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The Journal of Clinical Investigation|March 2, 2023
CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesisNafisa Nuzhat, Kristof Van Schil, Sandra Liakopoulos, et al.
Human Mutation|July 18, 2017
The role of de novo mutations in the development of amyotrophic lateral sclerosisPerry T C van Doormaal, Nicola Ticozzi, Jochen H Weishaupt, et al.
Neurological Research and Practice|July 3, 2024
Patients' and caregivers' perception of multidimensional and palliative care in amyotrophic lateral sclerosis - protocol of a German multicentre studyKatharina Linse, Constanze Weber, Peter Reilich, et al.
Sensors (Basel, Switzerland)|August 30, 2020
Quantitative Long-Term Monitoring of the Circulating Gases in the KATRIN Experiment Using Raman SpectroscopyMax Aker, Konrad Altenmüller, Armen Beglarian, et al.
Science (New York, N.Y.)|April 10, 2025
Direct neutrino-mass measurement based on 259 days of KATRIN data, Max Aker, Dominic Batzler, et al.
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