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Autor:
Satoshi Okada, Akinori Miyazono, Yasuhiro Inaba, Rumiko Eura, Toshihiko Itesako, Yoshifumi Kawano, Yasuhiro Okamoto
Publikováno v:
CEN Case Rep
Persistent cloaca involves fusion of the bladder, vagina, and rectum into a single duct called the common duct. Although its pathogenesis remains unclear, it has been associated with hyperchloremic metabolic acidosis. Herein, we present the case of a
Autor:
Yuichi Kodama, Shinsuke Maruyama, Shunji Seki, Manaka Matsunaga, Takayuki Tanabe, Junichiro Nishi, Akinori Miyazono, Michiyoshi Yoshimura, Yoshifumi Kawano
Publikováno v:
Brain and Development. 40:439-442
We report the case of a 12-year-old girl who developed Guillain-Barré syndrome (GBS) and optic neuritis (ON) following Mycoplasma pneumoniae infection. Her symptoms, including bilateral vision impairment and tingling in her hands and right foot, wer
Publikováno v:
Clinical Rheumatology. 36:433-437
Lupus nephritis is identified in up to 75% of patients with juvenile systemic lupus erythematosus and may present with abnormal urinary findings (overt lupus nephritis) or be apparent only upon renal biopsy (silent lupus nephritis). We investigated w
Autor:
Takanari Abematsu, Yasuhiro Okamoto, Akinori Miyazono, Shunsuke Nakagawa, Takuro Nishikawa, Yuichi Shinkoda, Yuichi Kodama, Naohiro Ikeda, Yoshifumi Kawano, Shunji Seki, Hiroyuki Wakiguchi, Koichiro Kurauchi, Takayuki Tanabe
Publikováno v:
Pediatric Transplantation. 20:329-332
Stenotrophomonas maltophilia causes pneumonia and CVC-CRBSI in HSCT. However, there are few reports of pyomyositis due to S. maltophilia. We report a patient with CRBSI and pyomyositis due to S. maltophilia after allogeneic HSCT who was successfully
Autor:
Rika Fujimaru, Ming Juan Ye, Koichi Nakanishi, Masafumi Matsuo, Koichi Kamei, Junya Fujimura, Aya Imafuku, Shogo Minamikawa, Kazumoto Iijima, Tomoko Horinouchi, Mitsuhiro Kawano, Emi Sawanobori, Kandai Nozu, Tomohiko Yamamura, Toru Igarashi, Chizuko Kitabayashi, Yoshimi Nozu, Masafumi Oka, Naoya Morisada, Hiroshi Kaito, Mineaki Kitamura, Yuko Shima, Akira Ashida, Kenjirou Okamoto, Keiichi Tamagaki, Keita Nakanishi, Akinori Miyazono, Takashi Omori, Shuichiro Fujinaga, Wataru Shimabukuro
Background X-linked Alport syndrome (XLAS) is a progressive hereditary nephropathy caused by mutations in the COL4A5 gene. Genotype-phenotype correlation in male XLAS is relatively well established; relative to truncating mutations, nontruncating mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::921b9afe4b4edea1ddb1083863a3e609
https://europepmc.org/articles/PMC6065097/
https://europepmc.org/articles/PMC6065097/
Autor:
Kentaro, Ueno, Shunji, Seki, Naohiro, Shiokawa, Tomoyuki, Matsuba, Akinori, Miyazono, Daisuke, Hazeki, Yutaka, Imoto, Yoshifumi, Kawano
Publikováno v:
Nephrology (Carlton, Vic.). 24(3)
We aimed to validate the incidence of, risk factors for, and postoperative outcomes of acute kidney injury (AKI) according to the modified Kidney Disease Improving Global Outcomes (m-KDIGO) criteria and compare this criteria with both the paediatric
Autor:
Takuya Fujimaru, Shuichi Ito, Koichi Kamei, Akinori Miyazono, Masao Ogura, Tomoaki Ishikawa, Mai Sato
Publikováno v:
Nihon Shoni Jinzobyo Gakkai Zasshi. 24:179-186
Autor:
Takako Yoshioka, Yuko Hamasaki, Yoshifumi Kawano, Hironobu Nagasako, Yasuhiro Okamoto, Seiichiro Shishido, Akinori Miyazono
Publikováno v:
American journal of kidney diseases : the official journal of the National Kidney Foundation. 68(3)
Posttransplantation lymphoproliferative disorder (PTLD) is associated with significant mortality in kidney transplant recipients. PTLD cases associated with poor prognostic factors that are refractory to reduction of immunosuppression generally requi
Autor:
Manaka Matsunaga, Hiroyuki Wakiguchi, Yoshifumi Kawano, Yuichi Kodama, Naohiro Ikeda, Shunji Seki, Yasuhiro Okamoto, Akinori Miyazono
Publikováno v:
Japanese Journal of Infectious Diseases. 69:424-425
Cat scratch disease (CSD) is an infectious disease caused by Bartonella henselae. Atypical clinical presentations of CSD include prolonged fever and multiple hepatosplenic lesions. Furthermore, multiple renal lesions are extremely rare in CSD. An 11-