Non-traumatic Acute Epidural Hematoma in Multiple Sclerosis Treated With Fingolimod

di Fukai, Ryoko, Takahashi, Keita, Abe, Hiroyuki, Higashiyama, Yuichi, Doi, Hiroshi, Takeuchi, Hideyuki, Tanaka, Fumiaki
Pubblicato in Front Neurol (2019)

Case Report: Anti-MOG Antibody Seroconversion Accompanied by Dimethyl Fumarate Treatment

di Takahashi, Keita, Takeuchi, Hideyuki, Fukai, Ryoko, Nakamura, Haruko, Morihara, Keisuke, Higashiyama, Yuichi, Takahashi, Toshiyuki, Doi, Hiroshi, Tanaka, Fumiaki
Pubblicato in Front Immunol (2021)

Panventriculomegaly with a wide foramen of Magendie and large cisterna magna: clinical, radiological, and genetic analysis

di Kageyama, Hiroshi, Ogino, Ikuko, Shimoji, Kazuaki, Nakajima, Madoka, Fukai, Ryoko, Miyake, Noriko, Nishiyama, Kenichi, Matsumoto, Naomichi, Arai, Hajime, Miyajima, Masakazu
Pubblicato in Fluids Barriers CNS (2015)

Two novel homozygous RAB3GAP1 mutations cause Warburg micro syndrome

di Imagawa, Eri, Fukai, Ryoko, Behnam, Mahdiyeh, Goyal, Manisha, Nouri, Narges, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Saitsu, Hirotomo, Salehi, Mansour, Kapoor, Seema, Tanaka, Fumiaki, Miyake, Noriko, Matsumoto, Naomichi
Pubblicato in Hum Genome Var (2015)

A Case of McLeod Syndrome with A Novel XK Missense Mutation

di Komiya, Hiroyasu, Takasu, Mutsuki, Hashiguchi, Shunta, Uematsu, Eri, Fukai, Ryoko, Tanaka, Kenichi, Tada, Mikiko, Joki, Hideto, Takahashi, Tatsuya, Koyano, Shigeru, Doi, Hiroshi, Takeuchi, Hideyuki, Tanaka, Fumiaki
Pubblicato in Mov Disord Clin Pract (2018)

De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis

di Kanemasa, Hikaru, Fukai, Ryoko, Sakai, Yasunari, Torio, Michiko, Miyake, Noriko, Lee, Sooyoung, Ono, Hiroaki, Akamine, Satoshi, Nishiyama, Kei, Sanefuji, Masafumi, Ishizaki, Yoshito, Torisu, Hiroyuki, Saitsu, Hirotomo, Matsumoto, Naomichi, Hara, Toshiro
Pubblicato in BMC Neurol (2016)

SGTA associates with intracellular aggregates in neurodegenerative diseases

di Kubota, Shun, Doi, Hiroshi, Koyano, Shigeru, Tanaka, Kenichi, Komiya, Hiroyasu, Katsumoto, Atsuko, Ikeda, Shingo, Hashiguchi, Shunta, Nakamura, Haruko, Fukai, Ryoko, Takahashi, Keita, Kunii, Misako, Tada, Mikiko, Takeuchi, Hideyuki, Tanaka, Fumiaki
Pubblicato in Mol Brain (2021)

Cerebrospinal fluid level of Nogo receptor 1 antagonist lateral olfactory tract usher substance (LOTUS) correlates inversely with the extent of neuroinflammation

di Takahashi, Keita, Takeuchi, Hideyuki, Kurihara, Yuji, Doi, Hiroshi, Kunii, Misako, Tanaka, Kenichi, Nakamura, Haruko, Fukai, Ryoko, Tomita-Katsumoto, Atsuko, Tada, Mikiko, Higashiyama, Yuichi, Joki, Hideto, Koyano, Shigeru, Takei, Kohtaro, Tanaka, Fumiaki
Pubblicato in J Neuroinflammation (2018)

Duplication of the NPHP1 gene in patients with autism spectrum disorder and normal intellectual ability: a case series

di Yasuda, Yuka, Hashimoto, Ryota, Fukai, Ryoko, Okamoto, Nobuhiko, Hiraki, Yoko, Yamamori, Hidenaga, Fujimoto, Michiko, Ohi, Kazutaka, Taniike, Masako, Mohri, Ikuko, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Saitsu, Hirotomo, Matsumoto, Naomichi, Miyake, Noriko, Takeda, Masatoshi
Pubblicazione 2014

Phenotypic spectrum of GNAO1 variants: epileptic encephalopathy to involuntary movements with severe developmental delay

di Saitsu, Hirotomo, Fukai, Ryoko, Ben-Zeev, Bruria, Sakai, Yasunari, Mimaki, Masakazu, Okamoto, Nobuhiko, Suzuki, Yasuhiro, Monden, Yukifumi, Saito, Hiroshi, Tziperman, Barak, Torio, Michiko, Akamine, Satoshi, Takahashi, Nagahisa, Osaka, Hitoshi, Yamagata, Takanori, Nakamura, Kazuyuki, Tsurusaki, Yoshinori, Nakashima, Mitsuko, Miyake, Noriko, Shiina, Masaaki, Ogata, Kazuhiro, Matsumoto, Naomichi
Pubblicato in Eur J Hum Genet (2016)

Biallelic TBCD Mutations Cause Early-Onset Neurodegenerative Encephalopathy

di Miyake, Noriko, Fukai, Ryoko, Ohba, Chihiro, Chihara, Takahiro, Miura, Masayuki, Shimizu, Hiroshi, Kakita, Akiyoshi, Imagawa, Eri, Shiina, Masaaki, Ogata, Kazuhiro, Okuno-Yuguchi, Jiu, Fueki, Noboru, Ogiso, Yoshifumi, Suzumura, Hiroshi, Watabe, Yoshiyuki, Imataka, George, Leong, Huey Yin, Fattal-Valevski, Aviva, Kramer, Uri, Miyatake, Satoko, Kato, Mitsuhiro, Okamoto, Nobuhiko, Sato, Yoshinori, Mitsuhashi, Satomi, Nishino, Ichizo, Kaneko, Naofumi, Nishiyama, Akira, Tamura, Tomohiko, Mizuguchi, Takeshi, Nakashima, Mitsuko, Tanaka, Fumiaki, Saitsu, Hirotomo, Matsumoto, Naomichi
Pubblicato in Am J Hum Genet (2016)