Showing results (1-10 of 9) with videos related to
Sort By:
Pageof 1
Clinical and Experimental Nephrology|December 17, 2008
Steroid-sensitive nephrotic syndrome in two familiesOsamu Motoyama, Hidenori Sugawara, Michihiro Hatano, et al.Scandinavian Journal of Urology and Nephrology|March 8, 2003
Effects of leukocytosis and macrophage activation on anti-Thy 1.1 glomerulonephritis in the ratAkihiro Futamura, Kiyoshi Izumino, Hidenori Sugawara, et al.Journal of Diabetes Investigation|November 21, 2014
Comparison of brachial artery flow-mediated dilation in youth with type 1 and type 2 diabetes mellitusKoji Ohsugi, Hidenori Sugawara, Kanako Ebina, et al.Clinical Journal of Gastroenterology|September 13, 2021
A case of child-to-father transmission of hepatitis B virus in Japan: a rare infection routeHidenori Sugawara, Yoshiko Nakayama, Sawako Kato, et al.Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|August 18, 2010
Does the spread of hepatitis B virus genotype A increase the risk of intrafamilial transmission in Japan?Haruki Komatsu, Hidenori Sugawara, Ayano Inui, et al.The Tohoku Journal of Experimental Medicine|May 29, 2015
Phenotypic Variability and Newly Identified Mutations of the IVD Gene in Japanese Patients with Isovaleric AcidemiaOsamu Sakamoto, Natsuko Arai-Ichinoi, Hiroshi Mitsubuchi, et al.Pediatric Diabetes|September 30, 2016
Molecular and clinical features of KATP -channel neonatal diabetes mellitus in JapanYukiko Hashimoto, Sumito Dateki, Masakazu Hirose, et al.Brain & Development|September 19, 2013
Urine screening for patients with developmental disabilities detected a patient with creatine transporter deficiency due to a novel missense mutation in SLC6A8Hidekazu Kato, Fuyu Miyake, Hiroko Shimbo, et al.The Journal of Clinical Endocrinology and Metabolism|September 11, 2019
Genetics of Congenital Isolated TSH Deficiency: Mutation Screening of the Known Causative Genes and a Literature ReviewChiho Sugisawa, Tetsuya Takamizawa, Kiyomi Abe, et al.Pageof 1