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Internal Medicine (Tokyo, Japan)|September 14, 2022
Spinocerebellar Ataxia Type 31 Exacerbated by Anti-amino Terminal of Alpha-enolase AutoantibodiesSatoshi Zeniya, Nobuo Sanjo, Hiroya Kuwahara, et al.Neurobiology of Aging|November 22, 2005
Transient abundance of presenilin 1 fragments/nicastrin complex associated with synaptogenesis during development in rat cerebellumToshiki Uchihara, Nobuo Sanjo, Ayako Nakamura, et al.Frontiers in Neurology|March 6, 2026
Quantitative evaluation of iron chelator effects on central motor and sensory tracts in superficial siderosisRyo Iwase, Nobuo Sanjo, Tadashi Kanouchi, et al.Internal Medicine (Tokyo, Japan)|November 9, 2020
Early Pathological JC Virus Lesions in a Patient without Any MRI-based IndicationsNobuo Sanjo, Yurie Nose, Shouhei Miyamoto, et al.Internal Medicine (Tokyo, Japan)|December 23, 2017
Myasthenia Gravis Complicated with Peripheral T-cell Lymphoma, Not Otherwise Specified (PTCL-NOS), Following Thymectomy and Longstanding Tacrolimus TherapyMasahiro Ohara, Kokoro Ozaki, Takuya Ohkubo, et al.Journal of Affective Disorders|March 10, 2017
Depressive disorder may be associated with raphe nuclei lesions in patients with brainstem infarctionYoshiyuki Numasawa, Takaaki Hattori, Sumio Ishiai, et al.Biomolecules|January 25, 2025
Neurofilament Light Chain Levels in Serum and Cerebrospinal Fluid Do Not Correlate with Survival Times in Patients with Prion DiseaseMika Shimamura, Kong Weijie, Toshiaki Nonaka, et al.Chembiochem : a European Journal of Chemical Biology|April 24, 2026
Rational Design of a Multivalent RNA Combining Structural Motifs Tailored to Multiple Domains of Fused in Sarcoma for Potent Inhibition of AggregationNobuaki Kuroiwa, Fumika Sakaue, Motoki Miura, et al.Internal Medicine (Tokyo, Japan)|June 16, 2016
Progressive Multifocal Leukoencephalopathy with Balanced CD4/CD8 T-Cell Infiltration and Good Response to Mefloquine TreatmentNobuo Sanjo, Satoko Kina, Yukiko Shishido-Hara, et al.Biochemical and Biophysical Research Communications|February 1, 2018
Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein geneYoko Ito, Nobuo Sanjo, Masaki Hizume, et al.Pageof 9