Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Toshiki Tsunogai"'
Autor:
Toshiki Tsunogai, Toya Ohashi, Yohta Shimada, Takashi Higuchi, Ayaka Kimura, Ayako M. Watabe, Fusao Kato, Hiroyuki Ida, Hiroshi Kobayashi
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 25, Iss , Pp 448-460 (2022)
GM1-gangliosidosis is a progressive neurodegenerative glycosphingolipidosis resulting from a GLB1 gene mutation causing a deficiency of the lysosomal enzyme β-galactosidase, which leads to the abnormal accumulation of GM1 ganglioside in the central
Externí odkaz:
https://doaj.org/article/7324db0761c5449a83b52405a909083c
Autor:
Wataru Ohyama, Masaharu Akiyama, Masayoshi Yamaoka, Takaya Honda, Toshiki Tsunogai, Atsuko Kusuhara
Publikováno v:
Journal of Pediatric and Adolescent Gynecology. 33:421-424
Background The appendix and ovaries are rarely involved simultaneously in malignancies. The decision to perform an ovarian biopsy or a surgical resection in young patients can be challenging without sufficient clinical information. Case We describe a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d920238ab8e0f34e6bd956d142127a77
https://doi.org/10.1016/j.jpag.2020.04.003
https://doi.org/10.1016/j.jpag.2020.04.003
Autor:
Toshiki Tsunogai, Toya Ohashi, Yohta Shimada, Takashi Higuchi, Ayaka Kimura, Ayako M. Watabe, Fusao Kato, Hiroyuki Ida, Hiroshi Kobayashi
Publikováno v:
Molecular therapy. Methodsclinical development. 25
GM1-gangliosidosis is a progressive neurodegenerative glycosphingolipidosis resulting from a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87bbd6d059746befc655314ac4d0d0f0
https://pubmed.ncbi.nlm.nih.gov/36186953
https://pubmed.ncbi.nlm.nih.gov/36186953
Autor:
Toshiki Tsunogai1 tsunogait@gmail.com, Ichiro Miyata2, Saori Kotake1, Ryuki Matsuura1, Ken Takagi1, Hiroyuki Nanba1, Noriko Takahata1, Toshihiro Tajima3, Yasuyuki Wada1
Publikováno v:
Clinical Pediatric Endocrinology. Jul2016, Vol. 25 Issue 3, p111-114. 4p. 1 Diagram, 1 Chart, 2 Graphs.
Autor:
Yasuyuki Wada, Ryuki Matsuura, Toshihiro Tajima, Toshiki Tsunogai, Noriko Takahata, Saori Kotake, Hiroyuki Nanba, Ken Takagi, Ichiro Miyata
Publikováno v:
Clinical Pediatric Endocrinology. 25:111-114
Pseudohypoaldosteronism type 1 (PHA1) is a rare disease characterized by congenital resistance to the action of aldosterone on epithelial tissue; PHA1 results in excessive salt wasting despite very high plasma aldosterone and renin levels (1,2,3). Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2896aa35e1bb6fc133aabad09102b2d
https://doi.org/10.1297/cpe.25.111
https://doi.org/10.1297/cpe.25.111