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Plos One|August 22, 2014
Two-point magnitude MRI for rapid mapping of brown adipose tissue and its application to the R6/2 mouse model of Huntington diseaseKatrin S Lindenberg, Patrick Weydt, Hans-Peter Müller, et al.The American Journal of Clinical Nutrition|December 12, 2019
The role of the gut microbiome in the association between habitual anthocyanin intake and visceral abdominal fat in population-level analysisAmy Jennings, Manja Koch, Majken K Jensen, et al.Journal of Neurology|February 19, 2014
Do eye movement impairments in patients with small vessel cerebrovascular disease depend on lesion load or on cognitive deficits? A video-oculographic and MRI studyElmar H Pinkhardt, Hazem Issa, Martin Gorges, et al.Translational Neurodegeneration|June 1, 2021
Disruption of orbitofrontal-hypothalamic projections in a murine ALS model and in human patientsDavid Bayer, Stefano Antonucci, Hans-Peter Müller, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 10, 2016
A large-scale multicentre cerebral diffusion tensor imaging study in amyotrophic lateral sclerosisHans-Peter Müller, Martin R Turner, Julian Grosskreutz, et al.Plos One|November 13, 2015
Eye Movement Deficits Are Consistent with a Staging Model of pTDP-43 Pathology in Amyotrophic Lateral SclerosisMartin Gorges, Hans-Peter Müller, Dorothée Lulé, et al.Annals of Clinical and Translational Neurology|December 3, 2019
Severe white matter damage in SHANK3 deficiency: a human and translational studySarah Jesse, Hans-Peter Müller, Michael Schoen, et al.European Journal of Nutrition|February 16, 2018
Dietary pattern associated with selenoprotein P and MRI-derived body fat volumes, liver signal intensity, and metabolic disordersRomina di Giuseppe, Sandra Plachta-Danielzik, Manja Koch, et al.Biomedicines|August 26, 2022
Association of Serum GFAP with Functional and Neurocognitive Outcome in Sporadic Small Vessel DiseaseAndré Huss, Ahmed Abdelhak, Benjamin Mayer, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 29, 2020
Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers-a developmental disorderDorothée E Lulé, Hans-Peter Müller, Julia Finsel, et al.Pageof 19