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Investigative Ophthalmology & Visual Science|August 31, 2001
Mutation of human retinal fascin gene (FSCN2) causes autosomal dominant retinitis pigmentosaY Wada, T Abe, T Takeshita, et al.
American Journal of Ophthalmology|October 9, 2001
A novel (Pro79Thr) mutation in the FKHL7 gene in a Japanese family with Axenfeld-Rieger syndromeT Suzuki, K Takahashi, S Kuwahara, et al.
Hinyokika Kiyo. Acta Urologica Japonica|December 14, 2018
[Urinary Retention Caused by Necrotic Tissues in the Bladder of a Female Recipient of a Living-Donor Kidney Transplant : A Case Report]Yuki Muranishi, Nobuyuki Fukuzawa, Yoshiki Wada, et al.
Gan to Kagaku Ryoho. Cancer & Chemotherapy|March 1, 1994
[Late phase II study of CGS16949A, a new aromatase inhibitor--a multicentral cooperative study (Western Japan Group)]T Wada, Y Nomura, Y Oohashi, et al.
The Pediatric Infectious Disease Journal|October 2, 2020
Clostridium tertium Peritonitis and Bacteremia in a Neonate With Congenital Intestinal Atresia: A Case ReportKazue Morikawa, Masatoshi Nozaki, Katsuya Hirata, et al.
Scientific Reports|March 3, 2019
Glycemic control and survival in peritoneal dialysis patients with diabetes: A 2-year nationwide cohort studyMasanori Abe, Takayuki Hamano, Junichi Hoshino, et al.
International Journal of Surgery Case Reports|August 20, 2025
Intrathoracic anastomotic leak after esophagojejunostomy in a patient with preoperative coronavirus disease 2019: A case treated with T-tube drainageTakuma Kurotaki, Yuma Ebihara, Hirotake Abe, et al.
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