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FUS Is Not Mislocalized in Spinal Motor Neurons Derived From Human Induced Pluripotent Stem Cells of Main Non-FUS ALS Subtypes

Journal of neuropathology and experimental neurology, 2021-07, Vol.80 (7), p.720-722

2021

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Rho kinase inhibition modulates microglia activation and improves survival in a model of amyotrophic lateral sclerosis

Glia, 2014-02, Vol.62 (2), p.217-232

2014

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ROCK-ALS: Protocol for a Randomized, Placebo-Controlled, Double-Blind Phase IIa Trial of Safety, Tolerability and Efficacy of the Rho Kinase (ROCK) Inhibitor Fasudil in Amyotrophic Lateral Sclerosis

Frontiers in neurology, 2019-03, Vol.10, p.293

2019

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Use and subjective experience of the impact of motor-assisted movement exercisers in people with amyotrophic lateral sclerosis: a multicenter observational study

Scientific reports, 2022-06, Vol.12 (1), p.9657-9657, Article 9657

2022

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Impairment in Respiratory Function Contributes to Olfactory Impairment in Amyotrophic Lateral Sclerosis

Frontiers in neurology, 2018-02, Vol.9, p.79-79

2018

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Interleukin-17 and Th17 Lymphocytes Directly Impair Motoneuron Survival of Wildtype and FUS-ALS Mutant Human iPSCs

International journal of molecular sciences, 2021-08, Vol.22 (15), p.8042

2021

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Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis

Annals of clinical and translational neurology, 2019-12, Vol.6 (12), p.2384-2394

2019

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One nerve suffices: A clinically guided nerve ultrasound protocol for the differentiation of multifocal motor neuropathy (MMN) and amyotrophic lateral sclerosis (ALS)

Journal of neurology, 2021-04, Vol.268 (4), p.1495-1507

2021

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AMYOTROPHIC LATERAL SCLEROSIS SELECTIVE CORTICOSPINAL TRACT MYELIN IMAGING AND DIFFUSION MRI

Clinical neuroradiology (Munich), 2019-09, Vol.29 (S1), p.S33

2019

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Peripheral proinflammatory Th1/Th17 immune cell shift is linked to disease severity in amyotrophic lateral sclerosis

Scientific reports, 2020-04, Vol.10 (1), p.5941-5941, Article 5941

2020

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FUS ALS neurons activate major stress pathways and reduce translation as an early protective mechanism against neurodegeneration

Cell reports (Cambridge), 2023-02, Vol.42 (2), p.112025-112025, Article 112025

2023

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Human Spinal Motor Neurons Are Particularly Vulnerable to Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis Patients

International journal of molecular sciences, 2020-05, Vol.21 (10), p.3564

2020

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Caregivers' View of Socio-Medical Care in the Terminal Phase of Amyotrophic Lateral Sclerosis-How Can We Improve Holistic Care in ALS?

Journal of clinical medicine, 2022-01, Vol.11 (1), p.254

2022

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Non-Motor Symptoms in Patients Suffering from Motor Neuron Diseases

Frontiers in neurology, 2016-07, Vol.7, p.117-117

2016

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Serum creatine kinase and creatinine in adult spinal muscular atrophy under nusinersen treatment

Annals of clinical and translational neurology, 2021-05, Vol.8 (5), p.1049-1063

2021

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Alteration of Mitochondrial Integrity as Upstream Event in the Pathophysiology of SOD1-ALS

Cells (Basel, Switzerland), 2022-04, Vol.11 (7), p.1246

2022

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ALSFRS-R-SE: an adapted, annotated, and self-explanatory version of the revised amyotrophic lateral sclerosis functional rating scale

Neurological research and practice, 2022-12, Vol.4 (1), p.60-60, Article 60

2022

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Validity and reliability of the German multidimensional fatigue inventory in spinal muscular atrophy

Annals of clinical and translational neurology, 2022-03, Vol.9 (3), p.351-362

2022

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The palmomental reflex in amyotrophic lateral sclerosis - a clinical sign of executive or motor dysfunction?

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2021-10, Vol.22 (7-8), p.1-591

2021

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Impairment of oculomotor functions in patients with early to advanced amyotrophic lateral sclerosis

Journal of neurology, 2024, Vol.271 (1), p.325-339

2024

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Quality of life and mental health in the locked-in-state—differences between patients with amyotrophic lateral sclerosis and their next of kin

Journal of neurology, 2022-11, Vol.269 (11), p.5910-5925

2022

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FUS Is Not Mislocalized in Spinal Motor Neurons Derived From Human Induced Pluripotent Stem Cells of Main Non-FUS ALS Subtypes

Rho kinase inhibition modulates microglia activation and improves survival in a model of amyotrophic lateral sclerosis

ROCK-ALS: Protocol for a Randomized, Placebo-Controlled, Double-Blind Phase IIa Trial of Safety, Tolerability and Efficacy of the Rho Kinase (ROCK) Inhibitor Fasudil in Amyotrophic Lateral Sclerosis

Use and subjective experience of the impact of motor-assisted movement exercisers in people with amyotrophic lateral sclerosis: a multicenter observational study

Impairment in Respiratory Function Contributes to Olfactory Impairment in Amyotrophic Lateral Sclerosis

Interleukin-17 and Th17 Lymphocytes Directly Impair Motoneuron Survival of Wildtype and FUS-ALS Mutant Human iPSCs

Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis

One nerve suffices: A clinically guided nerve ultrasound protocol for the differentiation of multifocal motor neuropathy (MMN) and amyotrophic lateral sclerosis (ALS)

AMYOTROPHIC LATERAL SCLEROSIS SELECTIVE CORTICOSPINAL TRACT MYELIN IMAGING AND DIFFUSION MRI

Peripheral proinflammatory Th1/Th17 immune cell shift is linked to disease severity in amyotrophic lateral sclerosis

Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation

FUS ALS neurons activate major stress pathways and reduce translation as an early protective mechanism against neurodegeneration

Human Spinal Motor Neurons Are Particularly Vulnerable to Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis Patients

Caregivers' View of Socio-Medical Care in the Terminal Phase of Amyotrophic Lateral Sclerosis-How Can We Improve Holistic Care in ALS?

Non-Motor Symptoms in Patients Suffering from Motor Neuron Diseases

Serum creatine kinase and creatinine in adult spinal muscular atrophy under nusinersen treatment

Informal Caregiving in Amyotrophic Lateral Sclerosis (ALS): A High Caregiver Burden and Drastic Consequences on Caregivers’ Lives

Alteration of Mitochondrial Integrity as Upstream Event in the Pathophysiology of SOD1-ALS

ALSFRS-R-SE: an adapted, annotated, and self-explanatory version of the revised amyotrophic lateral sclerosis functional rating scale

A Nation-Wide, Multi-Center Study on the Quality of Life of ALS Patients in Germany

Validity and reliability of the German multidimensional fatigue inventory in spinal muscular atrophy

Safety and Effectiveness of Long-term Intravenous Administration of Edaravone for Treatment of Patients With Amyotrophic Lateral Sclerosis

The palmomental reflex in amyotrophic lateral sclerosis - a clinical sign of executive or motor dysfunction?

Impairment of oculomotor functions in patients with early to advanced amyotrophic lateral sclerosis

Quality of life and mental health in the locked-in-state—differences between patients with amyotrophic lateral sclerosis and their next of kin

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