Showing results (401-410 of 528) with videos related to
Sort By:
Pageof 53
Angiogenesis|July 28, 2022
Somatic GJA4 gain-of-function mutation in orbital cavernous venous malformationsHiroki Hongo, Satoru Miyawaki, Yu Teranishi, et al.Geriatrics & Gerontology International|August 5, 2017
Association of subclinical carotid atherosclerosis with immediate memory and other cognitive functionsLumine Matsumoto, Kazushi Suzuki, Yoshiko Mizuno, et al.Scientific Reports|March 27, 2021
Associations of pathological diagnosis and genetic abnormalities in meningiomas with the embryological origins of the meningesAtsushi Okano, Satoru Miyawaki, Hiroki Hongo, et al.Human Mutation|June 3, 2020
Clinical and molecular genetic characterization of two female patients harboring the Xq27.3q28 deletion with different ratios of X chromosome inactivationKimiko Katoh, Kaori Aiba, Daisuke Fukushi, et al.Journal of Human Genetics|April 22, 2025
Elevated serum autotaxin levels and multiple system atrophy-like presentation in a patient with PLA2G6-associated neurodegenerationSo Okubo, Takashi Matsukawa, Norifumi Kawamoto, et al.Brain Research|June 18, 2018
Methylation changes and aberrant expression of FGFR3 in Lewy body disease neuronsTakeyuki Tsuchida, Tatsuo Mano, Kagari Koshi-Mano, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 1, 2013
Recurrent K3E mutation in Cu/Zn superoxide dismutase gene associated with amyotrophic lateral sclerosisMagdalena Kuźma-Kozakiewicz, Mariusz Berdyński, Mitsuya Morita, et al.Clinical Neurology and Neurosurgery|December 8, 2009
Efferent and afferent evoked potentials in patients with adrenomyeloneuropathyHideyuki Matsumoto, Ritsuko Hanajima, Yasuo Terao, et al.Journal of Atherosclerosis and Thrombosis|March 27, 2024
Genetic and Functional Analyses of Patients with Marked Hypo-High-Density Lipoprotein CholesterolemiaYasuhisa Furuta, Yoshinori Osaki, Yoshimi Nakagawa, et al.Journal of Neurophysiology|August 28, 2015
Modulation of error-sensitivity during a prism adaptation task in people with cerebellar degenerationRitsuko Hanajima, Reza Shadmehr, Shinya Ohminami, et al.Pageof 53