Transient thyrotoxicosis‐aggravated attacks of paralysis in a patient with hereditary hypokalemic periodic paralysis type 2 von Nagamatsu, Shu‐ichi, Osaki, Yasushi, Morita, Yukari, Miyamoto, Yuka, Mori, Itsuki, Kubota, Tomoya, Takahashi, Masanori P., Furushima, Tomomi, Furuya, Hirokazu

Volltext

A novel nonsense mutation in the TITF-1 gene in a Japanese family with benign hereditary chorea von Nakamura, Katsuya, Sekijima, Yoshiki, Nagamatsu, Kiyoshiro, Yoshida, Kunihiro, Ikeda, Shu-ichi

Volltext

Cerebral hemorrhage in Fabry's disease von Nakamura, Katsuya, Sekijima, Yoshiki, Nakamura, Kimitoshi, Hattori, Kiyoko, Nagamatsu, Kiyoshiro, Shimizu, Yusaku, Yasude, Takuji, Ushiyama, Masao, Endo, Fumio, Fukushima, Yoshimitsu, Ikeda, Shu-ichi

Volltext

Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan von Misu, Ken-ichiro, Hattori, Naoki, Nagamatsu, Masaaki, Ikeda, Shu-ichi, Ando, Yukio, Nakazato, Masamitsu, Takei, Yo-ichi, Hanyu, Norinao, Usui, Yasuomi, Tanaka, Fumiaki, Harada, Toshihide, Inukai, Akira, Hashizume, Yoshio, Sobue, Gen

Volltext