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[Congenital muscular dystrophy and alpha-dystroglycanopathy].
Saito F, Matsumura K, Hagiwara H, Shimizu T. Saito F, et al. Among authors: hagiwara h. Rinsho Shinkeigaku. 2008 Aug;48(8):543-9. doi: 10.5692/clinicalneurol.48.543. Rinsho Shinkeigaku. 2008. PMID: 18939472 Review. Japanese.
Secretion of N-terminal domain of α-dystroglycan in cerebrospinal fluid.
Saito F, Saito-Arai Y, Nakamura-Okuma A, Ikeda M, Hagiwara H, Masaki T, Shimizu T, Matsumura K. Saito F, et al. Among authors: hagiwara h. Biochem Biophys Res Commun. 2011 Jul 29;411(2):365-9. doi: 10.1016/j.bbrc.2011.06.150. Epub 2011 Jun 29. Biochem Biophys Res Commun. 2011. PMID: 21741360
Unexpected Mutations by CRISPR-Cas9 CTG Repeat Excision in Myotonic Dystrophy and Use of CRISPR Interference as an Alternative Approach.
Ikeda M, Taniguchi-Ikeda M, Kato T, Shinkai Y, Tanaka S, Hagiwara H, Sasaki N, Masaki T, Matsumura K, Sonoo M, Kurahashi H, Saito F. Ikeda M, et al. Among authors: hagiwara h. Mol Ther Methods Clin Dev. 2020 May 22;18:131-144. doi: 10.1016/j.omtm.2020.05.024. eCollection 2020 Sep 11. Mol Ther Methods Clin Dev. 2020. PMID: 32637445 Free PMC article.
[Collier's sign in Miller Fisher syndrome].
Miyaishi M, Hemmi S, Hagiwara H, Murakami T, Sunada Y. Miyaishi M, et al. Among authors: hagiwara h. Rinsho Shinkeigaku. 2006 Oct;46(10):712-4. Rinsho Shinkeigaku. 2006. PMID: 17323781 Japanese.
741 results