Showing 1 - 13 results of 13 for search 'Keishin Sugawara', query time: 0.04s
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High-Risk Screening for Fabry Disease: A Nationwide Study in Japan and Literature Review by Takaaki Sawada, Jun Kido, Keishin Sugawara, Kimitoshi Nakamura
Published 2021-09-01
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Hyperprolinemia type I caused by homozygous p.T466M mutation in PRODH by Rina Hama, Jun Kido, Keishin Sugawara, Toshiro Nakamura, Kimitoshi Nakamura
Published 2021-07-01
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Gene therapy for lysosomal storage diseases: Current clinical trial prospects by Jun Kido, Jun Kido, Keishin Sugawara, Kimitoshi Nakamura, Kimitoshi Nakamura
Published 2023-01-01
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Detection of novel Fabry disease‐associated pathogenic variants in Japanese patients by newborn and high‐risk screening by Takaaki Sawada, Jun Kido, Keishin Sugawara, Shirou Matsumoto, Fumio Takada, Kazuya Tsuboi, Akira Ohtake, Fumio Endo, Kimitoshi Nakamura
Published 2020-11-01
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Pathogenic variants of ornithine transcarbamylase deficiency: Nation-wide study in Japan and literature review by Jun Kido, Jun Kido, Keishin Sugawara, Takaaki Sawada, Takaaki Sawada, Shirou Matsumoto, Shirou Matsumoto, Kimitoshi Nakamura, Kimitoshi Nakamura
Published 2022-10-01
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Frequency of iduronate-2-sulfatase gene variants detected in newborn screening for mucopolysaccharidosis type II in Japan by Yusuke Hattori, Takaaki Sawada, Jun Kido, Keishin Sugawara, Shinichiro Yoshida, Shirou Matsumoto, Takahito Inoue, Shinichi Hirose, Kimitoshi Nakamura
Published 2023-12-01
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Newborn screening for Fabry disease in the western region of Japan by Takaaki Sawada, Jun Kido, Shinichiro Yoshida, Keishin Sugawara, Ken Momosaki, Takahito Inoue, Go Tajima, Hirotake Sawada, Shirou Mastumoto, Fumio Endo, Shinichi Hirose, Kimitoshi Nakamura
Published 2020-03-01
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