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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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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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Motor Unit Number Index (MUNIX) of hand muscles is a disease biomarker for adult spinal muscular atrophy

Clinical neurophysiology, 2019-02, Vol.130 (2), p.315-319

2019

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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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Neurofilament light chain in serum of adolescent and adult SMA patients under treatment with nusinersen

Journal of neurology, 2020, Vol.267 (1), p.36-44

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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Increased chitotriosidase 1 concentration following nusinersen treatment in spinal muscular atrophy

Orphanet journal of rare diseases, 2021-07, Vol.16 (1), p.330-330, Article 330

2021

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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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Macrophage inclusions in cerebrospinal fluid following treatment initiation with antisense oligonucleotide therapies in motor neuron diseases

Neurological research and practice, 2024-02, Vol.6 (1), p.11-11, Article 11

2024

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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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Affection of Respiratory Muscles in ALS and SMA

Journal of clinical medicine, 2022-02, Vol.11 (5), p.1163

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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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

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)

Motor Unit Number Index (MUNIX) of hand muscles is a disease biomarker for adult spinal muscular atrophy

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

Neurofilament light chain in serum of adolescent and adult SMA patients under treatment with nusinersen

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

Increased chitotriosidase 1 concentration following nusinersen treatment in spinal muscular atrophy

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

Macrophage inclusions in cerebrospinal fluid following treatment initiation with antisense oligonucleotide therapies in motor neuron diseases

Non-Motor Symptoms in Patients Suffering from Motor Neuron Diseases

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

Affection of Respiratory Muscles in ALS and SMA

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

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

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