Saito T - Search Results

1

Trinucleotide insertion in the SMN2 promoter may not be related to the clinical phenotype of SMA.

Harahap NI, Takeuchi A, Yusoff S, Tominaga K, Okinaga T, Kitai Y, Takarada T, Kubo Y, Saito K, Sa'adah N, Nurputra DK, Nishimura N, Saito T, Nishio H. Harahap NI, et al. Among authors: saito k, saito t. Brain Dev. 2015 Aug;37(7):669-76. doi: 10.1016/j.braindev.2014.10.006. Epub 2014 Oct 31. Brain Dev. 2015. PMID: 25459970

2

[Soluble adhesion molecules in muscular dystrophy].

Saito T, Yamamoto Y, Shinno S. Saito T, et al. No To Hattatsu. 2002 Jul;34(4):326-9. No To Hattatsu. 2002. PMID: 12134684 Japanese.

3

Coagulation system activated in Duchenne muscular dystrophy patients with cardiac dysfunction.

Saito T, Yamamoto Y, Matsumura T, Nozaki S, Fujimura H, Shinno S. Saito T, et al. Brain Dev. 2005 Sep;27(6):415-8. doi: 10.1016/j.braindev.2004.11.001. Epub 2004 Dec 15. Brain Dev. 2005. PMID: 16122628

4

Tracheo-arterial fistula in tracheostomy patients with Duchenne muscular dystrophy.

Saito T, Sawabata N, Matsumura T, Nozaki S, Fujimura H, Shinno S. Saito T, et al. Brain Dev. 2006 May;28(4):223-7. doi: 10.1016/j.braindev.2005.08.002. Epub 2005 Dec 20. Brain Dev. 2006. PMID: 16368206

5

Cardiac troponin I for accurate evaluation of cardiac status in myopathic patients.

Matsumura T, Saito T, Fujimura H, Shinno S. Matsumura T, et al. Among authors: saito t. Brain Dev. 2007 Sep;29(8):496-501. doi: 10.1016/j.braindev.2007.01.009. Epub 2007 Mar 21. Brain Dev. 2007. PMID: 17376624 Clinical Trial.

6

Serum levels of vascular endothelial growth factor elevated in patients with muscular dystrophy.

Saito T, Yamamoto Y, Matsumura T, Fujimura H, Shinno S. Saito T, et al. Brain Dev. 2009 Sep;31(8):612-7. doi: 10.1016/j.braindev.2008.09.008. Epub 2008 Nov 5. Brain Dev. 2009. PMID: 18980821

7

Valproic acid increases SMN2 expression and modulates SF2/ASF and hnRNPA1 expression in SMA fibroblast cell lines.

Harahap IS, Saito T, San LP, Sasaki N, Gunadi, Nurputra DK, Yusoff S, Yamamoto T, Morikawa S, Nishimura N, Lee MJ, Takeshima Y, Matsuo M, Nishio H. Harahap IS, et al. Among authors: saito t. Brain Dev. 2012 Mar;34(3):213-22. doi: 10.1016/j.braindev.2011.04.010. Epub 2011 May 11. Brain Dev. 2012. PMID: 21561730

8

Efficacy and tolerance of gastrostomy feeding in Japanese muscular dystrophy patients.

Mizuno T, Komaki H, Sasaki M, Takanoha S, Kuroda K, Kon K, Mamiya S, Yoshioka M, Yatabe K, Mikata T, Ishihara T, Nakajima T, Watanabe H, Konagaya M, Mitani M, Konishi T, Tokita Y, Fukuda K, Tatara K, Maruta K, Imamura S, Shimazaki R, Ishikawa K, Saito T, Shinno S. Mizuno T, et al. Among authors: saito t. Brain Dev. 2012 Oct;34(9):756-62. doi: 10.1016/j.braindev.2011.11.012. Epub 2011 Dec 26. Brain Dev. 2012. PMID: 22204944

9

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.

10

SMA screening system using dried blood spots on filter paper: application of COP-PCR to the SMN1 deletion test.

Kato N, Sa'Adah N, Ar Rochmah M, Harahap NI, Nurputra DK, Sato H, Sadewa AH, Astuti I, Haryana SM, Saito T, Saito K, Nishimura N, Nishio H, Takeuchi A. Kato N, et al. Among authors: saito k, saito t. Kobe J Med Sci. 2015 Jan 19;60(4):E78-85. Kobe J Med Sci. 2015. PMID: 25791416 Free article.

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