Area of research
Genetics · Neurology
Research interest
Research interests include Medicine, Amyotrophic lateral sclerosis, Spinal muscular atrophy, SMA*, Quality of life (healthcare), and Observational study.
Respiratory function in 192 adult patients with spinal muscular atrophy (SMA) treated with nusinersen – a multicenter observational study
Serglycin und Periostin als potenzielle neue Serum-Biomarker für die GNE-Myopathie
Long-term efficacy and safety of nusinersen in adults with 5q spinal muscular atrophy: a prospective European multinational observational study
Risdiplam therapy in adults with 5q-SMA: observational study on motor function and treatment satisfaction
Economic evaluation of Motor Neuron Diseases: a nationwide cross-sectional analysis in Germany
Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Treatment expectations and perception of therapy in adult patients with spinal muscular atrophy receiving nusinersen
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
A Nation-Wide, Multi-Center Study on the Quality of Life of ALS Patients in Germany
Nusinersen in adults with 5q spinal muscular atrophy: a non-interventional, multicentre, observational cohort study
Treatment expectations and patient-reported outcomes of nusinersen therapy in adult spinal muscular atrophy
Impact of comorbidities and co-medication on disease onset and progression in a large German ALS patient group
Costs of illness in amyotrophic lateral sclerosis (ALS): a cross-sectional survey in Germany
An observational cohort study on impact, dimensions and outcome of perceived fatigue in adult 5q-spinal muscular atrophy patients receiving nusinersen treatment
Neurofilament light chain in serum of adolescent and adult SMA patients under treatment with nusinersen
Safety and efficacy of rasagiline as an add-on therapy to riluzole in patients with amyotrophic lateral sclerosis: a randomised, double-blind, parallel-group, placebo-controlled, phase 2 trial
FIG4 variants in central European patients with amyotrophic lateral sclerosis: a whole-exome and targeted sequencing study
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