Management of Dysphagia in Patients with Parkinson's Disease and Related Disorders

por Umemoto, George, Furuya, Hirokazu
Publicado 2019

Freezing of gait is an early clinical feature of progressive supranuclear palsy

por Osaki, Yasushi, Morita, Yukari, Miyamoto, Yuka, Furuta, Kounosuke, Furuya, Hirokazu
Publicado 2017

Characteristics of tongue and pharyngeal pressure in patients with neuromuscular diseases

por Umemoto, George, Furuya, Hirokazu, Tsuboi, Yoshio, Fujioka, Shinsuke, Arahata, Hajime, Sugahara, Miwa, Sakai, Mitsuaki
Publicado 2017

Identification of a pre‐possible multiple system atrophy phase

por Osaki, Yasushi, Morita, Yukari, Miyamoto, Yuka, Ohtsuru, Sho, Shogase, Tomohiro, Furushima, Tomomi, Furuya, Hirokazu
Publicado 2020

Longitudinal Changes of Tongue Thickness and Tongue Pressure in Neuromuscular Disorders

por Umemoto, George, Fujioka, Shinsuke, Arahata, Hajime, Sakae, Nobutaka, Sasagasako, Naokazu, Toda, Mine, Furuya, Hirokazu, Tsuboi, Yoshio
Publicado 2021

Dysphagia in Perry Syndrome: Pharyngeal Pressure in Two Cases

por Umemoto, George, Tsuboi, Yoshio, Furuya, Hirokazu, Mishima, Takayasu, Fujioka, Shinsuke, Fujii, Naoki, Arahata, Hajime, Sugahara, Miwa, Sakai, Mitsuaki
Publicado 2017

Novel Drug Candidates Improve Ganglioside Accumulation and Neural Dysfunction in GM1 Gangliosidosis Models with Autophagy Activation

por Kajihara, Ryutaro, Numakawa, Tadahiro, Odaka, Haruki, Yaginuma, Yuji, Fusaki, Noemi, Okumiya, Toshika, Furuya, Hirokazu, Inui, Seiji, Era, Takumi
Publicado 2020

Supplemental Treatment for Huntington’s Disease with miR-132 that Is Deficient in Huntington’s Disease Brain

por Fukuoka, Masashi, Takahashi, Masaki, Fujita, Hiromi, Chiyo, Tomoko, Popiel, H. Akiko, Watanabe, Shoko, Furuya, Hirokazu, Murata, Miho, Wada, Keiji, Okada, Takashi, Nagai, Yoshitaka, Hohjoh, Hirohiko
Publicado 2018

Atypical Familial Amyotrophic Lateral Sclerosis with Slowly Progressing Lower Extremities-predominant Late-onset Muscular Weakness and Atrophy

por Togawa, Jumpei, Ohi, Takekazu, Yuan, Jun-Hui, Takashima, Hiroshi, Furuya, Hirokazu, Takechi, Shinji, Fujitake, Junko, Hayashi, Saki, Ishiura, Hiroyuki, Naruse, Hiroya, Mitsui, Jun, Tsuji, Shoji
Publicado 2019

Association of right precuneus compression with apathy in idiopathic normal pressure hydrocephalus: a pilot study

por Chadani, Yoshihiro, Kashibayashi, Tetsuo, Yamamoto, Takahiro, Tsuda, Atsushi, Fujito, Ryoko, Akamatsu, Masanori, Kamimura, Naoto, Takahashi, Ryuichi, Yamagami, Takuji, Furuya, Hirokazu, Ueba, Tetsuya, Saito, Motoaki, Inoue, Keiji, Kazui, Hiroaki
Publicado 2022

Medication tendencies for inducing severe ocular surface symptoms in Japanese Stevens-Johnson Syndrome / toxic epidermal necrolysis patients

por Saito, Yoshiro, Ueta, Mayumi, Nakamura, Ryosuke, Sugiyama, Emiko, Maekawa, Keiko, Takahashi, Yukitoshi, Furuya, Hirokazu, Yagami, Akiko, Matsukura, Setsuko, Ikezawa, Zenro, Matsunaga, Kayoko, Sotozono, Chie, Aihara, Michiko, Kinoshita, Shigeru, Kaniwa, Nahoko
Publicado 2014

Independent strong association of HLA-A*02:06 and HLA-B*44:03 with cold medicine-related Stevens-Johnson syndrome with severe mucosal involvement

por Ueta, Mayumi, Kaniwa, Nahoko, Sotozono, Chie, Tokunaga, Katsushi, Saito, Yoshiro, Sawai, Hiromi, Miyadera, Hiroko, Sugiyama, Emiko, Maekawa, Keiko, Nakamura, Ryosuke, Nagato, Masaki, Aihara, Michiko, Matsunaga, Kayoko, Takahashi, Yukitoshi, Furuya, Hirokazu, Muramatsu, Masaaki, Ikezawa, Zenrou, Kinoshita, Shigeru
Publicado 2014

An association analysis of HLA-DQB1 with narcolepsy without cataplexy and idiopathic hypersomnia with/without long sleep time in a Japanese population

por Miyagawa, Taku, Toyoda, Hiromi, Kanbayashi, Takashi, Imanishi, Aya, Sagawa, Yohei, Kotorii, Nozomu, Kotorii, Tatayu, Hashizume, Yuji, Ogi, Kimihiro, Hiejima, Hiroshi, Kamei, Yuichi, Hida, Akiko, Miyamoto, Masayuki, Ikegami, Azusa, Wada, Yamato, Takami, Masanori, Fujimura, Yota, Tamura, Yoshiyuki, Omata, Naoto, Masuya, Yasuhiro, Kondo, Hideaki, Moriya, Shunpei, Furuya, Hirokazu, Kato, Mitsuhiro, Kojima, Hiroto, Kashiwase, Koichi, Saji, Hiroh, Khor, Seik-Soon, Yamasaki, Maria, Ishigooka, Jun, Wada, Yuji, Chiba, Shigeru, Yamada, Naoto, Okawa, Masako, Kuroda, Kenji, Kume, Kazuhiko, Hirata, Koichi, Uchimura, Naohisa, Shimizu, Tetsuo, Inoue, Yuichi, Honda, Yutaka, Mishima, Kazuo, Honda, Makoto, Tokunaga, Katsushi
Publicado 2015

A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia

por Miyagawa, Taku, Tanaka, Susumu, Shimada, Mihoko, Sakai, Noriaki, Tanida, Kotomi, Kotorii, Nozomu, Kotorii, Tatayu, Ariyoshi, Yu, Hashizume, Yuji, Ogi, Kimihiro, Hiejima, Hiroshi, Kanbayashi, Takashi, Imanishi, Aya, Ikegami, Azusa, Kamei, Yuichi, Hida, Akiko, Wada, Yamato, Miyamoto, Masayuki, Takami, Masanori, Kondo, Hideaki, Tamura, Yoshiyuki, Taniyama, Yukari, Omata, Naoto, Mizuno, Tomoyuki, Moriya, Shunpei, Furuya, Hirokazu, Kato, Mitsuhiro, Kato, Kayoko, Ishigooka, Jun, Tsuruta, Kazuhito, Chiba, Shigeru, Yamada, Naoto, Okawa, Masako, Hirata, Koichi, Kuroda, Kenji, Kume, Kazuhiko, Uchimura, Naohisa, Kitada, Masaaki, Kodama, Tohru, Inoue, Yuichi, Nishino, Seiji, Mishima, Kazuo, Tokunaga, Katsushi, Honda, Makoto
Publicado 2022