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
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,
