Publikationen der ALS-Forschungsgruppe an der Charité
Provision of assistive devices in amyotrophic lateral sclerosis. Analysis of 3 years case management in an internet-based supply network
Funke A, Grehl T, Großkreutz J, Münch C, Walter B, Kettemann D,
Severe loss of appetite in amyotrophic lateral sclerosis patients: online self-assessment study
Holm T, Maier A, Wicks P, Lang D, Linke P, Münch C,
Concomitant amyotrophic lateral sclerosis and paraclinical laboratory features of multiple sclerosis: coincidence or causal relationship?
Borisow N, Meyer T, Paul F. Concomitant amyotrophic lateral sclerosis and paraclinical
Online assessment of ALS functional rating scale compares well to in-clinic evaluation: a prospective trial
Maier A, Holm T, Wicks P, Steinfurth L, Linke P, Münch C,
Motor neuron diseases
Petri S, Meyer T. Motoneuronerkrankungen. Familiäre ALS, SMA, HMN Familial ALS, SMA
Heterozygous S44L missense change of the spastin gene in amyotrophic lateral sclerosis
Münch C, Rolfs A, Meyer T. Heterozygous S44L missense change of the
