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A MinION-based Long-Read Sequencing Application With One-Step PCR for the Genetic Diagnosis of 21-Hydroxylase Deficiency.
Adachi E, Nakagawa R, Tsuji-Hosokawa A, Gau M, Kirino S, Yogi A, Nakatani H, Takasawa K, Yamaguchi T, Kosho T, Murakami M, Tajima T, Hasegawa T, Yamada T, Morio T, Ohara O, Kashimada K. Adachi E, et al. Among authors: nakagawa r. J Clin Endocrinol Metab. 2024 Feb 20;109(3):750-760. doi: 10.1210/clinem/dgad577. J Clin Endocrinol Metab. 2024. PMID: 37804107
Cause of acute encephalitis/encephalopathy in Japanese children diagnosed by a rapid and comprehensive virological detection system and differences in their clinical presentations.
Takasawa K, Nakagawa R, Takishima S, Moriyama K, Watanabe K, Kiyohara K, Hasegawa T, Shimohira M, Kashimada K, Shimizu N, Morio T. Takasawa K, et al. Among authors: nakagawa r. Brain Dev. 2018 Feb;40(2):107-115. doi: 10.1016/j.braindev.2017.07.014. Epub 2017 Aug 8. Brain Dev. 2018. PMID: 28801087
589 results