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

Nature communications, 2018-01, Vol.9 (1), p.335-17, Article 335

2018

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Cognitive performance of adult patients with SMA before and after treatment initiation with nusinersen

BMC neurology, 2023-06, Vol.23 (1), p.216-216, Article 216

2023

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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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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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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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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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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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Affection of Respiratory Muscles in ALS and SMA

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

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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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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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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Patients’ and caregivers’ perception of multidimensional and palliative care in amyotrophic lateral sclerosis – protocol of a German multicentre study

Neurological research and practice, 2024-07, Vol.6 (1), p.34-8, Article 34

2024

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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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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

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

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

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

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

Cognitive performance of adult patients with SMA before and after treatment initiation with nusinersen

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

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

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

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

Non-Motor Symptoms in Patients Suffering from Motor Neuron Diseases

Affection of Respiratory Muscles in ALS and SMA

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

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

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

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

Patients’ and caregivers’ perception of multidimensional and palliative care in amyotrophic lateral sclerosis – protocol of a German multicentre study

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

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

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