research workshop on frontotemporal dementia (FTD) and ALS was held in London, Canada in June 2007. The recommendations arising from this research workshop address the requirement for a concise clinical diagnosis of the underlying motor neuron disease (Axis I), defining the cognitive and behavioural dysfunction (Axis II), describing additional non-motor manifestations (Axis III) and identifying the presence of disease modifiers (Axis IV).</description><subject>Amyotrophic Lateral Sclerosis - complications</subject><subject>Amyotrophic Lateral Sclerosis - pathology</subject><subject>Amyotrophic Lateral Sclerosis - physiopathology</subject><subject>Cognition Disorders - diagnosis</subject><subject>Cognition Disorders - etiology</subject><subject>Cognition Disorders - pathology</subject><subject>Consensus</subject><subject>dementia</subject><subject>Dementia - diagnosis</subject><subject>Dementia - etiology</subject><subject>Dementia - pathology</subject><subject>Disease Progression</subject><subject>Genetics</subject><subject>Humans</subject><subject>Mental Disorders - diagnosis</subject><subject>Mental Disorders - etiology</subject><subject>Mental Disorders - pathology</subject><subject>neuropathology</subject><issn>1748-2968</issn><issn>1471-180X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1rFTEUhgdRbK3-ADeSlbvRJJOPCbqRi19Q6KYFd-HcTNJJySTXJFO5-OfN5V4QEdpVDpznfUnydN1rgt8RPOL3RLKRKtFGKjgbBHvSnRMmSU9G_ONpm9u-b8B41r0o5Q5jThWlz7szopignA7n3e9NisXGshZksq82e0AuZVRniyYPtzEVX1ByyOUUa6p22aUMAZl0G3319xZBnNDWznDv03rYlH2cclpsQT4iWPap5rSbvUEBWv0BMMHmQ-3L7pmDUOyr03nR3Xz5fL351l9eff2--XTZGzbw2hs3YbAgGB9AykEpMfFBTYpY5owRjBIs-LB1SiohuVDcjIYYCQYwULF1w0X39ti7y-nnakvViy_GhgDRprVoIakUIxaPghQLpuQoG0iOoGkPKdk6vct-gbzXBOuDGv2fmpZ5cypft4ud_iZOLhrw8Qj42Aws8CvlMOkK-5CyyxCNL3p4qP_DP_HZQqizgWz1XTMT2w8_cLs_u6GyBg</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Strong, Michael J.</creator><creator>Grace, Gloria M.</creator><creator>Freedman, Morris</creator><creator>Lomen-Hoerth, Cathy</creator><creator>Woolley, Susan</creator><creator>Goldstein, Laura H.</creator><creator>Murphy, Jennifer</creator><creator>Shoesmith, Christen</creator><creator>Rosenfeld, Jeffery</creator><creator>Leigh, P. Nigel</creator><creator>Bruijn, Lucie</creator><creator>Ince, Paul</creator><creator>Figlewicz, Denise</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>20090101</creationdate><title>Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis</title><author>Strong, Michael J. ; Grace, Gloria M. ; Freedman, Morris ; Lomen-Hoerth, Cathy ; Woolley, Susan ; Goldstein, Laura H. ; Murphy, Jennifer ; Shoesmith, Christen ; Rosenfeld, Jeffery ; Leigh, P. 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In order to provide a common framework within which to discuss the characteristics of the cognitive and behavioural syndromes of ALS, and with which to conduct clinical and neuropathological research, an international research workshop on frontotemporal dementia (FTD) and ALS was held in London, Canada in June 2007. The recommendations arising from this research workshop address the requirement for a concise clinical diagnosis of the underlying motor neuron disease (Axis I), defining the cognitive and behavioural dysfunction (Axis II), describing additional non-motor manifestations (Axis III) and identifying the presence of disease modifiers (Axis IV).</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>19462523</pmid><doi>10.1080/17482960802654364</doi><tpages>16</tpages></addata></record> |
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subjects | Amyotrophic Lateral Sclerosis - complications Amyotrophic Lateral Sclerosis - pathology Amyotrophic Lateral Sclerosis - physiopathology Cognition Disorders - diagnosis Cognition Disorders - etiology Cognition Disorders - pathology Consensus dementia Dementia - diagnosis Dementia - etiology Dementia - pathology Disease Progression Genetics Humans Mental Disorders - diagnosis Mental Disorders - etiology Mental Disorders - pathology neuropathology |
title | Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis |
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