Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Saki Oshiro"'
Publikováno v:
eNeurologicalSci, Vol 25, Iss , Pp 100387- (2021)
Externí odkaz:
https://doaj.org/article/c00034d2bac3409cb0bb3df1d947c8f1
Autor:
Ai Kawamoto-Hirano, Ryoukichi Ikeda, Toshiaki Takahashi, Sayaka Taniguchi, Masaru Yoshioka, Hiroyasu Tanaka, Hideki Oizumi, Tomoko Totsune, Saki Oshiro, Toru Baba, Atsushi Takeda, Yuta Kobayashi, Jun Ohta, Yukio Katori
Publikováno v:
Auris Nasus Larynx. 50:247-253
Aspiration pneumonia is one of the leading causes of death in patients with muscular dystrophy; therefore, it is important to predict its occurrence in the clincal setting. We aimed to examine the usefulness of repeated saliva swallowing test (RSST),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7051e19bac6e750ef00388d05b6d3282
https://doi.org/10.1016/j.anl.2022.07.006
https://doi.org/10.1016/j.anl.2022.07.006
Autor:
Tomonori Kambayashi, Ai Hirano-Kawamoto, Toshiaki Takahashi, Sayaka Taniguchi, Masaru Yoshioka, Hiroyasu Tanaka, Hideki Oizumi, Tomoko Totsune, Saki Oshiro, Toru Baba, Atsushi Takeda, Takuma Hisaoka, Jun Ohta, Ryoukichi Ikeda, Jun Suzuki, Kengo Kato, Yukio Katori
Publikováno v:
Auris, nasus, larynx. 49(6)
The objectives of the study were to clarify the characteristics of dysphagia and the incidence of pneumonia in Myotonic dystrophy type 1 (DM1) patients, and to investigate the relationship between the development of pneumonia and the DM1 patient's ba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abab1dd3199a63314e1cd159cb7c9030
https://pubmed.ncbi.nlm.nih.gov/35428520
https://pubmed.ncbi.nlm.nih.gov/35428520
Autor:
Natsumi Fujisaki, Masanori Nakagawa, Miwako Kido, Hiroshi Takashima, Ryo Nakachi, Saki Oshiro, Masahito Suehara, Yoshihisa Fujiwara, Shugo Suwazono, Takashi Tokashiki
Publikováno v:
Intractable & Rare Diseases Research. 7:7-12
Hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) is a motor and sensory neuronopathy with autosomal dominant inheritance, adult onset, slowly progressive course, and is associated with TRK-fused gene (TFG) mutation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cea5e420d3237b4b3dca08c51014af53
https://doi.org/10.5582/irdr.2017.01084
https://doi.org/10.5582/irdr.2017.01084