Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Tsuneaki, Yoshinaga"'
Lysinuric protein intolerance exhibiting renal tubular acidosis/Fanconi syndrome in a Japanese woman
Autor:
Hiroaki Hanafusa, Katsuya Nakamura, Yuji Kamijo, Masashi Kitahara, Takashi Ehara, Tsuneaki Yoshinaga, Kaoru Aoki, Nagaaki Katoh, Tomomi Yamaguchi, Tomoki Kosho, Yoshiki Sekijima
Publikováno v:
JIMD Reports, Vol 64, Iss 6, Pp 410-416 (2023)
Abstract Lysinuric protein intolerance (LPI), caused by pathogenic variants of SLC7A7, is characterized by protein aversion, failure to thrive, hyperammonemia, and hepatomegaly. Recent studies have reported that LPI can cause multiple organ dysfuncti
Externí odkaz:
https://doaj.org/article/4dcd043c46e94891b20f8e4231327cd4
Autor:
Shojiro Ichimata, Yukiko Hata, Tsuneaki Yoshinaga, Nagaaki Katoh, Fuyuki Kametani, Masahide Yazaki, Yoshiki Sekijima, Naoki Nishida
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 7, p 4040 (2024)
This study aimed to elucidate the similarities and differences between amyloid-forming corpora amylacea (CA) in the prostate and lung, examine the nature of CAs in cystic tumors of the atrioventricular node (CTAVN), and clarify the distinctions betwe
Externí odkaz:
https://doaj.org/article/e1b671f8ea4b44cf9126280907a797f8
Akademický článek
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Autor:
Junya Kitahara, Tsuneaki Yoshinaga, Shinji Kakihara, Takao Hirano, Akira Imai, Teruyoshi Miyahara, Masahide Yazaki, Yoshiki Sekijima, Toshinori Murata
Publikováno v:
PLoS ONE, Vol 18, Iss 9, p e0291716 (2023)
PurposeTo investigate the presence of amyloidosis-related ocular findings in patients who received domino liver transplantation from ATTRv amyloidosis donors.MethodsWe reviewed the ocular findings in patients who had previously undergone domino liver
Externí odkaz:
https://doaj.org/article/f9b0dfe532ef4e908e3dce16770d4ec6
Autor:
Goichi Beck, Yuki Yonenobu, Makiko Kawai, Kensuke Ikenaka, Fusako Sera, Tatsuhiko Ozono, Yuki Shimada, Rika Yamashita, Yasushi Sakata, Eiichi Morii, Tsuneaki Yoshinaga, Yukio Ando, Shigeo Murayama, Hideki Mochizuki
Publikováno v:
Journal of Neurology.
Autor:
Katsuya Nakamura, Tsuneaki Yoshinaga, Minori Kodaira, Emiko Kise, Tomoki Kosho, Yoshiki Sekijima
Publikováno v:
Internal Medicine; 2023, Vol. 62 Issue 20, p3047-3051, 5p
Autor:
Kaname Uno, Tomoyuki Koike, Takeshi Kanno, Kenichiro Nakagawa, Naoki Asano, Masahiro Saito, Akira Imatani, Fumiyoshi Fujishima, Kiyotaka Asanuma, Tsuneaki Yoshinaga, Taku Fujiya, Yohei Ogata, Atsushi Masamune, Nagaaki Katoh, Waku Hatta, Xiaoyi Jin
Publikováno v:
Internal Medicine
A 72-year-old man without any symptoms was referred to our hospital. Esophagogastroduodenoscopy revealed an elevated esophageal lesion that was covered with normal mucosa. The examination of biopsy specimens from the lesion revealed amyloid light-cha
Autor:
Yasufumi, Kondo, Tsuneaki, Yoshinaga, Katsuya, Nakamura, Tomomi, Yamaguchi, Masumi, Ishikawa, Tomoki, Kosho, Yoshiki, Sekijima
Publikováno v:
Neurology. Genetics. 9(1)
To investigate the clinical effect of a heterozygous missense variant ofWe performed clinical, laboratory, radiologic, and genetic evaluations of members of a previously reported family with cerebral autosomal recessive arteriopathy with subcortical
Autor:
Fumiyoshi Fujishima, Tomoyuki Handa, Yusuke Shimoyama, Atsushi Masamune, Tsuneaki Yoshinaga, Yoshitake Kanazawa, Kasumi Hishinuma, Takeo Naito, Masahide Yazaki, Masatake Kuroha, Kaoru Suzuki, Yutaro Masu, Rintaro Moroi, Yoichi Kakuta, Hisashi Shiga
Publikováno v:
Clinical Journal of Gastroenterology. 14:815-819
Amyloidosis is classifiable as systemic, with amyloid deposition in organs throughout the body, or localized, involving only one organ. Amyloidosis localized in the intestinal tract is rare. This report describes three cases of localized AL amyloidos
Autor:
Masahide Yazaki, Fuyuki Kametani, Yoshiki Sekijima, Nagaaki Katoh, Tsuneaki Yoshinaga, Keiichi Higuchi, Mayuko Nakagawa
Publikováno v:
Pathology International. 71:245-254
It is difficult to diagnose immunoglobulin heavy chain amyloidosis (AH amyloidosis) without proteomic analysis due to no useful diagnostic antibodies. The aim of this study was to develop diagnostic antibodies available to immunohistochemistry and im