Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yuri Nawashiro"'
Autor:
Akira Shimizu, Shingo Yamanishi, Hidehisa Saeki, Yuri Nawashiro, Motoshi Hattori, Nobuko Mayumi, Takeshi Yanagihara, Emi Yanai, Toru Igarashi, Yasuhiko Itoh, Yoko Matano, Yujiro Tanabe
Publikováno v:
CEN Case Rep
IgA vasculitis (IgAV) is the most frequent form of vasculitis in childhood which classically presents with purpura of the lower extremities, joint pain or swelling and abdominal pain. Though it is a self-limiting disease, and its prognosis is general
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd4b2e864ea4927cb5ed0e44225e3f5e
https://pubmed.ncbi.nlm.nih.gov/34191240
https://pubmed.ncbi.nlm.nih.gov/34191240
Autor:
Yasuyuki Sato, Hideki Ishida, Masataka Hisano, Hiroko Chikamoto, Hideaki Imamura, Shohei Fuchinoue, Tomoo Yabuuchi, Kazunari Tanabe, Seisuke Sakamoto, Naoto Kaneko, Takayuki Miyai, Motoshi Hattori, Yuri Nawashiro, Yuko Akioka, Masayoshi Okumi, Kiyonobu Ishizuka, Kenichiro Miura, Mureo Kasahara
Publikováno v:
Pediatric Transplantation. 24
Management of children with autosomal recessive polycystic kidney disease (ARPKD) who develop end-stage renal disease (ESRD) remains challenging because of concomitant liver disease. Patients with recurrent cholangitis are candidates for liver-kidney
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::764b7366ac0ecd73ec8e7431ff066cd7
https://doi.org/10.1111/petr.13690
https://doi.org/10.1111/petr.13690
Autor:
Motoshi Hattori, Kenichiro Miura, Keiichi Takizawa, Masataka Hisano, Shota Yamamoto, Kimiyasu Shiraki, Yuri Nawashiro, Yohei Sasada, Mamiko Suehiro, Toru Daikoku
Publikováno v:
Transplantation proceedings. 50(10)
Background Cytomegalovirus (CMV) could cause rejection in immunocompromised patients during early post-renal transplant stage. The American Transplant Society guidelines recommend prophylactic therapy with ganciclovir (GCV) for 3 to 6 months to preve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36cc1a5dce83e1bdf37ca2feabd05761
https://pubmed.ncbi.nlm.nih.gov/30577289
https://pubmed.ncbi.nlm.nih.gov/30577289
Autor:
Kazumoto Iijima, Shoichiro Kanda, Kei Nishiyama, Yuko Akioka, Norimasa Tada, Naoya Morisada, Kiyonobu Ishizuka, Naoto Kaneko, Hiroko Chikamoto, Yuri Nawashiro, Motoshi Hattori, Noriko Sugawara, Tomoo Yabuuchi, Takayuki Miyai
Publikováno v:
Pediatric transplantation. 20(3)
CAKUT are the most frequent causes of ESRD in children. Mutations in the gene encoding HNF1B, a transcription factor involved in organ development and maintenance, cause a multisystem disorder that includes CAKUT, diabetes, and liver dysfunction. Her
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f3dd88fbf4d8083eb58d7d2c4753a7e
https://pubmed.ncbi.nlm.nih.gov/26899772
https://pubmed.ncbi.nlm.nih.gov/26899772