An altered GABA-A receptor function in spinocerebellar ataxia type 6 and familial hemiplegic migraine type 1 associated with the CACNA1A gene mutation

por Kono, Satoshi, Terada, Tatsuhiro, Ouchi, Yasuomi, Miyajima, Hiroaki
Publicado 2014

Ascending aortic cannulation for Stanford type A acute aortic dissection

por Iwakura, Atsushi, Hori, Yuki, Kono, Satoshi, Yamanaka, Kazuo
Publicado 2015

A Video Report of Brain–Lung–Thyroid Syndrome in a Japanese Female With a Novel Frameshift Mutation of the NKX2-1 Gene

por Tozawa, Takenori, Yokochi, Kenji, Kono, Satoshi, Konishi, Takashi, Yamamoto, Toshiyuki, Nishimura, Akira, Chiyonobu, Tomohiro, Morimoto, Masafumi, Hosoi, Hajime
Publicado 2016

Aceruloplasminemia with Abnormal Compound Heterozygous Mutations Developed Neurological Dysfunction during Phlebotomy Therapy

por Watanabe, Maki, Ohyama, Ken, Suzuki, Masashi, Nosaki, Yasunobu, Hara, Takashi, Iwai, Katsushige, Kono, Satoshi, Miyajima, Hiroaki, Mokuno, Kenji
Publicado 2018

The Resection of Thyroid Cancer Was Associated with the Resolution of Hyporesponsiveness to an Erythropoiesis-stimulating Agent in a Hemodialysis Patient with Aceruloplasminemia

por Nagata, Soichiro, Ikegaya, Naoki, Ogino, Shuhei, Uchida, Shinichi, Itaya, Mikiko, Momita, Aoi, Shinozaki, Shingo, Ohura, Masaharu, Kuriki, Ken, Kono, Satoshi, Miyajima, Hiroaki, Hishida, Akira
Publicado 2017