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International Journal of Neonatal Screening|October 19, 2020
Newborn Screening for Pompe DiseaseTakaaki Sawada, Jun Kido, Kimitoshi NakamuraDiagnostics (Basel, Switzerland)|October 23, 2021
High-Risk Screening for Fabry Disease: A Nationwide Study in Japan and Literature ReviewTakaaki Sawada, Jun Kido, Keishin Sugawara, et al.Hemodialysis International. International Symposium on Home Hemodialysis|September 3, 2019
Rhabdomyolysis in organic acidemia patients manifesting with metabolic decompensationJun Kido, Shirou Matsumoto, Takaaki Sawada, et al.Frontiers in Genetics|October 28, 2022
Pathogenic variants of ornithine transcarbamylase deficiency: Nation-wide study in Japan and literature reviewJun Kido, Keishin Sugawara, Takaaki Sawada, 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.Clinical and Experimental Nephrology|December 27, 2022
High-risk screening for Fabry disease in hemodialysis patients in Chiba Prefecture, JapanToshiyuki Imasawa, Kei Murayama, Takaaki Sawada, 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.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.Molecular Genetics and Metabolism Reports|June 22, 2026
Newborn screening for Fabry disease in Japan: an additional 3-year reportTakaaki Sawada, Jun Kido, Keishin Sugawara, et al.Molecular Genetics and Metabolism|April 23, 2025
Newborn screening for spinal muscular atrophy: The potential of digital polymerase chain reaction techniqueJun Kido, Ken Haruno, Keishin Sugawara, et al.Pageof 3