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The Dying Forward Hypothesis of ALS: Tracing Its History

Brain sciences, 2021-02, Vol.11 (3), p.300

Eisen, Andrew

2021

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Amyotrophic lateral sclerosis: A 40-year personal perspective

Journal of clinical neuroscience, 2009-04, Vol.16 (4), p.505-512

Eisen, Andrew

2009

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Transcranial magnetic stimulation and amyotrophic lateral sclerosis: pathophysiological insights

Journal of Neurology, Neurosurgery and Psychiatry, 2013-10, Vol.84 (10), p.1161-1170

2013

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A proposal for new diagnostic criteria for ALS

Clinical neurophysiology, 2020-08, Vol.131 (8), p.1975-1978

2020

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Amyotrophic lateral sclerosis

The Lancet (British edition), 2011-03, Vol.377 (9769), p.942-955

2011

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Amyotrophic lateral sclerosis: Origins traced to impaired balance between neural excitation and inhibition in the neonatal period

Muscle & nerve, 2019-09, Vol.60 (3), p.232-235

2019

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The strength of corticomotoneuronal drive underlies ALS split phenotypes and reflects early upper motor neuron dysfunction

Brain and behavior, 2021-12, Vol.11 (12), p.e2403-n/a

2021

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Neuronal network disintegration: common pathways linking neurodegenerative diseases

Journal of Neurology, Neurosurgery and Psychiatry, 2016-11, Vol.87 (11), p.1234-1241

2016

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ALS/FTD: Evolution, Aging, and Cellular Metabolic Exhaustion

Frontiers in neurology, 2022-05, Vol.13, p.890203-890203

2022

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History of ALS and the competing theories on pathogenesis: IFCN handbook chapter

Clinical neurophysiology practice, 2024-01, Vol.9, p.1-12

2024

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In Memorium: Jun Kimura, MD

Muscle & nerve, 2022-05, Vol.65 (5), p.487-488

Eisen, Andrew

2022

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Serum MicroRNAs Reflect Injury Severity in a Large Animal Model of Thoracic Spinal Cord Injury

Scientific reports, 2017-05, Vol.7 (1), p.1376-14, Article 1376

2017

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The relationship between personality disorder traits, emotional intelligence, and college adjustment

Journal of clinical psychology, 2018-07, Vol.74 (7), p.1160-1173

2018

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Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p

Acta neuropathologica, 2012-03, Vol.123 (3), p.409-417

2012

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Abstract 4127: RX-5902 exhibits direct and immunomodulatory anti-tumor activities in melanoma PDX models

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.4127-4127

Eisen, Andrew

2019

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RX-5902, a novel β-catenin modulator, potentiates the efficacy of immune checkpoint inhibitors in preclinical models of triple-negative breast Cancer

BMC cancer, 2020-11, Vol.20 (1), p.1063-1063, Article 1063

2020

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Central nervous system in motor neuron disease

Journal of neurology, neurosurgery and psychiatry, 2018-09, Vol.89 (9), p.901-902

Eisen, Andrew

2018

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The split hand syndrome in amyotrophic lateral sclerosis

Journal of Neurology, Neurosurgery and Psychiatry, 2012-04, Vol.83 (4), p.399-403

2012

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Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis

Muscle & nerve, 2010-08, Vol.42 (2), p.170-176

2010

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The motor deficit of ALS reflects failure to generate muscle synergies for complex motor tasks, not just muscle strength

Neuroscience letters, 2021-09, Vol.762, p.136171-136171, Article 136171

2021

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Nanoplastics and Neurodegeneration in ALS

Brain sciences, 2024-05, Vol.14 (5), p.471

2024

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Hypothesis: amyotrophic lateral sclerosis and environmental pollutants

Muscle & nerve, 2020-08, Vol.62 (2), p.187-191

2020

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The impact of respite care from the perspectives and experiences of people with amyotrophic lateral sclerosis and their care partners: a qualitative study

BMC palliative care, 2022-02, Vol.21 (1), p.26-26, Article 26

2022

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The motor cortex and amyotrophic lateral sclerosis

Muscle & nerve, 2001-04, Vol.24 (4), p.564-573

2001

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Amyotrophic lateral sclerosis-Evolutionary and other perspectives

Muscle & nerve, 2009-08, Vol.40 (2), p.297-304

Eisen, Andrew

2009

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The Dying Forward Hypothesis of ALS: Tracing Its History

Amyotrophic lateral sclerosis: A 40-year personal perspective

Transcranial magnetic stimulation and amyotrophic lateral sclerosis: pathophysiological insights

A proposal for new diagnostic criteria for ALS

Amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis: Origins traced to impaired balance between neural excitation and inhibition in the neonatal period

The strength of corticomotoneuronal drive underlies ALS split phenotypes and reflects early upper motor neuron dysfunction

Neuronal network disintegration: common pathways linking neurodegenerative diseases

ALS/FTD: Evolution, Aging, and Cellular Metabolic Exhaustion

History of ALS and the competing theories on pathogenesis: IFCN handbook chapter

In Memorium: Jun Kimura, MD

Serum MicroRNAs Reflect Injury Severity in a Large Animal Model of Thoracic Spinal Cord Injury

The relationship between personality disorder traits, emotional intelligence, and college adjustment

Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p

Abstract 4127: RX-5902 exhibits direct and immunomodulatory anti-tumor activities in melanoma PDX models

RX-5902, a novel β-catenin modulator, potentiates the efficacy of immune checkpoint inhibitors in preclinical models of triple-negative breast Cancer

Central nervous system in motor neuron disease

The split hand syndrome in amyotrophic lateral sclerosis

Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis

The motor deficit of ALS reflects failure to generate muscle synergies for complex motor tasks, not just muscle strength

Nanoplastics and Neurodegeneration in ALS

Hypothesis: amyotrophic lateral sclerosis and environmental pollutants

The impact of respite care from the perspectives and experiences of people with amyotrophic lateral sclerosis and their care partners: a qualitative study

The motor cortex and amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis-Evolutionary and other perspectives

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