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Long‐term edaravone efficacy in amyotrophic lateral sclerosis: Post‐hoc analyses of Study 19 (MCI186‐19)

Muscle & nerve, 2020-02, Vol.61 (2), p.218-221

2020

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Categorization of the amyotrophic lateral sclerosis population via the clinical determinant of post‐onset ΔFS for study design and medical practice

Muscle & nerve, 2024-07, Vol.70 (1), p.36-41

2024

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Real-world evidence of riluzole effectiveness in treating amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2020-10, Vol.21 (7-8), p.509-518

2020

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Multidisciplinary Clinics in Neuromuscular Medicine

Continuum (Minneapolis, Minn.), 2023-10, Vol.29 (5), p.1585-1594

2023

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Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease

PloS one, 2022-09, Vol.17 (9), p.e0274615-e0274615

2022

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Effect of sodium phenylbutyrate/taurursodiol on tracheostomy/ventilation-free survival and hospitalisation in amyotrophic lateral sclerosis: long-term results from the CENTAUR trial

Journal of neurology, neurosurgery and psychiatry, 2022-08, Vol.93 (8), p.871-875

2022

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Primary lateral sclerosis (PLS) functional rating scale: PLS‐specific clinimetric scale

Muscle & nerve, 2020-02, Vol.61 (2), p.163-172

2020

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Hypercaloric enteral nutrition in patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled phase 2 trial

The Lancet (British edition), 2014-06, Vol.383 (9934), p.2065-2072

2014

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Hereditary spastic paraplegia: gain-of-function mechanisms revealed by new transgenic mouse

Human molecular genetics, 2019-04, Vol.28 (7), p.1136-1152

2019

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Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron disease

PloS one, 2015-03, Vol.10 (3), p.e0117848-e0117848

2015

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Phase II trial of CoQ10 for ALS finds insufficient evidence to justify phase III

Annals of neurology, 2009-08, Vol.66 (2), p.235-244

2009

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Charcot–Marie–Tooth Disease type 4C: Novel mutations, clinical presentations, and diagnostic challenges

Muscle & nerve, 2018-05, Vol.57 (5), p.749-755

2018

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Phenotype of transgenic mice carrying a very low copy number of the mutant human G93A superoxide dismutase-1 gene associated with amyotrophic lateral sclerosis

PloS one, 2014-06, Vol.9 (6), p.e99879-e99879

2014

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Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy

Neurogenetics, 2015-01, Vol.16 (1), p.1-9

2015

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Understanding the use of NIV in ALS: results of an international ALS specialist survey

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2018-07, Vol.19 (5-6), p.331-341

2018

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Edaravone efficacy in amyotrophic lateral sclerosis with reduced forced vital capacity: Post-hoc analysis of Study 19 (MCI186-19) [clinical trial NCT01492686]

PloS one, 2022-06, Vol.17 (6), p.e0258614-e0258614

2022

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Pulmonary function decline in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2021-07, Vol.22 (S1), p.54-61

2021

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Use of a new ALS specific respiratory questionnaire: the ARES score

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2021-07, Vol.22 (S1), p.48-53

2021

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Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease

PloS one, 2022-09, Vol.17 (9)

2022

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A Review of Economic Studies of Amyotrophic Lateral Sclerosis (ALS) in the United States (P3-8.015)

Neurology, 2023-04, Vol.100 (17_supplement_2)

2023

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Evaluation of Gastrointestinal Symptoms in an ALS Cohort (P10-8.007)

Neurology, 2023-04, Vol.100 (17_supplement_2)

2023

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Unconscious homophobia and the rise of the transgender movement

Psychodynamic practice, 2018-01, Vol.24 (1), p.56-59

Patterson, Terry

2018

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NIPPV: a treatment for ALS whose time has come

Neurology, 2006-09, Vol.67 (5), p.736-737

2006

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Deep hypothermic circulatory arrest: I. Effects of cooling on electroencephalogram and evoked potentials

The Annals of thoracic surgery, 2001, Vol.71 (1), p.14-21

2001

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A major QTL on mouse chromosome 17 resulting in lifespan variability in SOD1-G93A transgenic mouse models of amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2014-12, Vol.15 (7-8), p.588-600

2014

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Long‐term edaravone efficacy in amyotrophic lateral sclerosis: Post‐hoc analyses of Study 19 (MCI186‐19)

Categorization of the amyotrophic lateral sclerosis population via the clinical determinant of post‐onset ΔFS for study design and medical practice

Real-world evidence of riluzole effectiveness in treating amyotrophic lateral sclerosis

Multidisciplinary Clinics in Neuromuscular Medicine

Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease

Effect of sodium phenylbutyrate/taurursodiol on tracheostomy/ventilation-free survival and hospitalisation in amyotrophic lateral sclerosis: long-term results from the CENTAUR trial

Primary lateral sclerosis (PLS) functional rating scale: PLS‐specific clinimetric scale

Hypercaloric enteral nutrition in patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled phase 2 trial

Hereditary spastic paraplegia: gain-of-function mechanisms revealed by new transgenic mouse

Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron disease

Phase II trial of CoQ10 for ALS finds insufficient evidence to justify phase III

Charcot–Marie–Tooth Disease type 4C: Novel mutations, clinical presentations, and diagnostic challenges

Phenotype of transgenic mice carrying a very low copy number of the mutant human G93A superoxide dismutase-1 gene associated with amyotrophic lateral sclerosis

Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy

Understanding the use of NIV in ALS: results of an international ALS specialist survey

Edaravone efficacy in amyotrophic lateral sclerosis with reduced forced vital capacity: Post-hoc analysis of Study 19 (MCI186-19) [clinical trial NCT01492686]

Pulmonary function decline in amyotrophic lateral sclerosis

Use of a new ALS specific respiratory questionnaire: the ARES score

Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease

A Review of Economic Studies of Amyotrophic Lateral Sclerosis (ALS) in the United States (P3-8.015)

Evaluation of Gastrointestinal Symptoms in an ALS Cohort (P10-8.007)

Unconscious homophobia and the rise of the transgender movement

NIPPV: a treatment for ALS whose time has come

Deep hypothermic circulatory arrest: I. Effects of cooling on electroencephalogram and evoked potentials

A major QTL on mouse chromosome 17 resulting in lifespan variability in SOD1-G93A transgenic mouse models of amyotrophic lateral sclerosis

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