Targeted assessment of lower motor neuron burden is associated with survival in amyotrophic lateral sclerosis. (Q41024423)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26700804%20AND%20SRC:MED&resulttype=core&format=json

3 March 2020

title

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

1 reference

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amyotrophic lateral sclerosis

3 March 2020

main subject

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author

Emma Ballard

2

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3 March 2020

Pamela A. McCombe

5

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3 March 2020

author name string

Matthew S Devine

1

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3 March 2020

Peter O'Rourke

3

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3 March 2020

Robert D Henderson

6

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3 March 2020

Matthew C Kiernan

4

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3 March 2020

language of work or name

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24 December 2015

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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

3 March 2020

published in

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3 March 2020

volume

17

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3 March 2020

issue

3-4

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3 March 2020

page(s)

184-190

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Amyotrophic lateral sclerosis

3 March 2020

cites work

1 reference

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Controversies and priorities in amyotrophic lateral sclerosis

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Patients who survive 5 years or more with ALS in Olmsted County, 1925-2004

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Onset and spreading patterns of lower motor neuron involvements predict survival in sporadic amyotrophic lateral sclerosis

21 January 2018

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Survival and prognostic factors of motor neuron disease in a multi-ethnic Asian population

21 January 2018

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Long-term survival in amyotrophic lateral sclerosis: a population-based study

21 January 2018

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Predicting survival of patients with amyotrophic lateral sclerosis at presentation: a 15-year experience

21 January 2018

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Association of smoking with amyotrophic lateral sclerosis risk and survival in men and women: a prospective study

21 January 2018

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The phenotypic variability of amyotrophic lateral sclerosis

21 January 2018

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Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study

21 January 2018

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Effects of gender in amyotrophic lateral sclerosis

21 January 2018

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Identifying who will benefit from non-invasive ventilation in amyotrophic lateral sclerosis/motor neurone disease in a clinical cohort

21 January 2018

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Mechanisms, models and biomarkers in amyotrophic lateral sclerosis

21 January 2018

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Natural history of amyotrophic lateral sclerosis in a database population Validation of a scoring system and a model for survival prediction

21 January 2018

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Focality of upper and lower motor neuron degeneration at the clinical onset of ALS.

21 January 2018

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El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

21 January 2018

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Clinical trials in amyotrophic lateral sclerosis: why so many negative trials and how can trials be improved?

21 January 2018

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Use of clinical staging in amyotrophic lateral sclerosis for phase 3 clinical trials

21 January 2018

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Development and evaluation of a clinical staging system for amyotrophic lateral sclerosis

21 January 2018

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Regional spread pattern predicts survival in patients with sporadic amyotrophic lateral sclerosis.

21 January 2018

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Why are upper motor neuron signs difficult to elicit in amyotrophic lateral sclerosis?

21 January 2018

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Association of paraspinal and diaphragm denervation in ALS

21 January 2018

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Uncovering amyotrophic lateral sclerosis phenotypes: Clinical features and long-term follow-up of upper motor neuron-dominant ALS

21 January 2018

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A post hoc analysis of subgroup outcomes and creatinine in the phase III clinical trial (EMPOWER) of dexpramipexole in ALS

21 January 2018

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https://api.crossref.org/works/10.3109%2F21678421.2015.1125502

Diaphragmatic dysfunction and dyspnoea in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F21678421.2015.1125502

10.3109/21678421.2015.1125502

21 January 2018

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26700804%20AND%20SRC:MED&resulttype=core&format=json

3 March 2020

1 reference