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Department Of Pediatric General And Urogenital Surgery Juntendo University | 論文
- Disseminated mixed intestinal dysmotility(DMID) : a new intestinal ganglion cell disorder?
- P-449 Intraoperative colonoscopy facilitates safe dissection of the distal rectal pouch in male high/intermediate type imperforate anus patients without rectourethral fistula
- P-128 Lower morbidity due to incarceration in inguinal hernia when followed-up by pediatric surgeons
- Spontaneous sutureless closure of the abdominal wall defect in gastroschisis using a commercial wound retractor system
- Radiographic signs predictive of success of hydrostatic reduction of intussusception
- Immature enteric neurons in Ncx/Hox11L.1 deficient intestinal neuronal dysplasia model mice
- P-453 Retroperitoneoscopic adhesiolysis: renovascular ureteropelvic junction obstruction : A case report
- P-29 Left hepatic lobectomy in a long-term biliary atresia survivor
- P-452 Bilateral duplex kidney associated with the urogenital sinus and four megaureters : A case report
- P-450 Comparing clinical assessment protocols for postoperative fecal continence in imperforate anus
- P-292 Serpentine-like syndrome (brachioesophagus, intrathoracic stomach, rachischisis) : A case report
- P-290 Thoracoscopic plication for diaphragmatic eventration in a neonate
- P-289 Late-presenting congenital diaphragmatic hernia requiring emergency surgery : report of 3 cases
- P-30 Modified balloon occluded retrograde obliteration for postoperative intestinal varices in biliary atresia : a case repor
- Collis-Nissen fundoplication using a computer-powered right angle linear cutting stapler in children
- Complete resection of hepatoblastoma originating in the caudate lobe : case report and literature review
- Treves' field pouch hernia : our experience and literature review
- Immunological investigation of the hepatic tissue from infants with biliary atresia
- Contralateral pleural recurrence of adrenocortical carcinoma after surgical resection
- Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson's disease