Targeted assessment of lower motor neuron burden is associated with survival in amyotrophic lateral sclerosis

No abstract is available for this paper.

• Publication year

  2016

• Venue

  Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

• Publication date

  2016-05-18

• Fields of study

  Medicine

• Identifiers
  DOI 10.3109/21678421.2015.1125502PMID 26700804
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• The phenotypic variability of amyotrophic lateral sclerosis

  2014cited by this paper
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  2014cited by this paper
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  2013cited by this paper
• of amyotrophic lateral sclerosis

  2013cited by this paper
• Controversies and priorities in amyotrophic lateral sclerosis.

  2013influential reference
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  2013cited by this paper
• Phrenic nerve studies predict survival in amyotrophic lateral sclerosis.

  2012cited by this paper
• Reduction rate of body mass index predicts prognosis for survival in amyotrophic lateral sclerosis: A multicenter study in Japan

  2012cited by this paper
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  2011cited by this paper
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  2011cited by this paper
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  2011cited by this paper
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  2011cited by this paper
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  2010cited by this paper
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  2010cited by this paper
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• Prognostic factors in ALS: A critical review

  2009influential reference
• Clinical phenotypes and natural progression for motor neuron disease: Analysis from an Australian database

  2009cited by this paper
• Predictors of long survival in amyotrophic lateral sclerosis: a population-based study.

  2008cited by this paper
• [Pronostic factors and survival in motor neuron disease].

  2007cited by this paper
• Focality of upper and lower motor neuron degeneration at the clinical onset of ALS

  2007influential reference
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  2007cited by this paper
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  1995cited by this paper
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  1988cited by this paper

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  2024cites this paper
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  2024cites this paper
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  2023cites this paper
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  2023cites this paper
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  2023cites this paper
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  2023influential citation
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  2023cites this paper
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  2023cites this paper
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  2022cites this paper
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  2018cites this paper
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