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Brain Sciences|July 2, 2021
Informal Caregiving in Amyotrophic Lateral Sclerosis (ALS): A High Caregiver Burden and Drastic Consequences on Caregivers' LivesPavel Schischlevskij, Isabell Cordts, René Günther, et al.
Molecular Metabolism|April 2, 2021
Compound- and fiber type-selective requirement of AMPKγ3 for insulin-independent glucose uptake in skeletal musclePhilipp Rhein, Eric M Desjardins, Ping Rong, et al.
Brain Sciences|April 3, 2021
A Nation-Wide, Multi-Center Study on the Quality of Life of ALS Patients in GermanyTara Peseschkian, Isabell Cordts, René Günther, et al.
Nature Communications|August 8, 2018
SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defectsJohanne Dubail, Céline Huber, Sandrine Chantepie, et al.
Environmental Research|November 14, 1997
The assessment of biomarkers to detect nephrotoxicity using an integrated databaseS A Taylor, I D Chivers, R G Price, et al.
Journal of Neurology|June 25, 2023
Economic evaluation of Motor Neuron Diseases: a nationwide cross-sectional analysis in GermanyFelix Heinrich, Isabell Cordts, René Günther, et al.
Physical Review Letters|January 7, 2021
High-Precision Determination of Oxygen K_{α} Transition Energy Excludes Incongruent Motion of Interstellar OxygenM A Leutenegger, S Kühn, P Micke, et al.
The Lancet. Neurology|March 22, 2020
Nusinersen in adults with 5q spinal muscular atrophy: a non-interventional, multicentre, observational cohort studyTim Hagenacker, Claudia D Wurster, René Günther, et al.
Neurogenetics|August 27, 2017
X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1Noriko Miyake, Nicole I Wolf, Ferdy K Cayami, et al.
Scientific Reports|March 27, 2020
Selective USP7 inhibition elicits cancer cell killing through a p53-dependent mechanismNathan J Schauer, Xiaoxi Liu, Robert S Magin, et al.
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