Saito K - Search Results

1

Charcot-Marie-Tooth disease type 4C in Japan: report of a case.

Iguchi M, Hashiguchi A, Ito E, Toda K, Urano M, Shimizu Y, Takeuchi C, Saito K, Takashima H, Uchiyama S. Iguchi M, et al. Among authors: saito k. Muscle Nerve. 2013 Feb;47(2):283-6. doi: 10.1002/mus.23540. Epub 2012 Dec 28. Muscle Nerve. 2013. PMID: 23281072

2

Clinical and mutational spectrum of Japanese patients with recessive variants in SH3TC2.

Yuan JH, Hashiguchi A, Okamoto Y, Yoshimura A, Ando M, Shiomi K, Saito K, Takahashi M, Ichinose K, Ohmichi T, Ichikawa K, Tadashi A, Takigawa H, Shibayama H, Takashima H. Yuan JH, et al. Among authors: saito k. J Hum Genet. 2018 Mar;63(3):281-287. doi: 10.1038/s10038-017-0388-5. Epub 2018 Jan 10. J Hum Genet. 2018. PMID: 29321516

3

[Gene mutation and genetic counseling].

Matsuo M, Urano M, Saito K. Matsuo M, et al. Among authors: saito k. Nihon Rinsho. 2009 Jun;67(6):1191-6. Nihon Rinsho. 2009. PMID: 19507513 Japanese.

4

Epidemiological investigation of spinal muscular atrophy in Japan.

Ito M, Yamauchi A, Urano M, Kato T, Matsuo M, Nakashima K, Saito K. Ito M, et al. Among authors: saito k. Brain Dev. 2022 Jan;44(1):2-16. doi: 10.1016/j.braindev.2021.08.002. Epub 2021 Aug 25. Brain Dev. 2022. PMID: 34452804

5

Corticosteroid therapy for duchenne muscular dystrophy: improvement of psychomotor function.

Sato Y, Yamauchi A, Urano M, Kondo E, Saito K. Sato Y, et al. Among authors: saito k. Pediatr Neurol. 2014 Jan;50(1):31-7. doi: 10.1016/j.pediatrneurol.2013.07.022. Epub 2013 Oct 15. Pediatr Neurol. 2014. PMID: 24138948

6

Target resequencing of neuromuscular disease-related genes using next-generation sequencing for patients with undiagnosed early-onset neuromuscular disorders.

Kitamura Y, Kondo E, Urano M, Aoki R, Saito K. Kitamura Y, et al. Among authors: saito k. J Hum Genet. 2016 Nov;61(11):931-942. doi: 10.1038/jhg.2016.79. Epub 2016 Jun 30. J Hum Genet. 2016. PMID: 27357428

7

Genetic Counseling for Couples Seeking Noninvasive Prenatal Testing in Japan: Experiences of Pregnant Women and their Partners.

Watanabe M, Matsuo M, Ogawa M, Uchiyama T, Shimizu S, Iwasaki N, Yamauchi A, Urano M, Numabe H, Saito K. Watanabe M, et al. Among authors: saito k. J Genet Couns. 2017 Jun;26(3):628-639. doi: 10.1007/s10897-016-0038-7. Epub 2016 Nov 9. J Genet Couns. 2017. PMID: 27830353

8

Relationships between long-term observations of motor milestones and genotype analysis results in childhood-onset Japanese spinal muscular atrophy patients.

Kaneko K, Arakawa R, Urano M, Aoki R, Saito K. Kaneko K, et al. Among authors: saito k. Brain Dev. 2017 Oct;39(9):763-773. doi: 10.1016/j.braindev.2017.04.018. Epub 2017 Jun 7. Brain Dev. 2017. PMID: 28601407

9

Analysis of spinal muscular atrophy-like patients by targeted resequencing.

Hosokawa S, Kubo Y, Arakawa R, Takashima H, Saito K. Hosokawa S, et al. Among authors: saito k. Brain Dev. 2020 Feb;42(2):148-156. doi: 10.1016/j.braindev.2019.10.008. Epub 2019 Nov 14. Brain Dev. 2020. PMID: 31734026

10

Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation.

Seki A, Ishikawa T, Daumy X, Mishima H, Barc J, Sasaki R, Nishii K, Saito K, Urano M, Ohno S, Otsuki S, Kimoto H, Baruteau AE, Thollet A, Fouchard S, Bonnaud S, Parent P, Shibata Y, Perrin JP, Le Marec H, Hagiwara N, Mercier S, Horie M, Probst V, Yoshiura KI, Redon R, Schott JJ, Makita N. Seki A, et al. Among authors: saito k. J Am Coll Cardiol. 2017 Jul 18;70(3):358-370. doi: 10.1016/j.jacc.2017.05.039. J Am Coll Cardiol. 2017. PMID: 28705318 Free article.

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