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Recent advances in amyotrophic lateral sclerosis

ALS is a relentlessly progressive and fatal disease, with no curative therapies available to date. Symptomatic and palliative care, provided in a multidisciplinary context, still remains the cornerstone of ALS management. However, our understanding of the molecular mechanisms underlying the disease...

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Autores principales: Riva, Nilo, Agosta, Federica, Lunetta, Christian, Filippi, Massimo, Quattrini, Angelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893385/
https://www.ncbi.nlm.nih.gov/pubmed/27025851
http://dx.doi.org/10.1007/s00415-016-8091-6
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author Riva, Nilo
Agosta, Federica
Lunetta, Christian
Filippi, Massimo
Quattrini, Angelo
author_facet Riva, Nilo
Agosta, Federica
Lunetta, Christian
Filippi, Massimo
Quattrini, Angelo
author_sort Riva, Nilo
collection PubMed
description ALS is a relentlessly progressive and fatal disease, with no curative therapies available to date. Symptomatic and palliative care, provided in a multidisciplinary context, still remains the cornerstone of ALS management. However, our understanding of the molecular mechanisms underlying the disease has advanced greatly over the past years, giving new hope for the development of novel diagnostic and therapeutic approaches. Here, we have reviewed the most recent studies that have contributed to improving both clinical management and our understanding of ALS pathogenesis.
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spelling pubmed-48933852016-06-20 Recent advances in amyotrophic lateral sclerosis Riva, Nilo Agosta, Federica Lunetta, Christian Filippi, Massimo Quattrini, Angelo J Neurol Neurological Update ALS is a relentlessly progressive and fatal disease, with no curative therapies available to date. Symptomatic and palliative care, provided in a multidisciplinary context, still remains the cornerstone of ALS management. However, our understanding of the molecular mechanisms underlying the disease has advanced greatly over the past years, giving new hope for the development of novel diagnostic and therapeutic approaches. Here, we have reviewed the most recent studies that have contributed to improving both clinical management and our understanding of ALS pathogenesis. Springer Berlin Heidelberg 2016-03-30 2016 /pmc/articles/PMC4893385/ /pubmed/27025851 http://dx.doi.org/10.1007/s00415-016-8091-6 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Neurological Update
Riva, Nilo
Agosta, Federica
Lunetta, Christian
Filippi, Massimo
Quattrini, Angelo
Recent advances in amyotrophic lateral sclerosis
title Recent advances in amyotrophic lateral sclerosis
title_full Recent advances in amyotrophic lateral sclerosis
title_fullStr Recent advances in amyotrophic lateral sclerosis
title_full_unstemmed Recent advances in amyotrophic lateral sclerosis
title_short Recent advances in amyotrophic lateral sclerosis
title_sort recent advances in amyotrophic lateral sclerosis
topic Neurological Update
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893385/
https://www.ncbi.nlm.nih.gov/pubmed/27025851
http://dx.doi.org/10.1007/s00415-016-8091-6
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