Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Nagaaki Katoh"'
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:
Yuki Shimamoto, Naoki Takahashi, Nagaaki Katoh, Yuki Matsui, Yusuke Mochizuki, Masanori Ito, Masahide Yazaki, Fuyuki Kametani, Kenji Kasuno, Yoshiki Sekijima, Hironobu Naiki, Masayuki Iwano
Publikováno v:
BMC Nephrology, Vol 24, Iss 1, Pp 1-8 (2023)
Abstract Background Light and heavy chain deposition disease (LHCDD) is a rare condition characterised by the deposition of immunoglobulin components in the kidneys. Similarly, Amyloidosis is also caused by the deposition of light chain and/or heavy
Externí odkaz:
https://doaj.org/article/cce1f7a819824074bbd697a34b45ff8f
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
Autor:
Shinsuke Morisaki, Shinji Tsuchida, Eiichi Konishi, Nagaaki Katoh, Yusuke Takahashi, Kenji Takahashi
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 2, Pp 305-311 (2021)
Amyloidosis is a disorder caused by extracellular tissue deposition of insoluble fibrils. Amyloidosis can be divided into systemic or localized disease. Primary systemic amyloidosis is a multisystem disease caused by the deposition of amyloid in vari
Externí odkaz:
https://doaj.org/article/78ff3c5996654d5fa510f094fe1685cd
Autor:
Tomomi Kinoshita, Kazuhiro Fukushima, Ryu-ta Abe, Yuka Ogawa, Michitaka Nakagawa, Nagaaki Katoh, Takuhiro Yoshida, Hiroyuki Kato, Shu-ichi Ikeda
Publikováno v:
Case Reports in Neurology, Vol 6, Iss 2, Pp 202-206 (2014)
Histological evaluation of a peripheral nerve is often the final diagnostic work-up for a neuropathy of unknown origin, and a distal sensory nerve is usually biopsied. Here, we report the case of a female patient with painful unilateral neuropathy in
Externí odkaz:
https://doaj.org/article/6accca2da58d4315b14061d511b91489
Autor:
Tanya L. Poshusta, Nagaaki Katoh, Morie A. Gertz, Angela Dispenzieri, Marina Ramirez-Alvarado
Publikováno v:
International Journal of Molecular Sciences, Vol 14, Iss 11, Pp 22604-22617 (2013)
Light chain (AL) amyloidosis is a devastating disease characterized by amyloid deposits formed by immunoglobulin light chains. Current available treatments involve conventional chemotherapy and autologous stem cell transplant. We have recently conclu
Externí odkaz:
https://doaj.org/article/80a033ae60e042e6942dc89a1c79b58c
Autor:
Kenshi Suzuki, Ashutosh D. Wechalekar, Kihyun Kim, Chihiro Shimazaki, Jin Seok Kim, Takayuki Ikezoe, Chang-Ki Min, Fude Zhou, Zhen Cai, Xiaonong Chen, Shinsuke Iida, Nagaaki Katoh, Tomoaki Fujisaki, Ho-Jin Shin, NamPhuong Tran, Xiang Qin, Sandra Y. Vasey, Brenda Tromp, Brendan M. Weiss, Raymond L. Comenzo, Efstathios Kastritis, Jin Lu
Publikováno v:
Annals of Hematology. 102:863-876
Subcutaneous daratumumab plus bortezomib/cyclophosphamide/dexamethasone (VCd; D-VCd) improved outcomes versus VCd for patients with newly diagnosed immunoglobulin light-chain (AL) amyloidosis in the phase 3 ANDROMEDA study. We report a subgroup analy
Publikováno v:
Internal Medicine. 61:1603-1608
A 41-year-old woman was diagnosed with polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome based on polyneuropathy, hepatosplenomegaly, sclerotic bone lesions, IgA-λ M-protein, and an elevated level of serum va
Autor:
Kazuna Ikeda, Daisuke Yamamoto, Keiko Usui, Hiroki Takeuchi, Nobuyuki Oka, Nagaaki Katoh, Masahide Yazaki, Fuyuki Kametani, Ichizo Nishino, Shin Hisahara
Publikováno v:
Internal Medicine.
Autor:
Kazuna, Ikeda, Daisuke, Yamamoto, Keiko, Usui, Hiroki, Takeuchi, Nobuyuki, Oka, Nagaaki, Katoh, Masahide, Yazaki, Fuyuki, Kametani, Ichizo, Nishino, Shin, Hisahara
Publikováno v:
Internal medicine (Tokyo, Japan).
We herein report a 68-year-old Japanese man with sporadic variant transthyretin (ATTRv) amyloidosis harboring the novel variant A97D (p.A117D) in TTR. He had slow development of asymmetric neuropathy, unintentional weight loss, mild autonomic failure