Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Seika Kuroda"'
Autor:
Yoichiro Tada, Junpei Orihara, Yamato Wada, Ei Uchinaka, Tomohiro Osaki, Keigo Ashida, Shigeru Tatebe, Seika Kuroda, Yasuaki Hirooka
Publikováno v:
Surgical Case Reports, Vol 8, Iss 1, Pp 1-5 (2022)
Abstract Background Internal hernias are formed by the protrusion of internal organs through an aperture formed congenitally or postoperatively. Internal hernias are most commonly associated with the small intestine. Only two cases of a post-sigmoid
Externí odkaz:
https://doaj.org/article/6c2be2bf0ec44db5afb926b352fcc5ec
Publikováno v:
Surgical Case Reports, Vol 7, Iss 1, Pp 1-5 (2021)
Abstract Background Congenital pyloric atresia (CPA) is a rare gastrointestinal anomaly frequently associated with epidermolysis bullosa (EB). Although the complications of familial isolated CPA are minor, delays in diagnosis can increase the chances
Externí odkaz:
https://doaj.org/article/2d592b19af9c4642b9b1ace429dce3fb
Autor:
Kazunori Masahata, Toshimichi Hasegawa, Seika Kuroda, Nobumasa Takahashi, Ikuko Nojima, Noriko Kimura, Keiji Tsuchimoto, Akio Kubota
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 3, Iss 9, Pp 389-391 (2015)
Pure esophageal atresia is typically characterized by a long gap between the upper and lower pouches, with a gasless abdomen and no fistula. The association of pure esophageal atresia with an atretic segment is extremely rare. We report a rare varian
Externí odkaz:
https://doaj.org/article/a0cebe33d51a439a9bbe9ad63de1c1aa
Publikováno v:
Surgical Case Reports
Surgical Case Reports, Vol 7, Iss 1, Pp 1-5 (2021)
Surgical Case Reports, Vol 7, Iss 1, Pp 1-5 (2021)
Background Congenital pyloric atresia (CPA) is a rare gastrointestinal anomaly frequently associated with epidermolysis bullosa (EB). Although the complications of familial isolated CPA are minor, delays in diagnosis can increase the chances of morbi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ab8616bb15787d059ad8def5e756dd7
https://doi.org/10.1186/s40792-020-01096-1
https://doi.org/10.1186/s40792-020-01096-1
Publikováno v:
Journal of Urology. 178:1650-1653
Familial clustering of vesicoureteral reflux suggests that genetic factors have an important role in the pathogenesis of vesicoureteral reflux. Transforming growth factor-beta1 is a multifunctional peptide that controls proliferation and differentiat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08ba41882cb8ee0a99d2545db93864d0
https://doi.org/10.1016/j.juro.2007.03.199
https://doi.org/10.1016/j.juro.2007.03.199
Autor:
Prem Puri, Seika Kuroda
Publikováno v:
Pediatric Surgery International. 23:441-445
Vesico-ureteral reflux (VUR) is the most common inherited disorder of the lower urinary tract. Children with VUR are at risk for ongoing renal damage with subsequent infections. IL8 is an important inflammatory mediator which can be produced by epith
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71fc3128cc6abab40a381d61af319925
https://doi.org/10.1007/s00383-006-1857-7
https://doi.org/10.1007/s00383-006-1857-7
Autor:
Takashi Sasaki, Seika Kuroda, Etani Yuri, Toshimichi Hasegawa, Hideki Soh, Kaname Tomoda, Masahiro Fukuzawa, Takuya Kimura
Publikováno v:
Surgical Laparoscopy, Endoscopy & Percutaneous Techniques. :285-288
Congenital portosystemic shunt is a rare clinical entity that may progress to jaundice, severe encephalopathy, and pulmonary hypertension and require surgical correction or coil embolization. We present a novel approach to the management of children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::931574d9347d565f2c601dfed8d373c4
https://doi.org/10.1097/00129689-200410000-00012
https://doi.org/10.1097/00129689-200410000-00012
Publikováno v:
Genes, Chromosomes and Cancer. 40:133-139
We describe a neonate who had a rare tumor combination of a malignant rhabdoid tumor of the kidney (MRTK) and a brain primitive neuroectodermal tumor (PNET). Genetic alterations of the SNF5/INI1/SMARCB1 gene were investigated by PCR–single-strand c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afdfa74fb67d4ffde10e2b9d98b01abb
https://doi.org/10.1002/gcc.20026
https://doi.org/10.1002/gcc.20026
Publikováno v:
The journal of the Japanese Practical Surgeon Society. 58:1126-1129
Herniography was performed to improve diagnosis prior to surgery in a 9-year-old male patient, who presented a left groin bulging mass not typical for indirect hernia. Under local anesthesia, peritoneal needle-puncture was performed with ultrasonogra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d95e1d094c3397afd27935e23fb19bfe
https://doi.org/10.3919/ringe1963.58.1126
https://doi.org/10.3919/ringe1963.58.1126
Autor:
Seika Kuroda, Masaaki Nakahara, Kenjirou Fukuhara, Takashi Emoto, Kazuyasu Nakao, Nobuo Ogino, Satoru Miyazaki, Toshirou Nishida, Masahiko Tsujimoto, Katsuaki Maeda
Publikováno v:
The journal of the Japanese Practical Surgeon Society. 56:81-85
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88fc3771f3e93a908d5471b2920566f1
https://doi.org/10.3919/ringe1963.56.81
https://doi.org/10.3919/ringe1963.56.81