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Now showing items 11-20 of 34
FXN GAA repeat expansions in amyotrophic lateral sclerosis
Rizik, Naji et al. (2014)
Wissenschaftlicher Artikel
NOVEL ETFDH MUTATION AND IMAGING FINDINGS IN AN ADULT WITH GLUTARIC ACIDURIA TYPE II
Rosenbohm, Angela et al. (2014)
Wissenschaftlicher Artikel
Impact of the control for corrupted diffusion tensor imaging data in comparisons at the group level: an application in Huntington disease
Müller, Hans-Peter et al. (2014)
Wissenschaftlicher Artikel
Davunetide in patients with progressive supranuclear palsy: a randomised, double-blind, placebo-controlled phase 2/3 trial
Boxer, Adam L. et al. (2014)
Wissenschaftlicher Artikel
Live and let die: existential decision processes in a fatal disease
Lule, Dorothee et al. (2014)
Wissenschaftlicher Artikel
Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease
Mueller, Kathrin et al. (2014)
Wissenschaftlicher Artikel
Additional resources and the default mode network: Evidence of increased connectivity and decreased white matter integrity in amyotrophic lateral sclerosis
Heimrath, Johana et al. (2014)
Wissenschaftlicher Artikel
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study
Van Doormaal, Perry T. C. et al. (2014)
Wissenschaftlicher Artikel
Two-Point Magnitude MRI for Rapid Mapping of Brown Adipose Tissue and Its Application to the R6/2 Mouse Model of Huntington Disease
Lindenberg, Katrin S. et al. (2014)
Wissenschaftlicher Artikel
Phosphoinositide 3-Kinases Upregulate System x(c)(-) via Eukaryotic Initiation Factor 2 alpha and Activating Transcription Factor 4-A Pathway Active in Glioblastomas and Epilepsy
Lewerenz, Jan et al. (2014)
Wissenschaftlicher Artikel