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Ueda, Sakiho
9  Ergebnisse:
Personensuche X
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1

Acute inhibition of AMPA receptors by perampanel reduces am..:

Ueda, Sakiho ; Kuzuya, Akira ; Kawata, Masayoshi...
The FASEB Journal.  37 (2023)  11 - p. , 2023
Link: https://doi.org/10.1096/..
 
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2

Thigh muscle MRI findings in myopathy associated with anti‐..:

Minamiyama, Sumio ; Ueda, Sakiho ; Nakashima, Ran...
Muscle & Nerve.  61 (2019)  1 - p. 81-87 , 2019
Link: https://doi.org/10.1002/..
 
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3

Nivolumab causes focal muscular inflammation without electr..:

Li, Fangzhou ; Ayaki, Takashi ; Ueda, Sakiho...
Neurology and Clinical Neuroscience.  6 (2018)  4 - p. 112-114 , 2018
Link: https://doi.org/10.1111/..
 
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4

Degradation of amyloid β peptide by neprilysin expressed fr..:

Sakai, Madoka ; Ueda, Sakiho ; Daito, Takuji...
Microbiology and Immunology.  62 (2018)  7 - p. 467-472 , 2018
Link: https://doi.org/10.1111/..
 
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5

Benign adult familial myoclonus epilepsy is a progressive d..:

Hitomi, Takefumi ; Kobayashi, Katsuya ; Sakurai, Takeyo...
Epileptic Disorders.  18 (2016)  1 - p. 67-72 , 2016
Link: https://doi.org/10.1684/..
 
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6

A novel A792D mutation in the CSF1R gene causes hereditary ..:

Ueda, Sakiho ; Yamashita, Hirofumi ; Hikiami, Ryota...
eNeurologicalSci.  1 (2015)  1 - p. 7-9 , 2015
Link: https://doi.org/10.1016/..
 
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7

Acute inhibition of AMPA receptors by perampanel reduces am..:

Ueda, Sakiho ; Kuzuya, Akira ; Kawata, Masayoshi...
10.1096/fj.202300837R.  , 2023
Link: http://hdl.handle.net/24..
 
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8

A novel A792D mutation in the CSF1R gene causes hereditary ..:

Ueda, Sakiho ; Yamashita, Hirofumi ; Hikiami, Ryota...
10.1016/j.ensci.2015.07.001.  , 2015
Link: http://hdl.handle.net/24..
 
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9

A novel A792D mutation in the CSF1R gene causes hereditary ..:

Sakiho Ueda ; Hirofumi Yamashita ; Ryota Hikiami...
http://www.sciencedirect.com/science/article/pii/S2405650215000040.  , 2015
Link: https://doi.org/10.1016/..
 
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