<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Benatar M</submitter><funding>Brain Research UK</funding><funding>NIA NIH HHS</funding><funding>The ALS Association</funding><funding>Medical Research Council</funding><funding>National Institute for Health Research (NIHR)</funding><funding>Motor Neurone Disease Association</funding><funding>NINDS NIH HHS</funding><funding>National Institutes of Health</funding><funding>The Muscular Dystrophy Association</funding><funding>The Motor Neurone Disease Association</funding><funding>The Association for Frontotemporal Degeneration, Biogen and AveXis</funding><pagination>27-44</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8967095</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>145(1)</volume><pubmed_abstract>Significant progress has been made in understanding the pre-symptomatic phase of amyotrophic lateral sclerosis. While much is still unknown, advances in other neurodegenerative diseases offer valuable insights. Indeed, it is increasingly clear that the well-recognized clinical syndromes of Alzheimer's disease, Parkinson's disease, Huntington's disease, spinal muscular atrophy and frontotemporal dementia are also each preceded by a pre-symptomatic or prodromal period of varying duration, during which the underlying disease process unfolds, with associated compensatory changes and loss of inherent system redundancy. Key insights from these diseases highlight opportunities for discovery in amyotrophic lateral sclerosis. The development of biomarkers reflecting amyloid and tau has led to a shi</pubmed_abstract><journal>Brain : a journal of neurology</journal><pubmed_title>Preventing amyotrophic lateral sclerosis: insights from pre-symptomatic neurodegenerative diseases.</pubmed_title><pmcid>PMC8967095</pmcid><funding_grant_id>NIHR202421</funding_grant_id><funding_grant_id>U54 NS092091</funding_grant_id><funding_grant_id>MR/M023664/1</funding_grant_id><funding_grant_id>MR/J009482/1</funding_grant_id><funding_grant_id>P30 AG062677</funding_grant_id><funding_grant_id>ALCHALABI-TALBOT/APR14/926-794</funding_grant_id><funding_grant_id>U01 AG006786</funding_grant_id><funding_grant_id>P01 AG019724</funding_grant_id><funding_grant_id>MR/L501529/1</funding_grant_id><funding_grant_id>TURNER/OCT18/989-797</funding_grant_id><funding_grant_id>R01 NS105479</funding_grant_id><funding_grant_id>MR/M008525/1</funding_grant_id><funding_grant_id>MR/T046015/1</funding_grant_id><funding_grant_id>G0600974</funding_grant_id><funding_grant_id>TURNER/JAN13/944-795</funding_grant_id><funding_grant_id>ALCHALABI-DOBSON/APR14/829-791</funding_grant_id><funding_grant_id>MR/R024804/1</funding_grant_id><funding_grant_id>202021-32</funding_grant_id><funding_grant_id>Al-Chalabi/Apr19/870-791</funding_grant_id><pubmed_authors>Lee S</pubmed_authors><pubmed_authors>Thakur N</pubmed_authors><pubmed_authors>Benatar M</pubmed_authors><pubmed_authors>McMillan CT</pubmed_authors><pubmed_authors>Postuma RB</pubmed_authors><pubmed_authors>Stanislaw C</pubmed_authors><pubmed_authors>Le Ber I</pubmed_authors><pubmed_authors>Gendron T</pubmed_authors><pubmed_authors>McHutchison C</pubmed_authors><pubmed_authors>Andersen PM</pubmed_authors><pubmed_authors>Ross CA</pubmed_authors><pubmed_authors>Turner M</pubmed_authors><pubmed_authors>Floeter MK</pubmed_authors><pubmed_authors>Gubitz A</pubmed_authors><pubmed_authors>Boeve BF</pubmed_authors><pubmed_authors>Cosentino S</pubmed_authors><pubmed_authors>First International Pre-Symptomatic ALS Workshop</pubmed_authors><pubmed_authors>Rohrer J</pubmed_authors><pubmed_authors>Arias JJ</pubmed_authors><pubmed_authors>Abrahams S</pubmed_authors><pubmed_authors>Grignon AL</pubmed_authors><pubmed_authors>Ross C</pubmed_authors><pubmed_authors>Dave K</pubmed_authors><pubmed_authors>Wuu J</pubmed_authors><pubmed_authors>Boeve B</pubmed_authors><pubmed_authors>Fradette S</pubmed_authors><pubmed_authors>Malaspina A</pubmed_authors><pubmed_authors>McMillan C</pubmed_authors><pubmed_authors>Shefner J</pubmed_authors><pubmed_authors>Rohrer JD</pubmed_authors><pubmed_authors>Granit V</pubmed_authors><pubmed_authors>Arias J</pubmed_authors><pubmed_authors>Nicholson K</pubmed_authors><pubmed_authors>Turner MR</pubmed_authors><pubmed_authors>Ferguson T</pubmed_authors><pubmed_authors>Rosen H</pubmed_authors><pubmed_authors>Robinson R</pubmed_authors><pubmed_authors>Finkel RS</pubmed_authors><pubmed_authors>Weishaupt J</pubmed_authors><pubmed_authors>Kaufman P</pubmed_authors><pubmed_authors>Grossman M</pubmed_authors><pubmed_authors>Tatton N</pubmed_authors><pubmed_authors>McDermott MP</pubmed_authors><pubmed_authors>Al-Chalabi A</pubmed_authors><pubmed_authors>Postuma R</pubmed_authors><pubmed_authors>Petersen R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Preventing amyotrophic lateral sclerosis: insights from pre-symptomatic neurodegenerative diseases.</name><description>Significant progress has been made in understanding the pre-symptomatic phase of amyotrophic lateral sclerosis. While much is still unknown, advances in other neurodegenerative diseases offer valuable insights. Indeed, it is increasingly clear that the well-recognized clinical syndromes of Alzheimer's disease, Parkinson's disease, Huntington's disease, spinal muscular atrophy and frontotemporal dementia are also each preceded by a pre-symptomatic or prodromal period of varying duration, during which the underlying disease process unfolds, with associated compensatory changes and loss of inherent system redundancy. Key insights from these diseases highlight opportunities for discovery in amyotrophic lateral sclerosis. The development of biomarkers reflecting amyloid and tau has led to a shi</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-05T15:59:33.958Z</modification><creation>2025-04-05T15:59:33.958Z</creation></dates><accession>S-EPMC8967095</accession><cross_references><pubmed>34677606</pubmed><doi>10.1093/brain/awab404</doi></cross_references></HashMap>