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Triple A syndrome in Japan.
Ikeda M, Hirano M, Shinoda K, Katsumata N, Furutama D, Nakamura K, Ikeda S, Tanaka T, Hanafusa T, Kitajima H, Kohno H, Nakagawa M, Nakamura Y, Ueno S. Ikeda M, et al. Among authors: nakamura y, nakamura k. Muscle Nerve. 2013 Sep;48(3):381-6. doi: 10.1002/mus.23770. Epub 2013 Jul 17. Muscle Nerve. 2013. PMID: 23861206
The First Nationwide Survey and Genetic Analyses of Bardet-Biedl Syndrome in Japan.
Hirano M, Satake W, Ihara K, Tsuge I, Kondo S, Saida K, Betsui H, Okubo K, Sakamoto H, Ueno S, Ikuno Y, Ishihara R, Iwahashi H, Ohishi M, Mano T, Yamashita T, Suzuki Y, Nakamura Y, Kusunoki S, Toda T. Hirano M, et al. Among authors: nakamura y. PLoS One. 2015 Sep 1;10(9):e0136317. doi: 10.1371/journal.pone.0136317. eCollection 2015. PLoS One. 2015. PMID: 26325687 Free PMC article.
Multiple system involvement in a Japanese patient with a V31A mutation in the SOD1 gene.
Sakamoto H, Akamatsu M, Hirano M, Saigoh K, Ueno S, Isono C, Kusunoki S, Nakamura Y. Sakamoto H, et al. Among authors: nakamura y. Amyotroph Lateral Scler Frontotemporal Degener. 2014 Jun;15(3-4):312-4. doi: 10.3109/21678421.2013.873051. Epub 2014 Mar 10. Amyotroph Lateral Scler Frontotemporal Degener. 2014. PMID: 24611504
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