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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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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. |
format | Online Article Text |
id | pubmed-4893385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
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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