Update on recent advances in amyotrophic lateral sclerosis
In the last few years, our understanding of disease molecular mechanisms underpinning ALS has advanced greatly, allowing the first steps in translating into clinical practice novel research findings, including gene therapy approaches. Similarly, the recent advent of assistive technologies has greatl...
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Veröffentlicht in: | Journal of neurology 2024-07, Vol.271 (7), p.4693-4723 |
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creator | Riva, Nilo Domi, Teuta Pozzi, Laura Lunetta, Christian Schito, Paride Spinelli, Edoardo Gioele Cabras, Sara Matteoni, Enrico Consonni, Monica Bella, Eleonora Dalla Agosta, Federica Filippi, Massimo Calvo, Andrea Quattrini, Angelo |
description | In the last few years, our understanding of disease molecular mechanisms underpinning ALS has advanced greatly, allowing the first steps in translating into clinical practice novel research findings, including gene therapy approaches. Similarly, the recent advent of assistive technologies has greatly improved the possibility of a more personalized approach to supportive and symptomatic care, in the context of an increasingly complex multidisciplinary line of actions, which remains the cornerstone of ALS management. Against this rapidly growing background, here we provide an comprehensive update on the most recent studies that have contributed towards our understanding of ALS pathogenesis, the latest results from clinical trials as well as the future directions for improving the clinical management of ALS patients. |
doi_str_mv | 10.1007/s00415-024-12435-9 |
format | Article |
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Similarly, the recent advent of assistive technologies has greatly improved the possibility of a more personalized approach to supportive and symptomatic care, in the context of an increasingly complex multidisciplinary line of actions, which remains the cornerstone of ALS management. Against this rapidly growing background, here we provide an comprehensive update on the most recent studies that have contributed towards our understanding of ALS pathogenesis, the latest results from clinical trials as well as the future directions for improving the clinical management of ALS patients.</description><identifier>ISSN: 0340-5354</identifier><identifier>ISSN: 1432-1459</identifier><identifier>EISSN: 1432-1459</identifier><identifier>DOI: 10.1007/s00415-024-12435-9</identifier><identifier>PMID: 38802624</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Amyotrophic lateral sclerosis ; Amyotrophic Lateral Sclerosis - genetics ; Amyotrophic Lateral Sclerosis - therapy ; Animals ; Clinical trials ; Females ; Gene therapy ; Humans ; Kinases ; Life expectancy ; Males ; Medical imaging ; Medical prognosis ; Medicine ; Medicine & Public Health ; Molecular modelling ; Motor neurone disease ; Mutation ; Neuroimaging ; Neurological Update ; Neurology ; Neuroradiology ; Neurosciences ; Pathogenesis</subject><ispartof>Journal of neurology, 2024-07, Vol.271 (7), p.4693-4723</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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Similarly, the recent advent of assistive technologies has greatly improved the possibility of a more personalized approach to supportive and symptomatic care, in the context of an increasingly complex multidisciplinary line of actions, which remains the cornerstone of ALS management. Against this rapidly growing background, here we provide an comprehensive update on the most recent studies that have contributed towards our understanding of ALS pathogenesis, the latest results from clinical trials as well as the future directions for improving the clinical management of ALS patients.</description><subject>Amyotrophic lateral sclerosis</subject><subject>Amyotrophic Lateral Sclerosis - genetics</subject><subject>Amyotrophic Lateral Sclerosis - therapy</subject><subject>Animals</subject><subject>Clinical trials</subject><subject>Females</subject><subject>Gene therapy</subject><subject>Humans</subject><subject>Kinases</subject><subject>Life expectancy</subject><subject>Males</subject><subject>Medical imaging</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Molecular modelling</subject><subject>Motor neurone disease</subject><subject>Mutation</subject><subject>Neuroimaging</subject><subject>Neurological Update</subject><subject>Neurology</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Pathogenesis</subject><issn>0340-5354</issn><issn>1432-1459</issn><issn>1432-1459</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><recordid>eNp9kTtPxDAQhC0EguPgD1CgSDQ0gV2_ktAghHhJSDRcbTnOHgTl4sPOIfHv8XG8CyoX--14ZoexPYQjBCiOI4BElQOXOXIpVF6tsRFKwXOUqlpnIxASciWU3GLbMT4BQJkGm2xLlCVwzeWInUzmjR0o830WyFE_ZLZ5sb2jmLV9Zmevfgh-_ti6rEtYsF0WXUfBxzbusI2p7SLtfrxjNrm8uD-_zm_vrm7Oz25zJ5Qe8hJJkLR2KotK105qlHVVopYClC5Q1SVyBKWaoiZ0stKkRE0NUiUaWfNKjNnpSne-qGfULE0mH2Ye2pkNr8bb1vye9O2jefAvBpELITQkhcMPheCfFxQHM2ujo66zPflFNAI0YjIry4Qe_EGf_CL0KV-iikIVmE6XKL6iXLpEDDT9coNglt2YVTcmdWPeuzHLHPs_c3ytfJaRALECYhr1DxS-__5H9g0-Zpjn</recordid><startdate>202407</startdate><enddate>202407</enddate><creator>Riva, Nilo</creator><creator>Domi, Teuta</creator><creator>Pozzi, Laura</creator><creator>Lunetta, Christian</creator><creator>Schito, Paride</creator><creator>Spinelli, Edoardo Gioele</creator><creator>Cabras, Sara</creator><creator>Matteoni, Enrico</creator><creator>Consonni, Monica</creator><creator>Bella, Eleonora Dalla</creator><creator>Agosta, Federica</creator><creator>Filippi, Massimo</creator><creator>Calvo, Andrea</creator><creator>Quattrini, Angelo</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><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>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0513-9517</orcidid></search><sort><creationdate>202407</creationdate><title>Update on recent advances in amyotrophic lateral sclerosis</title><author>Riva, Nilo ; 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subjects | Amyotrophic lateral sclerosis Amyotrophic Lateral Sclerosis - genetics Amyotrophic Lateral Sclerosis - therapy Animals Clinical trials Females Gene therapy Humans Kinases Life expectancy Males Medical imaging Medical prognosis Medicine Medicine & Public Health Molecular modelling Motor neurone disease Mutation Neuroimaging Neurological Update Neurology Neuroradiology Neurosciences Pathogenesis |
title | Update on recent advances in amyotrophic lateral sclerosis |
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