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Survey of patients with spinal muscular atrophy on the island of Shikoku, Japan.
Okamoto K, Motoki T, Saito I, Urate R, Aibara K, Jogamoto T, Fukuda M, Wakamoto H, Maniwa S, Kondo Y, Toda Y, Goji A, Mori T, Soga T, Konishi Y, Nagai S, Takami Y, Tokorodani C, Nishiuchi R, Usui D, Ando R, Tada S, Yamanishi Y, Nagai M, Arakawa R, Saito K, Nishio H, Ishii E, Eguchi M. Okamoto K, et al. Among authors: saito k, saito i. Brain Dev. 2020 Sep;42(8):594-602. doi: 10.1016/j.braindev.2020.05.004. Epub 2020 Jun 3. Brain Dev. 2020. PMID: 32505480
Human first-trimester chorionic villi have a myogenic potential.
Arakawa R, Aoki R, Arakawa M, Saito K. Arakawa R, et al. Among authors: saito k. Cell Tissue Res. 2012 Apr;348(1):189-97. doi: 10.1007/s00441-012-1340-9. Epub 2012 Feb 28. Cell Tissue Res. 2012. PMID: 22370594 Free PMC article.
[A case of spinal muscular atrophy type 0 in Japan].
Okamoto K, Saito K, Sato T, Ishigaki K, Funatsuka M, Osawa M. Okamoto K, et al. Among authors: saito k. No To Hattatsu. 2012 Sep;44(5):387-91. No To Hattatsu. 2012. PMID: 23012868 Japanese.
Spinal muscular atrophy: from gene discovery to clinical trials.
Nurputra DK, Lai PS, Harahap NI, Morikawa S, Yamamoto T, Nishimura N, Kubo Y, Takeuchi A, Saito T, Takeshima Y, Tohyama Y, Tay SK, Low PS, Saito K, Nishio H. Nurputra DK, et al. Among authors: saito k, saito t. Ann Hum Genet. 2013 Sep;77(5):435-63. doi: 10.1111/ahg.12031. Epub 2013 Jul 23. Ann Hum Genet. 2013. PMID: 23879295 Review.
Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patients.
Yamamoto T, Sato H, Lai PS, Nurputra DK, Harahap NI, Morikawa S, Nishimura N, Kurashige T, Ohshita T, Nakajima H, Yamada H, Nishida Y, Toda S, Takanashi J, Takeuchi A, Tohyama Y, Kubo Y, Saito K, Takeshima Y, Matsuo M, Nishio H. Yamamoto T, et al. Among authors: saito k. Brain Dev. 2014 Nov;36(10):914-20. doi: 10.1016/j.braindev.2013.11.009. Epub 2013 Dec 17. Brain Dev. 2014. PMID: 24359787
8,922 results