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Jan Wagner

Showing results (51-60 of 55) with videos related to

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Brain : a Journal of Neurology|January 25, 2018
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA studyChristopher D Whelan, Andre Altmann, Juan A Botía, et al.
Neuropathology and Applied Neurobiology|August 13, 2021
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsiesAndre Altmann, Mina Ryten, Martina Di Nunzio, et al.
Nature|April 26, 2023
A ring-like accretion structure in M87 connecting its black hole and jetRu-Sen Lu, Keiichi Asada, Thomas P Krichbaum, et al.
Physical Review Letters|October 16, 2020
Gravitational Test beyond the First Post-Newtonian Order with the Shadow of the M87 Black HoleDimitrios Psaltis, Lia Medeiros, Pierre Christian, et al.
Nature Genetics|March 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
Brain : a Journal of Neurology|January 25, 2018
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA studyChristopher D Whelan, Andre Altmann, Juan A Botía, et al.
Neuropathology and Applied Neurobiology|August 13, 2021
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsiesAndre Altmann, Mina Ryten, Martina Di Nunzio, et al.
Nature|April 26, 2023
A ring-like accretion structure in M87 connecting its black hole and jetRu-Sen Lu, Keiichi Asada, Thomas P Krichbaum, et al.
Physical Review Letters|October 16, 2020
Gravitational Test beyond the First Post-Newtonian Order with the Shadow of the M87 Black HoleDimitrios Psaltis, Lia Medeiros, Pierre Christian, et al.
Nature Genetics|March 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.
Pageof 6