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Supportive and symptomatic management of amyotrophic lateral sclerosis

Nature reviews. Neurology, 2016-09, Vol.12 (9), p.526

2016

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Trial of Antisense Oligonucleotide Tofersen for SOD1 ALS

The New England journal of medicine, 2022-09, Vol.387 (12), p.1099-1110

2022

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Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72

Brain (London, England : 1878), 2012-03, Vol.135 (Pt 3), p.751-764

2012

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An Objective Functional Characterisation of Head Movement Impairment in Individuals with Neck Muscle Weakness Due to Amyotrophic Lateral Sclerosis

PloS one, 2017-01, Vol.12 (1), p.e0169019-e0169019

2017

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Decision-making and referral processes for patients with motor neurone disease: a qualitative study of GP experiences and evaluation of a new decision-support tool

BMC health services research, 2017-05, Vol.17 (1), p.339-339, Article 339

2017

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Gastrostomy in amyotrophic lateral sclerosis: effects of non-invasive ventilation – Authors' reply

Lancet neurology, 2015-12, Vol.14 (12), p.1153-1153

2015

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Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients

Journal of neurochemistry, 2009-07, Vol.110 (1), p.34-44

2009

Volltextzugriff (PDF)

Do pain, anxiety and depression influence quality of life for people with amyotrophic lateral sclerosis/motor neuron disease? A national study reconciling previous conflicting literature

Journal of neurology, 2020-03, Vol.267 (3), p.607-615

2020

Volltextzugriff (PDF)

European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERN EURO‐NMD)

European journal of neurology, 2024-06, Vol.31 (6), p.e16264-n/a

2024

Volltextzugriff (PDF)

Process evaluation and exploration of telehealth in motor neuron disease in a UK specialist centre

BMJ open, 2019-10, Vol.9 (10), p.e028526-e028526

2019

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Non-invasive ventilation in motor neuron disease: an update of current UK practice

Journal of neurology, neurosurgery and psychiatry, 2012-04, Vol.83 (4), p.371-376

2012

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Identifying key signs of motor neurone disease in primary care: a nested case–control study using the QResearch database

BMJ open, 2022-06, Vol.12 (6), p.e058383-e058383

2022

Volltextzugriff (PDF)

Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease

Journal of neurology, 2020-01, Vol.267 (1), p.244-256

2020

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Diaphragm pacing in patients with amyotrophic lateral sclerosis – Authors' reply

Lancet neurology, 2016-05, Vol.15 (6), p.543-544

2016

Volltextzugriff (PDF)

The application of Raman spectroscopy to the diagnosis of mitochondrial muscle disease: A preliminary comparison between fibre optic probe and microscope formats

Journal of Raman spectroscopy, 2022-02, Vol.53 (2), p.172-181

2022

Volltextzugriff (PDF)

Using telehealth in motor neuron disease to increase access to specialist multidisciplinary care: a UK-based pilot and feasibility study

BMJ open, 2019-10, Vol.9 (10), p.e028525

2019

Volltextzugriff (PDF)

C9ORF72 expansions, parkinsonism, and Parkinson disease: a clinicopathologic study

Neurology, 2013-08, Vol.81 (9), p.808

2013

Volltextzugriff (PDF)

Concurrence of multiple sclerosis and amyotrophic lateral sclerosis in patients with hexanucleotide repeat expansions of C9ORF72

Journal of neurology, neurosurgery and psychiatry, 2013-01, Vol.84 (1), p.79-87

2013

Volltextzugriff (PDF)

Correction to: Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease

Journal of neurology, 2020, Vol.267 (1), p.257-258

2020

Volltextzugriff (PDF)

Developing a web-based patient decision aid for gastrostomy in motor neuron disease: a study protocol

BMJ open, 2019-12, Vol.9 (12), p.e032364-e032364

2019

Volltextzugriff (PDF)

Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis

Neurogenetics, 2010-05, Vol.11 (2), p.217-225

2010

Volltextzugriff (PDF)

Hereditary spastic paraparesis: Disrupted intracellular transport associated with spastin mutation

Annals of neurology, 2003-12, Vol.54 (6), p.748-759

2003

Volltextzugriff (PDF)

New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP)

Neurogenetics, 2009-04, Vol.10 (2), p.105-110

2009

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Respiratory management of motor neurone disease: a review of current practice and new developments

Practical Neurology, 2012-06, Vol.12 (3), p.166-176

2012

Volltextzugriff (PDF)

Gastrostomy in patients with amyotrophic lateral sclerosis (ProGas): a prospective cohort study

Lancet neurology, 2015-07, Vol.14 (7), p.702-709

Anon

2015

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Supportive and symptomatic management of amyotrophic lateral sclerosis

Trial of Antisense Oligonucleotide Tofersen for SOD1 ALS

Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72

An Objective Functional Characterisation of Head Movement Impairment in Individuals with Neck Muscle Weakness Due to Amyotrophic Lateral Sclerosis

Decision-making and referral processes for patients with motor neurone disease: a qualitative study of GP experiences and evaluation of a new decision-support tool

Gastrostomy in amyotrophic lateral sclerosis: effects of non-invasive ventilation – Authors' reply

Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients

Do pain, anxiety and depression influence quality of life for people with amyotrophic lateral sclerosis/motor neuron disease? A national study reconciling previous conflicting literature

European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERN EURO‐NMD)

Process evaluation and exploration of telehealth in motor neuron disease in a UK specialist centre

Non-invasive ventilation in motor neuron disease: an update of current UK practice

Identifying key signs of motor neurone disease in primary care: a nested case–control study using the QResearch database

Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease

Diaphragm pacing in patients with amyotrophic lateral sclerosis – Authors' reply

The application of Raman spectroscopy to the diagnosis of mitochondrial muscle disease: A preliminary comparison between fibre optic probe and microscope formats

Using telehealth in motor neuron disease to increase access to specialist multidisciplinary care: a UK-based pilot and feasibility study

C9ORF72 expansions, parkinsonism, and Parkinson disease: a clinicopathologic study

Concurrence of multiple sclerosis and amyotrophic lateral sclerosis in patients with hexanucleotide repeat expansions of C9ORF72

Correction to: Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease

Developing a web-based patient decision aid for gastrostomy in motor neuron disease: a study protocol

Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis

Hereditary spastic paraparesis: Disrupted intracellular transport associated with spastin mutation

New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP)

Respiratory management of motor neurone disease: a review of current practice and new developments

Gastrostomy in patients with amyotrophic lateral sclerosis (ProGas): a prospective cohort study

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