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Hemodialysis International. International Symposium on Home Hemodialysis|November 3, 2016
Pulmonary artery hypertension in methylmalonic acidemiaJun Kido, Hiroshi Mitsubuchi, Mina Sakanashi, et al.World Journal of Hepatology|March 16, 2017
Hyperammonemia crisis following parturition in a female patient with ornithine transcarbamylase deficiencyJun Kido, Tatsuya Kawasaki, Hiroshi Mitsubuchi, et al.Case Reports in Neurology|October 15, 2019
The Effect of S-Adenosylmethionine Treatment on Neurobehavioral Phenotypes in Lesch-Nyhan Disease: A Case ReportKen Momosaki, Jun Kido, Shiro Matsumoto, et al.Clinical Laboratory|February 27, 2018
A Significant Difference in the Blood Carnitine Values Obtained by the Enzymatic Cycling and Tandem Mass Spectrometry MethodsJun Kido, Hironobu Inoue, Yosuke Suzuki, et al.Orphanet Journal of Rare Diseases|August 27, 2020
Fabry disease screening in high-risk populations in Japan: a nationwide studyShinichiro Yoshida, Jun Kido, Takaaki Sawada, et al.JBMR Plus|February 10, 2025
Newborn screening for hypophosphatasia: development of a high-throughput tissue nonspecific alkaline phosphatase activity assay using dried blood spotsYusuke Noda, Jun Kido, Takaaki Sawada, et al.Molecular Genetics and Metabolism Reports|December 6, 2023
Frequency of iduronate-2-sulfatase gene variants detected in newborn screening for mucopolysaccharidosis type II in JapanYusuke Hattori, Takaaki Sawada, Jun Kido, et al.Clinical Case Reports|September 11, 2023
Heterozygous c.175C>T variant in PURA gene causes severe developmental delayYusuke Noda, Jun Kido, Yohei Misumi, et al.Journal of Human Genetics|April 1, 2018
High-risk screening for Gaucher disease in patients with neurological symptomsKen Momosaki, Jun Kido, Shirou Matsumoto, et al.Human Genome Variation|March 14, 2026
Non-pterygium Escobar syndrome from compound-heterozygous CHRNG variants: genotype-phenotype insightsJun Kido, Hiroe Ueno, Yohei Misumi, et al.Pageof 9