Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Takahiko Seo"'
Publikováno v:
Journal of Hepato-Biliary-Pancreatic Surgery. 16:339-345
We hypothesized neuronal disorders of the biliary tract as the cause of congenital biliary dilation (CBD).Gallbladders were removed from a total of 15 patients who were categorized into two study groups: a CBD group (eight patients) and in a control
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53f9d8408a82d51a73d80f4c45711c33
https://doi.org/10.1007/s00534-009-0066-x
https://doi.org/10.1007/s00534-009-0066-x
Autor:
Atsuo Itakua, Seiji Hayashi, Yoshiaki Sato, Seiji Kojima, Atsushi Nakayama, Akiko Saito, Seiji Sumigama, Masayuki Hasegawa, Kenitiro Kaneko, Megumi Miyauchi, Hisami Ando, Koji Takemoto, Takahiko Seo, Masahiro Hayakawa, Fumitaka Kikkawa, Hiromi Hayakawa, Mayumi Okada
Publikováno v:
Pediatric Research. 62:93-97
We evaluated whether a correlation existed between fetal pulmonary magnetic resonance imaging (MRI) findings and postnatal mortality, as well as the requirements for extracorporeal membrane oxygenation (ECMO) in infants with prenatally diagnosed, iso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a905cca6c4517a41c93207e1a729109
https://doi.org/10.1203/pdr.0b013e3180676cdb
https://doi.org/10.1203/pdr.0b013e3180676cdb
Publikováno v:
Digestive Diseases and Sciences. 52:1979-1986
Symptoms of choledochal cysts are caused by protein plugs. We performed proteomic analysis of protein plugs to elucidate formation mechanism. Protein plugs were obtained from three pediatric patients with choledochal cyst. Proteins were separated usi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bee1d2a9134efb1f4735bb6b0e0decdc
https://doi.org/10.1007/s10620-006-9398-4
https://doi.org/10.1007/s10620-006-9398-4
Autor:
Takahisa Tainaka, Wataru Sumida, Takahiko Seo, Yukio Ogura, Kenitiro Kaneko, Hisami Ando, Tetsuya Kiuchi, Yasuyuki Ono
Publikováno v:
Journal of Pediatric Surgery. 41:e9-e12
Congenital absence of the portal vein (CAPV) requires liver transplantation when encephalopathy develops. However, transplantation has technical difficulties because no collateral circulation exists except for the portosystemic shunt. Ligating the sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10145d08310198dc4f88399219e6dbd4
https://doi.org/10.1016/j.jpedsurg.2006.07.014
https://doi.org/10.1016/j.jpedsurg.2006.07.014
Autor:
Kenitiro Kaneko, Takahisa Tainaka, Yukio Ogura, Hidemi Wada, Takahiko Seo, Chiyoe Shirota, Hisami Ando, Yasuyuki Ono
Publikováno v:
Journal of Pediatric Surgery. 41:808-811
Background Hepatolithiasis after hepatic portoenterostomy for biliary atresia has been paid little attention, with only 22 reported cases. Patients and Methods Fifteen patients underwent living-related liver transplantation for biliary atresia after
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a77cd8f5b3d67359cbe09ecde0228184
https://doi.org/10.1016/j.jpedsurg.2005.12.036
https://doi.org/10.1016/j.jpedsurg.2005.12.036
Publikováno v:
Journal of Pediatric Surgery. 41:812-816
Background/Purpose The cause of extrahepatic portal hypertension in children has not been clarified. Our aim was to determine the morphological features of the extrahepatic portal vein in children with extrahepatic portal hypertension by 3-dimensiona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74e1c0377d93b68bb20497ead64f3a71
https://doi.org/10.1016/j.jpedsurg.2005.12.027
https://doi.org/10.1016/j.jpedsurg.2005.12.027
Publikováno v:
Pediatric Surgery International. 21:8-11
Intrahepatic calculi complicate choledochal cysts in 7–8% of patients. Although congenital stenoses and dilatation of the intrahepatic bile ducts are considered responsible for calculi formation, intrahepatic calculi are usually formed after cyst e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b26a78e707a52ec4c4078ef04eaa979
https://doi.org/10.1007/s00383-004-1253-0
https://doi.org/10.1007/s00383-004-1253-0
Publikováno v:
Artificial Organs. 27:192-198
For safer and simpler neonatal ECMO management, the authors have been developing an innovative, automatically-controlled ECMO machine using self-regulating blood pumps. The newest model is an air-driven, tube-type blood pump. A pair of blood pumps ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60e2c9a58c99e24d4b925465dea73fc4
https://doi.org/10.1046/j.1525-1594.2003.t01-3-06993.x
https://doi.org/10.1046/j.1525-1594.2003.t01-3-06993.x
Autor:
Hisami Ando, Yoshio Watanabe, Yasuyuki Ono, Shinsuke Katsuno, Yuji Marui, Takahiko Seo, Shigeko Torihashi
Publikováno v:
Pediatrics International. 44:145-148
Background: Esophageal achalasia (EA) is a rare disease in children, the etiology and pathogenesis of which remain controversial. Previous studies have suggested that a specific class of interstitial cells of Cajal (ICC) act as mediators in nitrergic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddd297a04817364b20e19aae734abf19
https://doi.org/10.1046/j.1442-200x.2002.01518.x
https://doi.org/10.1046/j.1442-200x.2002.01518.x
Autor:
Akimasa Nakao, Yuji Marui, Takahiko Seo, Tetsuya Kaneko, Hisami Ando, Hiroyuki Sugimoto, Soichiro Inoue, Tsuyoshi Hatsuno
Publikováno v:
Journal of Hepato-Biliary-Pancreatic Surgery. 8:573-576
Portal hepatofugal flow is rare after liver transplantation. We experienced a case in which hepatofugal portal flow was observed in acute rejection. A 6-year-old boy with glycogen storage disease type Ia underwent living-donor liver transplantation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7251802de70f6c03c543c11ab34d0887
https://doi.org/10.1007/s005340100028
https://doi.org/10.1007/s005340100028