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151. Myb-related Schizosaccharomyces pombe cdc5p is structurally and functionally conserved in eukaryotes.

152. Nitric oxide in hepatopulmonary syndrome.

153. Detection of the PGP9.5 and tyrosine hydroxylase mRNAs for minimal residual neuroblastoma cells in bone marrow and peripheral blood.

154. Peripheral blood stem cell transplantation for hepatoblastoma with microscopical residue: a therapeutic approach for incompletely resected tumor.

155. [TNM classification--pediatric tumors].

156. Surgical treatment of biliary atresia in the liver transplantation era.

157. Disorder of bile acid metabolism in children with short bowel syndrome.

158. Abnormal distribution of nerve fibers in the liver of biliary atresia.

159. Assessment of nutritional status of postoperative patients with biliary atresia.

160. Clinical significance of 99mTc-DTPA galactosyl human serum albumin scintigram in follow-up after Kasai operation.

161. The outcome of surgery for biliary atresia and the current status of long-term survivors.

162. Living related partial liver transplantation in biliary atresia: 11 cases of experience.

163. Japanese Biliary Atresia Registry, 1989 to 1994.

164. [Long-term outcome of surgery for biliary atresia].

165. The structure of the transitional and aganglionic zones of Auerbach's plexus in patients with Hirschsprung's disease: a computer-assisted three-dimensional reconstruction study.

166. Current status of 21 patients who have survived more than 20 years since undergoing surgery for biliary atresia.

168. [Familial neuroblastoma].

169. Right pneumonectomy syndrome: report of two cases.

170. The effect of hepatic portal dissection on the portal vein structure in biliary atresia.

171. Pituitary adenylate cyclase activating polypeptide (PACAP)-like immunoreactivity in ganglioneuroblastoma and neuroblastoma.

172. Bannayan-Zonana syndrome associated with lipomas, hemangiomas, and lymphangiomas.

173. Hepatocellular carcinoma in children with hepatitis B surface antigen.

174. Biliary atresia.

175. [Scintigraphic assessment of the intestinal absorptive capacity].

176. Proposal and assessment of Japanese tumor node metastasis postsurgical histopathological staging system for neuroblastoma based on an analysis of 495 cases.

177. Significance of plasma neuropeptide Y (NPY) in diagnosis and prognosis of neuroblastoma.

178. Two cases of bizarre rib anomalies associated with intestinal malformation.

179. [Present status of neuroblastoma mass screening in Japan. Neuroblastoma-Committee of the Japanese Childhood Cancer Society].

180. Postoperative gastrointestinal hemorrhage in biliary atresia.

181. Surgical treatment of congenital dilatation of the bile duct with special reference to late complications after total excisional operation.

182. Immunocytochemical characterization of supporting cells in the enteric nervous system in Hirschsprung's disease.

183. Two-point rectal mucosal biopsy for selection of surgical treatment of Hirschsprung's disease.

184. Long-term follow-up after surgery for patients with biliary atresia.

185. Burkitt's lymphoma cell line bearing surface IgA and negative for nuclear antigen of Epstein-Barr virus (EBNA).

186. [Histochemical diagnosis of Hirschsprung's disease and 2 point rectal mucosal biopsies for selection of surgical treatment].

187. Changes of portal vein pressure and intrahepatic blood vessels after surgery for biliary atresia.

188. Acrodermatitis enteropathica-like eruption association with parenteral nutrition.

189. Follow-up studies of long term survivors after hepatic portoenterostomy for "noncorrectible" biliary atresia.

190. Studies on the changes of serum bilirubin level after surgery in biliary atresia.

191. Surgical limitation for biliary atresia: indication for liver transplantation.

192. In biliary atresia duct histology correlates with bile flow.

193. Postoperative changes of intrahepatic portal veins in biliary atresia--a 3-D reconstruction study.

194. A patient with biliary atresia who died 28 years after hepatic portojejunostomy.

195. Portal hypertension after successful hepatic portoenterostomy in biliary atresia.

196. [Nutritional condition and absorptive capacity of 14 infants with short bowel syndrome].

197. Operative procedures for choledochal cyst.

198. [The evaluation of the nutritional condition and the absorptive capacity in long-term follow-up of infants with short bowel syndrome].

200. Persistent jaundice after hepatic porto-jejunostomy in biliary atresia: are the patients' prognoses determined within 3 months after surgery?

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