Transcranial Magnetic Stimulation with the Maximum Voluntary Muscle Contraction Facilitates Motor Neuron Excitability and Muscle Force

por Touge, Tetsuo, Urai, Yoshiteru, Ikeda, Kazuyo, Kume, Kodai, Deguchi, Kazushi
Publicado 2012

Acute Intermittent Porphyria Presenting with Posterior Reversible Encephalopathy Syndrome, Accompanied by Prolonged Vasoconstriction

por Takata, Tadayuki, Kume, Kodai, Kokudo, Yohei, Ikeda, Kazuyo, Kamada, Masaki, Touge, Tetsuo, Deguchi, Kazushi, Masaki, Tsutomu
Publicado 2017

Subacute Sensorimotor Neuropathy Accompanied by Anti-ganglioside GM1 Antibody in a Patient with Lung Cancer

por Kanaji, Nobuhiro, Kume, Kodai, Mizoguchi, Hitoshi, Inoue, Takuya, Watanabe, Naoki, Nishiyama, Noriko, Kadowaki, Norimitsu, Ishii, Tomoya
Publicado 2018

Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report

por Kume, Kodai, Morino, Hiroyuki, Miyamoto, Ryosuke, Matsuda, Yukiko, Ohsawa, Ryosuke, Kanaya, Yuhei, Tada, Yui, Kurashige, Takashi, Kawakami, Hideshi
Publicado 2020

Three cases of non-carryover fingolimod-PML: Is the risk in Japan increased?

por Nakahara, Jin, Tomaske, Laura, Kume, Kodai, Takata, Tadayuki, Kamada, Masaki, Deguchi, Kazushi, Kufukihara, Kenji, Schneider, Ruth, Gold, Ralf, Ayzenberg, Ilya
Publicado 2019

Premedication of hemin for eradication therapy of Helicobacter pylori in patients with porphyria

por Takata, Tadayuki, Kokudo, Yohei, Morishita, Asahiro, Kume, Kodai, Yachida, Tatsuo, Kamada, Masaki, Kobara, Hideki, Deguchi, Kazushi, Touge, Tetsuo, Masugata, Hisashi, Masaki, Tsutomu
Publicado 2020

FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report

por Toko, Megumi, Ohshita, Tomohiko, Kurashige, Takashi, Morino, Hiroyuki, Kume, Kodai, Yamashita, Hiroshi, Sobue, Gen, Iwasaki, Yasushi, Sone, Jun, Kawakami, Hideshi, Maruyama, Hirofumi
Publicado 2021

Correction to: FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report

por Toko, Megumi, Ohshita, Tomohiko, Kurashige, Takashi, Morino, Hiroyuki, Kume, Kodai, Yamashita, Hiroshi, Sobue, Gen, Iwasaki, Yasushi, Sone, Jun, Kawakami, Hideshi, Maruyama, Hirofumi
Publicado 2021

Serum microRNA expression profiling in patients with multiple system atrophy

por Kume, Kodai, Iwama, Hisakazu, Deguchi, Kazushi, Ikeda, Kazuyo, Takata, Tadayuki, Kokudo, Yohei, Kamada, Masaki, Fujikawa, Keiko, Hirose, Kayo, Masugata, Hisashi, Touge, Tetsuo, Masaki, Tsutomu
Publicado 2018

Biallelic mutation of HSD17B4 induces middle age–onset spinocerebellar ataxia

por Matsuda, Yukiko, Morino, Hiroyuki, Miyamoto, Ryosuke, Kurashige, Takashi, Kume, Kodai, Mizuno, Noriyoshi, Kanaya, Yuhei, Tada, Yui, Ohsawa, Ryosuke, Yokota, Kazunori, Shimozawa, Nobuyuki, Maruyama, Hirofumi, Kawakami, Hideshi
Publicado 2020

‘Raisin bread sign’ feature of pontine autosomal dominant microangiopathy and leukoencephalopathy

por Kikumoto, Mai, Kurashige, Takashi, Ohshita, Tomohiko, Kume, Kodai, Kikumoto, Osamu, Nezu, Tomohisa, Aoki, Shiro, Ochi, Kazuhide, Morino, Hiroyuki, Nomura, Eiichi, Yamashita, Hiroshi, Kaneko, Mayumi, Maruyama, Hirofumi, Kawakami, Hideshi
Publicado 2023

Spinocerebellar ataxia type 17-digenic TBP/STUB1 disease: neuropathologic features of an autopsied patient

por Saito, Rie, Tada, Yui, Oikawa, Daisuke, Sato, Yusuke, Seto, Makiko, Satoh, Akira, Kume, Kodai, Ueki, Nozomi, Nakashima, Masahiro, Hayashi, Shintaro, Toyoshima, Yasuko, Tokunaga, Fuminori, Kawakami, Hideshi, Kakita, Akiyoshi
Publicado 2022

Co-morbidity of progressive supranuclear palsy and amyotrophic lateral sclerosis: a clinical-pathological case report

por Fujita, Koji, Matsubara, Tomoyasu, Miyamoto, Ryosuke, Sumikura, Hiroyuki, Takeuchi, Toshiaki, Maruyama Saladini, Keiko, Kawarai, Toshitaka, Nodera, Hiroyuki, Udaka, Fukashi, Kume, Kodai, Morino, Hiroyuki, Kawakami, Hideshi, Hasegawa, Masato, Kaji, Ryuji, Murayama, Shigeo, Izumi, Yuishin
Publicado 2019