Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Ryo Shirotsuki"'
Autor:
Naruhiko Murase, Takahisa Tainaka, Hiroo Uchida, Akinari Hinoki, Chiyoe Shirota, Kazuki Yokota, Kazuo Oshima, Ryo Shirotsuki, Kosuke Chiba, Yujiro Tanaka
Publikováno v:
Journal of Investigative Surgery, Vol 32, Iss 1, Pp 55-60 (2019)
Purpose: Experimental models of laparoscopic surgery generally use large animals owing to a sufficient abdominal working space. We developed a novel laparoscopic surgery model in rats. We performed intestinal anastomosis to demonstrate the feasibilit
Externí odkaz:
https://doaj.org/article/7246906d73a346ca9f2b9d08f778247b
Autor:
Chiyoe Shirota, Takahisa Tainaka, Toshiki Nakane, Yujiro Tanaka, Akinari Hinoki, Wataru Sumida, Naruhiko Murase, Kazuo Oshima, Kosuke Chiba, Ryo Shirotsuki, Hiroo Uchida
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-5 (2018)
Abstract Background Emergency rescue lung resection is rarely performed to treat congenital lung cysts (CLCs) in neonates. Many reports have described fetal CLC treatment; however, prenatal predictors for postnatal respiratory failure have not been c
Externí odkaz:
https://doaj.org/article/8a739a93d7a0456882f67c716cb2ba3c
Autor:
Kazuo Oshima, Hiroo Uchida, Takahisa Tainaka, Akihide Tanano, Chiyoe Shirota, Kazuki Yokota, Naruhiko Murase, Ryo Shirotsuki, Kosuke Chiba, Akinari Hinoki
Publikováno v:
Journal of Minimal Access Surgery, Vol 13, Iss 1, Pp 73-75 (2017)
A right aortic arch (RAA) is found in 5% of neonates with tracheoesophageal fistulae (TEF) and may be associated with vascular rings. Oesophageal repairs for TEF with an RAA via the right chest often pose surgical difficulties. We report for the firs
Externí odkaz:
https://doaj.org/article/7c2524d272ef4dbdbcd3c1615ee62119
Autor:
Naruhiko Murase, Hiroo Uchida, Akihide Tanano, Chiyoe Shirota, Akinari Hinoki, Takahisa Tainaka, Kazuki Yokota, Kazuo Oshima, Ryo Shirotsuki
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 3, Iss 12, Pp 534-536 (2015)
Patients with hepatic arteriovenous malformations rarely present with pulmonary hypertension. We report the case of a 3-month-old boy who developed severe pulmonary hypertension due to a hepatic arteriovenous malformation. The use of pulmonary vasodi
Externí odkaz:
https://doaj.org/article/19d22f7633f34bf8bfbf48cbb4ef9663
Autor:
Ryo Shirotsuki, Kazuo Oshima, Kosuke Chiba, Takahisa Tainaka, Akinari Hinoki, Yujiro Tanaka, Naruhiko Murase, Wataru Sumida, Hiroo Uchida, Chiyoe Shirota
Publikováno v:
Pediatric Surgery International. 34(10):1087-1092
Purpose: We previously showed that meticulous probing and resection of the intrahepatic bile duct stenosis (IHBDS)-causing membrane or septum was effective in preventing hepatolithiasis after choledochal cyst excisions in open surgeries. Then, we int
Autor:
Kosuke Chiba, Hiroo Uchida, Toshiki Nakane, Yujiro Tanaka, Naruhiko Murase, Takahisa Tainaka, Chiyoe Shirota, Ryo Shirotsuki, Kazuo Oshima, Wataru Sumida, Akinari Hinoki
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-5 (2018)
BMC Pediatrics
BMC Pediatrics
Background Emergency rescue lung resection is rarely performed to treat congenital lung cysts (CLCs) in neonates. Many reports have described fetal CLC treatment; however, prenatal predictors for postnatal respiratory failure have not been characteri
Autor:
Akihide Tanano, Akinari Hinoki, Kazuki Yokota, Kazuo Oshima, Naruhiko Murase, Kosuke Chiba, Hiroo Uchida, Ryo Shirotsuki, Takahisa Tainaka, Hiroshi Kawashima, Chiyoe Shirota, Yujiro Tanaka, Hizuru Amano
Publikováno v:
Journal of Laparoendoscopic & Advanced Surgical Techniques. 27:71-75
Background: The treatment of long-gap esophageal atresia remains an issue for pediatric surgeons. Many techniques for treating long-gap esophageal atresia have been proposed, but the optimal method has not been established. The thoracoscopic esophage
Autor:
Kazuo Oshima, Hiroo Uchida, Akinari Hinoki, Ryo Shirotsuki, Hisami Ando, Takahisa Tainaka, Kazuki Yokota, Yasuyuki Ono, Chiyoe Shirota, Naruhiko Murase
Publikováno v:
Journal of Hepato-Biliary-Pancreatic Sciences. 23:715-720
Background The indications for and efficacy of revision of portoenterostomy (PE) for biliary atresia (BA) needs to be reassessed in an era of liver transplantation. We therefore reviewed the long-term outcomes following revision of PE. Methods This w
Autor:
Yujiro Tanaka, Masataka Takahashi, Kazuo Oshima, Takahisa Tainaka, Kosuke Chiba, Yuji Morimoto, Hiroo Uchida, Chiyoe Shirota, Wataru Sumida, Akinari Hinoki, Ryo Shirotsuki, Naruhiko Murase
Publikováno v:
The American Journal of Case Reports
Patient: Male, 15 Final Diagnosis: Lymphatic malformations Symptoms: Abdominal pain Medication: — Clinical Procedure: Navigation surgery Specialty: Surgery Objective: Unusual or unexpected effect of treatment Background: We used indocyanine green (
Autor:
Chiyoe Shirota, Hiroo Uchida, Kazuki Yokota, Akihide Tanano, Ryo Shirotsuki, Naruhiko Murase, Takahisa Tainaka, Yasuyuki Ono
Publikováno v:
BioMed Research International, Vol 2015 (2015)
BioMed Research International
BioMed Research International
Purpose.Kasai portoenterostomy is the standard therapy for biliary atresia (BA). If Kasai is unsuccessful, there is controversy over whether revision of Kasai restores adequate biliary drainage. Although there are several reports of laparoscopic Kasa