Publikationen der ALS-Forschungsgruppe an der Charité
Neurofilament light chain (NfL) – Biomarker für die ALS-Progression
Meyer T, Salkic E, Grehl T, Weyen U, Kettemann D, Weydt P,
Der Einsatz von Patient-reported Outcome Measures (PROM) und die Perspektive digitaler Biomarker bei der Amyotrophen Lateralsklerose
Maier A, Münch C, Meyer T. Klinische Neurophysiologie 2023; 54(01): 28-34. doi:
Acceptance of Enhanced Robotic Assistance Systems in People With Amyotrophic Lateral Sclerosis-Associated Motor Impairment: Observational Online Study
Maier A, Eicher C, Kiselev J, Klebbe R, Greuèl M, Kettemann D,
Remote digital assessment of amyotrophic lateral sclerosis functional rating scale – a multicenter observational study
Meyer T, Spittel S, Grehl T, Weyen U, Steinbach R, Kettemann D,
Use and subjective experience of the impact of motor-assisted movement exercisers in people with amyotrophic lateral sclerosis: a multicenter observational study
Maier A, Gaudlitz M, Grehl T, Weyen U, Steinbach R, Grosskreutz J,
Non-invasive and tracheostomy invasive ventilation in amyotrophic lateral sclerosis: Utilization and survival rates in a cohort study over 12 years in Germany
Spittel S, Maier A, Kettemann D, Walter B, Koch B, Krause K,
Publikationen mit Beteiligung der ALS-Forschungsgruppe an der Charité
PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis
Eschbach J, Schwalenstöcker B, Soyal SM,
Optical coherence tomography does not support optic nerve involvement in amyotrophic lateral sclerosis
Roth NM, Saidha S, Zimmermann H,
The dynactin p150 subunit: cell biology studies of sequence changes found in ALS/MND and Parkinsonian syndromes
Stockmann M, Meyer-Ohlendorf M, Achberger K,
NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis
Blauw HM, van Rheenen W, Koppers
Ataxin-2 intermediate-length polyglutamine expansions in European ALS patients
Lee T, Li YR, Ingre C,
A large genome scan for rare CNVs in amyotrophic lateral sclerosis
Blauw HM, Al-Chalabi A, Andersen PM,
Novel missense and truncating mutations in FUS/TLS in familial ALS
Waibel S, Neumann M, Rabe M,
No evidence of association of FLJ10986 and ITPR2 with ALS in a large German cohort
Fernández-Santiago R, Sharma M, Berg D,
