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Glial fibrillary acidic protein as blood biomarker for differential diagnosis and severity of major depressive disorder
Steinacker, Petra et al. (2021)
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Existential decision-making in a fatal progressive disease: how much do legal and medical frameworks matter?
Weber, Christian et al. (2017)
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Altered perivascular fibroblast activity precedes ALS disease onset
Manberg, Anna et al. (2021)
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Accelerated aging phenotype in mice with conditional deficiency for mitochondrial superoxide dismutase in the connective tissue
Treiber, Nicolai et al. (2011)
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Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia
Freischmidt, Axel et al. (2015)
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Super-Resolution Microscopy Reveals Presynaptic Localization of the ALS/FTD Related Protein FUS in Hippocampal Neurons
Schoen, Michael et al. (2016)
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The role of de novo mutations in the development of amyotrophic lateral sclerosis
van Doormaal, Perry T. C. et al. (2017)
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Neurofilament light and heterogeneity of disease progression in amyotrophic lateral sclerosis: development and validation
of a prediction model to improve interventional trials
Witzel, Simon et al. (2021)
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ALS-causing mutations differentially affect PGC-1 alpha expression and function in the brain vs. peripheral tissues
Bayer, Hanna et al. (2017)
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Increased chitotriosidase 1 concentration following nusinersen treatment in spinal muscular atrophy
Freigang, Maren et al. (2021)
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