Search
Now showing items 31-35 of 35
A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany
Weishaupt, Jochen H. et al. (2013)
Wissenschaftlicher Artikel
Truncating mutations in FUS/TLS give rise to a more aggressive ALS-phenotype than missense mutations: a clinico-genetic study in Germany
Waibel, Stefan et al. (2013)
Wissenschaftlicher Artikel
H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis
van Rheenen, Wouter et al. (2013)
Wissenschaftlicher Artikel
Mechanisms, models and biomarkers in amyotrophic lateral sclerosis
Turner, Martin R. et al. (2013)
Wissenschaftlicher Artikel
Peer recommendations on how to improve clinical research, and Conference wrap-up
Chad, David A. et al. (2013)
Wissenschaftlicher Artikel