Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Katsuya Tashiro"'
Publikováno v:
Frontiers in Medicine, Vol 10 (2024)
Carbamoyl-phosphate synthetase 1 (CPS1) deficiency is an autosomal recessive congenital urea cycle disorder (UCD) characterized by hyperammonemia. The recipients of liver transplantation (LT) for UCD are often children, and the potential donors are o
Externí odkaz:
https://doaj.org/article/abfd4e0525994788a5055140043d8a57
Autor:
Kozo Nagai, Yukari Suyama, Daisuke Koga, Masanori Nishi, Chiaki Iida, Katsuya Tashiro, Atsushi Danjo, Keita Kai, Muneaki Matsuo
Publikováno v:
Case Reports in Oncology, Vol 9, Iss 2, Pp 440-446 (2016)
We described an 11-year-old boy suffering from pediatric anaplastic lymphoma kinase-positive anaplastic large cell lymphoma with heart metastasis at diagnosis and arterial tumor embolisms during chemotherapy. Both the heart metastasis and pericardial
Externí odkaz:
https://doaj.org/article/5226fb21aedd4016b3540eaacbdf40ea
Autor:
Yuya Ito, Toshihiko Kakiuchi, Hidenori Hidaka, Aiko Ikeuchi, Koichi Miyahara, Katsuya Tashiro
Publikováno v:
Indian Journal of Pediatrics. 90:193-194
Autor:
Muneaki Matsuo, Keiko Uda, Daisuke Tajima, Katsuya Tashiro, Takuji Nakamura, Rie Furukawa, Yuko Tomonoh, Nobuhiko Okamoto, Fumio Ichinose
Publikováno v:
Brain and Development. 43:482-485
Paroxysmal abnormal eye movement in early infancy is one of the initial symptoms of glucose transporter 1 deficiency syndrome (GLUT1DS). We describe four early infants with transient hypoglycorrhachia presenting with abnormal eye movements. Their sym
Autor:
Keigo Matsuyuki, Mizuki Ide, Keishirou Houjou, Saho Shima, Seiji Tanaka, Yoriko Watanabe, Hiroyuki Tomino, Tomoko Egashira, Toshimitsu Takayanagi, Katsuya Tashiro, Ken Okamura, Tamio Suzuki, Takayuki Miyamoto, Hirofumi Shibata, Takahiro Yasumi, Ryuta Nishikomori
Publikováno v:
Pediatric Allergy and Immunology. 33
Autor:
Keigo Matsuyuki, Mizuki Ide, Keishirou Houjou, Saho Shima, Seiji Tanaka, Yoriko Watanabe, Tomoko Egashira, Hiroyuki Tomino, Toshimitsu Takayanagi, Katsuya Tashiro, Ken Okamura, Tamio Suzuki, Ryuta Nishikomori
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ea575cc6b10fc0c48b9cffff1696a11
https://doi.org/10.22541/au.163253088.81986585/v1
https://doi.org/10.22541/au.163253088.81986585/v1
Publikováno v:
Pediatric Cardiology and Cardiac Surgery. 33:326-331
Autor:
Nobuhiko Okamoto, Tadashi Matsumoto, Yuri Dowa, Yasutsugu Chinen, Masafumi Fukuda, Kenji Shimizu, Katsuya Tashiro, Seiji Mizuno, Kyoko Minagawa, Yoko Hiraki, Yoshihiro Toda, Osamu Shimokawa, Toshiyuki Yamamoto, Hirofumi Ohashi, Satoshi Watanabe, Seijiro Aso, Koichi Shichijo, Natsuko Shiomi, Kazunori Minatozaki, Tatsuro Kondoh, Hiroyuki Moriuchi, Keiko Shimojima, Rika Kosaki, Koh-ichiro Yoshiura
Publikováno v:
American Journal of Medical Genetics Part A. 170:908-917
Partial 1q trisomy syndrome is a rare disorder. Because unbalanced chromosomal translocations often occur with 1q trisomy, it is difficult to determine whether patient symptoms are related to 1q trisomy or other chromosomal abnormalities. The present
Publikováno v:
Pediatric Cardiology and Cardiac Surgery. 32:43-47
Autor:
Yuhei Hamasaki, Hirohito Doi, Masafumi Zaitsu, Katsuya Tashiro, Yukiko Inada, Muneaki Matsuo, Chiduru Hayashi
Publikováno v:
Pediatrics International. 55:792-794
We describe a 15-day-old newborn girl who was fed with formula milk that was accidentally diluted with sake (Japanese wine prepared from fermented rice). The clinical features were flushed skin, tachycardia and low blood pressure indicating circulato