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Journal of Human Genetics|March 4, 2016
Clinical manifestations and growth of patients with urea cycle disorders in JapanKimitoshi Nakamura, Jun Kido, Shirou Matsumoto, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|June 6, 2015
Idiopathic disseminated bacillus Calmette-Guerin infection in three infantsJun Kido, Tomoyuki Mizukami, Osamu Ohara, et al.Metabolic Brain Disease|June 28, 2018
Early liver transplantation in neonatal-onset and moderate urea cycle disorders may lead to normal neurodevelopmentJun Kido, Shirou Matsumoto, Hiroshi Mitsubuchi, et al.American Journal of Medical Genetics. Part A|April 14, 2021
Variants associated with urea cycle disorders in Japanese patients: Nationwide study and literature reviewJun Kido, Shirou Matsumoto, Keishin Sugawara, et al.Molecular Genetics and Metabolism Reports|September 16, 2024
Rapid genotyping of inversion variants in Mucopolysaccharidosis type II using long-range PCR: A case reportYusuke Hattori, Jun Kido, Keishin Sugawara, et al.Journal of Human Genetics|May 22, 2019
Urea cycle disorders-updateShirou Matsumoto, Johannes Häberle, Jun Kido, et al.Molecular Genetics and Metabolism|May 18, 2026
Riboflavin-responsive hyperprolinemia type I with a PRODH p.Thr466Met variant: Clinical and fibroblast-based evidenceJun Kido, Keishin Sugawara, Ikuko Egashira, et al.Pediatric Transplantation|October 29, 2018
Recovery of severe acute liver failure without transplantation in patients with Wilson diseaseJun Kido, Shirou Matsumoto, Rieko Sakamoto, et al.Human Genome Variation|June 7, 2017
Clinical manifestations in two patients with pyruvate dehydrogenase deficiency and long-term survivalTakanobu Yoshida, Jun Kido, Hiroshi Mitsubuchi, et al.Case Reports in Neurology|October 21, 2020
Effect of Flunarizine on Alternating Hemiplegia of Childhood in a Patient with the p.E815K Mutation in ATP1A3: A Case ReportShouichirou Kusunoki, Jun Kido, Ken Momosaki, et al.Pageof 9