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Neuropathology : Official Journal of the Japanese Society of Neuropathology|January 14, 2012
Fatal subarachnoid hemorrhage caused by Aspergillus arteritis without angiographic abnormalitiesYasuo Miki, Masahiko Tomiyama, Rie Haga, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|June 23, 2015
Localization of nuclear receptor subfamily 4, group A, member 3 (NR4A3) in Lewy body disease and multiple system atrophyTomoya Kon, Yasuo Miki, Kunikazu Tanji, et al.
Journal of Neuropathology and Experimental Neurology|March 16, 2022
Accumulation of Nonfibrillar TDP-43 in the Rough Endoplasmic Reticulum Is the Early-Stage Pathology in Amyotrophic Lateral SclerosisTomoya Kon, Fumiaki Mori, Kunikazu Tanji, et al.
NPJ Parkinson'S Disease|December 7, 2023
Development and validation of an expanded antibody toolset that captures alpha-synuclein pathological diversity in Lewy body diseasesMelek Firat Altay, Senthil T Kumar, Johannes Burtscher, et al.
Acta Neuropathologica Communications|May 21, 2015
Filamentous aggregations of phosphorylated α-synuclein in Schwann cells (Schwann cell cytoplasmic inclusions) in multiple system atrophyKeiko Nakamura, Fumiaki Mori, Tomoya Kon, et al.
Brain Pathology (Zurich, Switzerland)|November 22, 2014
p62 Deficiency Enhances α-Synuclein Pathology in MiceKunikazu Tanji, Saori Odagiri, Yasuo Miki, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|September 3, 2015
Accumulation of phosphorylated α-synuclein in subpial and periventricular astrocytes in multiple system atrophy of long durationKeiko Nakamura, Fumiaki Mori, Tomoya Kon, et al.
Journal of Gastrointestinal and Liver Diseases : JGLD|August 25, 2022
Examination of Abnormal Alpha-synuclein Aggregates in the Enteric Neural Plexus in Patients with Ulcerative ColitisNoriaki Gibo, Tomonari Hamaguchi, Yasuo Miki, et al.
Frontiers in Neuroscience|August 12, 2024
Behavioral and histological analyses of the mouse <i>Bassoon</i> p.P3882A mutation corresponding to the human <i>BSN</i> p.P3866A mutationDaiki Tanaka, Hiroaki Yaguchi, Kaichi Yoshizaki, et al.
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