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Estimating clinical stage of amyotrophic lateral sclerosis from the ALS Functional Rating Scale

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2014-06, Vol.15 (3-4), p.279-284

2014

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The evaluation of pain in amyotrophic lateral sclerosis: A case controlled observational study

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2014-12, Vol.15 (7-8), p.520-527

2014

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Autosomal dominant inheritance of rapidly progressive amyotrophic lateral sclerosis due to a truncation mutation in the fused in sarcoma (FUS) gene

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2014-12, Vol.15 (7-8), p.557-562

2014

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SOD1-ALS-Browser: a web-utility for investigating the clinical phenotype in SOD1 amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2023-10, Vol.24 (7-8), p.1-745

2023

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pNfH is a promising biomarker for ALS

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2013-03, Vol.14 (2), p.146-149

2013

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The use of biotelemetry to explore disease progression markers in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2020-10, Vol.21 (7-8), p.563-573

2020

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The benefit of evolving multidisciplinary care in ALS: a diagnostic cohort survival comparison

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2017-10, Vol.18 (7-8), p.569-575

2017

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Telomere length is greater in ALS than in controls: a whole genome sequencing study

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2019-04, Vol.20 (3-4), p.229-234

2019

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Predicting the future of ALS: the impact of demographic change and potential new treatments on the prevalence of ALS in the United Kingdom, 2020-2116

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2019-04, Vol.20 (3-4), p.264-274

2019

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Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2016-11, Vol.17 (7-8), p.593-599

2016

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Psychological as well as illness factors influence acceptance of non-invasive ventilation (NIV) and gastrostomy in amyotrophic lateral sclerosis (ALS): A prospective population study

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2014-09, Vol.15 (5-6), p.376-387

2014

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Unpicking neurodegeneration in a dish with human pluripotent stem cells: One cell type at a time

Cell cycle (Georgetown, Tex.), 2013-08, Vol.12 (15), p.2339-2340

2013

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Impact of disease, cognitive and behavioural factors on caregiver outcome in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2015-08, Vol.16 (5-6), p.316-323

2015

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Evidence of an environmental effect on survival in ALS

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2014-12, Vol.15 (7-8), p.528-533

2014

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Regionality of disease progression predicts prognosis in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2015-11, Vol.16 (7-8), p.442-447

2015

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The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2019-07, Vol.20 (5-6), p.432-440

2019

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Eating-derived pleasure in amyotrophic lateral sclerosis as a predictor of non-oral feeding

Amyotrophic lateral sclerosis, 2012-10, Vol.13 (6), p.555-559

2012

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No evidence for a large difference in ALS frequency in populations of African and European origin: A population based study in inner city London

Amyotrophic lateral sclerosis, 2012-01, Vol.13 (1), p.66-68

2012

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The association between ALS and population density: A population based study

Amyotrophic lateral sclerosis, 2010-10, Vol.11 (5), p.435-438

2010

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Survival of patients with ALS following institution of enteral feeding is related to pre-procedure oximetry: A retrospective review of 98 patients in a single centre

Amyotrophic lateral sclerosis, 2006-03, Vol.7 (1), p.16-21

2006

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Volumetric cortical loss in sporadic and familial amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis, 2007-01, Vol.8 (6), p.343-347

2007

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Identified with the one: Edward Carpenter, Henry Salt and the ethical socialist philosophy of science

Prose studies, 1990-05, Vol.13 (1), p.33-57

Shaw, Christopher E.

1990

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Association study on glutathione S-transferase omega 1 and 2 and familial ALS

Amyotrophic lateral sclerosis, 2008, Vol.9 (2), p.81-84

2008

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A common haplotype within the PON1 promoter region is associated with sporadic ALS

Amyotrophic lateral sclerosis, 2008-01, Vol.9 (5), p.306-314

2008

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Using Community-Based Participatory Research to Disseminate a Mass Media Campaign Into Rural Communities

Journal of health communication, 2015-07, Vol.20 (7), p.799-806

2015

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Estimating clinical stage of amyotrophic lateral sclerosis from the ALS Functional Rating Scale

The evaluation of pain in amyotrophic lateral sclerosis: A case controlled observational study

Autosomal dominant inheritance of rapidly progressive amyotrophic lateral sclerosis due to a truncation mutation in the fused in sarcoma (FUS) gene

SOD1-ALS-Browser: a web-utility for investigating the clinical phenotype in SOD1 amyotrophic lateral sclerosis

pNfH is a promising biomarker for ALS

The use of biotelemetry to explore disease progression markers in amyotrophic lateral sclerosis

The benefit of evolving multidisciplinary care in ALS: a diagnostic cohort survival comparison

Telomere length is greater in ALS than in controls: a whole genome sequencing study

Predicting the future of ALS: the impact of demographic change and potential new treatments on the prevalence of ALS in the United Kingdom, 2020-2116

Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis

Psychological as well as illness factors influence acceptance of non-invasive ventilation (NIV) and gastrostomy in amyotrophic lateral sclerosis (ALS): A prospective population study

Unpicking neurodegeneration in a dish with human pluripotent stem cells: One cell type at a time

Impact of disease, cognitive and behavioural factors on caregiver outcome in amyotrophic lateral sclerosis

Evidence of an environmental effect on survival in ALS

Regionality of disease progression predicts prognosis in amyotrophic lateral sclerosis

The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public

Eating-derived pleasure in amyotrophic lateral sclerosis as a predictor of non-oral feeding

No evidence for a large difference in ALS frequency in populations of African and European origin: A population based study in inner city London

The association between ALS and population density: A population based study

Survival of patients with ALS following institution of enteral feeding is related to pre-procedure oximetry: A retrospective review of 98 patients in a single centre

Volumetric cortical loss in sporadic and familial amyotrophic lateral sclerosis

Identified with the one: Edward Carpenter, Henry Salt and the ethical socialist philosophy of science

Association study on glutathione S-transferase omega 1 and 2 and familial ALS

A common haplotype within the PON1 promoter region is associated with sporadic ALS

Using Community-Based Participatory Research to Disseminate a Mass Media Campaign Into Rural Communities

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